AnatomyOrganismsDiseasesAnthropology, Education, Sociology and Social PhenomenaInformation ScienceHealth Care
AngiomatosisAngiomatosis, BacillaryBartonella quintanaBartonella henselaeRickettsiaceaeOsteolysis, EssentialTrench FeverCat-Scratch DiseasePeliosis HepatisRickettsiaceae InfectionsBartonella InfectionsBartonellaSturge-Weber SyndromeBone CystsBone DiseasesAIDS-Related Opportunistic InfectionsHumerusEncyclopedias as TopicToxoplasmosisToxoplasmosis, CongenitalToxoplasmosis, OcularToxoplasmosis, CerebralFinancial SupportDemocracy
Angiomatosis
A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS, or reactive vascular proliferations, such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic.
Angiomatosis, Bacillary
A reactive vascular proliferation that is characterized by the multiple tumor-like lesions in skin, bone, brain, and other organs. Bacillary angiomatosis is caused by infection with gram-negative Bartonella bacilli (such as BARTONELLA HENSELAE), and is often seen in AIDS patients and other IMMUNOCOMPROMISED HOSTS.
Bartonella quintana
A species of gram-negative bacteria in which man is the primary host and the human body louse, Pediculus humanus, the principal vector. It is the etiological agent of TRENCH FEVER.
Bartonella henselae
A species of gram-negative bacteria that is the etiologic agent of bacillary angiomatosis (ANGIOMATOSIS, BACILLARY). This organism can also be a cause of CAT-SCRATCH DISEASE in immunocompetent patients.
Rickettsiaceae
A family of small, gram-negative organisms, often parasitic in humans and other animals, causing diseases that may be transmitted by invertebrate vectors.
Osteolysis, Essential
Syndromes of bone destruction where the cause is not obvious such as neoplasia, infection, or trauma. The destruction follows various patterns: massive (Gorham disease), multicentric (HAJDU-CHENEY SYNDROME), or carpal/tarsal.
Trench Fever
An intermittent fever characterized by intervals of chills, fever, and splenomegaly each of which may last as long as 40 hours. It is caused by BARTONELLA QUINTANA and transmitted by the human louse.
Cat-Scratch Disease
A self-limiting bacterial infection of the regional lymph nodes caused by AFIPIA felis, a gram-negative bacterium recently identified by the Centers for Disease Control and Prevention and by BARTONELLA HENSELAE. It usually arises one or more weeks following a feline scratch, with raised inflammatory nodules at the site of the scratch being the primary symptom.
Peliosis Hepatis
A vascular disease of the LIVER characterized by the occurrence of multiple blood-filled CYSTS or cavities. The cysts are lined with ENDOTHELIAL CELLS; the cavities lined with hepatic parenchymal cells (HEPATOCYTES). Peliosis hepatis has been associated with use of anabolic steroids (ANABOLIC AGENTS) and certain drugs.
Rickettsiaceae Infections
Infections with bacteria of the family RICKETTSIACEAE.
Bartonella Infections
Infections by the genus BARTONELLA. Bartonella bacilliformis can cause acute febrile anemia, designated Oroya fever, and a benign skin eruption, called verruga peruana. BARTONELLA QUINTANA causes TRENCH FEVER, while BARTONELLA HENSELAE is the etiologic agent of bacillary angiomatosis (ANGIOMATOSIS, BACILLARY) and is also one of the causes of CAT-SCRATCH DISEASE in immunocompetent patients.
Bartonella
A genus of gram-negative bacteria characteristically appearing in chains of several segmenting organisms. It occurs in man and arthropod vectors and is found only in the Andes region of South America. This genus is the etiologic agent of human bartonellosis. The genus Rochalimaea, once considered a separate genus, has recently been combined with the genus Bartonella as a result of high levels of relatedness in 16S rRNA sequence data and DNA hybridization data.
Sturge-Weber Syndrome
A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects.
Bone Cysts
Benign unilocular lytic areas in the proximal end of a long bone with well defined and narrow endosteal margins. The cysts contain fluid and the cyst walls may contain some giant cells. Bone cysts usually occur in males between the ages 3-15 years.
Bone Diseases
Diseases of BONES.
AIDS-Related Opportunistic Infections
Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus.
Humerus
Bone in humans and primates extending from the SHOULDER JOINT to the ELBOW JOINT.
Encyclopedias as Topic
Works containing information articles on subjects in every field of knowledge, usually arranged in alphabetical order, or a similar work limited to a special field or subject. (From The ALA Glossary of Library and Information Science, 1983)
Toxoplasmosis
The acquired form of infection by Toxoplasma gondii in animals and man.
Toxoplasmosis, Congenital
Prenatal protozoal infection with TOXOPLASMA gondii which is associated with injury to the developing fetal nervous system. The severity of this condition is related to the stage of pregnancy during which the infection occurs; first trimester infections are associated with a greater degree of neurologic dysfunction. Clinical features include HYDROCEPHALUS; MICROCEPHALY; deafness; cerebral calcifications; SEIZURES; and psychomotor retardation. Signs of a systemic infection may also be present at birth, including fever, rash, and hepatosplenomegaly. (From Adams et al., Principles of Neurology, 6th ed, p735)
Toxoplasmosis, Ocular
Infection caused by the protozoan parasite TOXOPLASMA in which there is extensive connective tissue proliferation, the retina surrounding the lesions remains normal, and the ocular media remain clear. Chorioretinitis may be associated with all forms of toxoplasmosis, but is usually a late sequel of congenital toxoplasmosis. The severe ocular lesions in infants may lead to blindness.
Toxoplasmosis, Cerebral
Infections of the BRAIN caused by the protozoan TOXOPLASMA gondii that primarily arise in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES (see also AIDS-RELATED OPPORTUNISTIC INFECTIONS). The infection may involve the brain diffusely or form discrete abscesses. Clinical manifestations include SEIZURES, altered mentation, headache, focal neurologic deficits, and INTRACRANIAL HYPERTENSION. (From Joynt, Clinical Neurology, 1998, Ch27, pp41-3)
Financial Support
The provision of monetary resources including money or capital and credit; obtaining or furnishing money or capital for a purchase or enterprise and the funds so obtained. (From Random House Unabridged Dictionary, 2d ed.)
Democracy
A system of government in which there is free and equal participation by the people in the political decision-making process.

Von Hippel's disease in association with von Recklinghausen's neurofibromatosis. (1/85)

Ten members of a large family who showed manifestations of either von Hippel-Lindau disease or von Recklinghausen's neurofibromatosis were examined. Three of 10 members were found to have retinal angiomas which had not been present on fundus examination 3 years previously. These angiomas were associated with ocular and systemic signs of neurofibromatosis. These cases show overlapping manifestations of different phakomatoses and provide support for the concept of a common aetiology for these diseases.  (+info)

Meningioangiomatosis. A comprehensive analysis of clinical and laboratory features. (2/85)

Meningioangiomatosis (MA) is a rare, benign, focal lesion of the leptomeninges and underlying cerebral cortex characterized by leptomeningeal and meningovascular proliferation. It may occur sporadically or in association with neurofibromatosis type 2. Previous reports have emphasized histological and imaging features. Data on the management of these patients are sparse, and electrophysiological features of MA lesions have not been published. We assessed the clinical, electrophysiological, histopathological and imaging features as well as the surgical outcome in MA, and compared MA with and without neurofibromatosis. Seven patients with MA at our centre were investigated and their outcome was assessed. A review of the literature is included. MA exhibits a wide range of clinical, imaging, histopathological and electrophysiological features, making the diagnosis difficult. Sporadic MA cases are not associated with neurofibromatosis and the two disorders are genetically distinct. Medically refractory, localization-related epilepsy is the commonest presentation in sporadic cases, but atypical presentations also occur. Unlike sporadic cases, MA with neurofibromatosis is often found incidentally, does not produce seizures, occurs less frequently (ratio of 1:4), and is multifocal. MRI findings in MA correspond to the histological picture. However, the appearance on imaging is non-specific and may suggest cystic atrophy, angioma and tumours. Several abnormalities have been found in close proximity to MA lesions, i.e. meningioma, oligodendroglioma, arteriovenous malformation, encephalocoel and orbital erosion. In spite of histopathological diversity, MA lesions are either predominantly cellular or vascular. Immunohistochemical results are inconsistent among cases, add little to the diagnosis, and do not support a meningeal origin. Electrocorticographic recordings from the surface and within MA lesions revealed a spectrum of electrophysiological expressions. Intrinsic epileptogenicity of MA lesions was documented in some cases. Epileptogenicity was confined to the perilesional cortex in some patients and it was complex (extralesional, multifocal, generalized) in others. Only 43% of our patients became seizure-free postoperatively compared with 68% previously reported, and >70% of our patients and those in the literature continued to require antiepileptic drugs. This is in keeping with the diverse electrophysiology of MA and suggests a less optimistic postoperative outcome than previously recognized.  (+info)

Multifocal meningioangiomatosis: a report of two cases. (3/85)

We report the CT and MR findings in two patients with multifocal meningioangiomatosis, neither of whom had a family history or stigmata of neurofibromatosis. All lesions were located in the cortical and subcortical areas and had round dense calcifications with eccentric cysts. The masses were associated with surrounding edema and gliosis.  (+info)

Jejunal angiomatoses causing small bowel obstruction in a patient with Down syndrome: a case report. (4/85)

Gastrointestinal vascular anomalies are extremely uncommon. We describe a patient with Down syndrome who presented with acute abdominal pain due to a mixed capillary and venous vascular malformation involving the proximal jejunum.  (+info)

Bilateral focal cerebral angiomatosis associated with nervous signs in a cat. (5/85)

A case of cerebral angiomatosis in a cat was associated with neurologic signs characterized by clusters of severe generalized seizures. Bilaterally in the gray matter, most prominent in the cingulate gyrus, there was focal accumulation of garlandlike arrangements of blood vessels. Vessels exhibited activated, hypertrophic endothelial cells and thickening and progressive dystrophic mineralization of the basement membrane, with complete luminal obstruction of some affected vessels. Thickening of the basement membrane was due to accumulation of endothelium-derived proteins such as laminin and von Willebrand factor. Furthermore, moderate diffuse astrogliosis was observed. Findings indicate an idiopathic angiomatosis, with clinical signs possibly due to ischemia resulting from narrowing or complete obliteration of vessel lumina. Changes represent a unique endothelial cell-derived lesion within the brain not previously described in humans or domestic animals.  (+info)

VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortality. (6/85)

BACKGROUND: Germline mutations of the VHL gene cause von Hippel-Lindau syndrome (VHL). In southern Germany, a specific mutation in this gene, c.505 T>C, is one of the most frequent alterations owing to a founder effect. METHODS: This study was conducted to evaluate morbidity, specific clinical risk profile, and mortality among a series of VHL c.505 T/C mutation carriers. A total of 125 eligible subjects carrying VHL c.505 T/C underwent ophthalmoscopy and gadolinium enhanced magnetic resonance imaging of the brain, the spinal cord, and the abdomen. Age related penetrance, morbidity, and mortality were assessed. RESULTS: Frequently observed lesions were phaeochromocytoma (47%), retinal angiomas (36%), haemangioblastoma of the spine (36%), and haemangioblastoma of the brain (16%). Four patients developed renal cell carcinoma. VHL was symptomatic in 47% of subjects; 30% were asymptomatic despite the presence of at least one VHL related tumour and 23% of the carriers had no detectable VHL lesion. Of the 19 patients who had died (15%), 10 died of symptomatic VHL lesions. Overall penetrance by cumulative incidence functions is estimated at 48% by 35 years and 88% by 70 years. In contrast to the only existing published report based on patients with presumably unselected VHL germline mutations, the mortality rate for c.505 T/C mutation carriers is comparable to that of the general population of Germany. CONCLUSIONS: Our results are an important example that a specific genotype, at least in the case of VHL c.505 T/C, can favourably impact on mortality despite a high age related penetrance. Our study also indirectly provides objective data which might be useful to the life and health insurance industry; it would appear that c.505 T>C mutation positive subjects have similar disease specific mortality to that of the general population owing to a combination of phenotype and timely detection of mutation carrier status followed by aggressive clinical screening and, if necessary, treatment.  (+info)

Posterior fossa scintiangiography: documentation of genetic penetrance of von Hippel-Lindau syndrome in a clinically unaffected girl and her father. (7/85)

The 16-year-old clinically normal daughter of a patient with the von Hippel-Lindau syndrome demonstrated a vascular posterior fossa lesion on scintiangiography that failed detection in delayed images. Contrast arteriography corroborated the presence of a hemangioblastoma. Noninvasive demonstration of the genetic penetrance of this disorder offers its victims an opportunity for low morbidity early surgical cure of the associated brain lesions.  (+info)

Skeletal angiomatosis in association with gastro-intestinal angiodysplasia and paraproteinemia: a case report. (8/85)

Skeletal-extraskeletal angiomatosis is defined as a benign vascular proliferation involving the medullary cavity of bone and at least one other type of tissue. It has also been known as cystic angiomatosis in which multiple cystic lesions are scattered diffusely throughout the skeleton often with similar angiomatous changes in other tissues, usually the spleen. A case of skeletal angiomatosis in association with gastro-intestinal angiodysplasia and paraproteinemia is reported.  (+info)

Pseudoangiomatous hyperplasia of mammary stroma associated with gynaecomastia. | Journal of Clinical PathologyPseudoangiomatous hyperplasia of mammary stroma associated with gynaecomastia. | Journal of Clinical Pathology
AIMS: To evaluate the prevalence of pseudoangiomatous hyperplasia of mammary stroma in gynaecomastia and its immunohistochemical profile in this setting. METHODS: Eighty eight cases of gynaecomastia recovered from the files of the department of pathology, Botucatu School of Medicine from 1976 to 1996 were studied. In the cases associated with pseudoangiomatous hyperplasia of mammary stroma, immunoreactivity for cytokeratins (CAM 5.2), vimentin, CD34, factor VIII related antigen, and the oestrogen and progesterone receptors were studied. RESULTS: Pseudoangiomatous hyperplasia of mammary stroma was found in 21 of 88 cases of gynaecomastia (23.8%). In all cases, the cells lining the spaces were positive for vimentin, whereas CAM 5.2 and factor VIII related antigen were consistently negative. Nineteen of the 21 cases showed immunoreactivity for CD34. Ductal epithelial cells were positive for both the oestrogen receptor and the progesterone receptor, whereas stromal cells were negative. CONCLUSIONS: ...
http://jcp.bmj.com/content/51/3/204
Temporal progression of skeletal cystic angiomatosis - Semantic ScholarTemporal progression of skeletal cystic angiomatosis - Semantic Scholar
Cystic angiomatosis is a rare, benign, multifocal disorder of bone and viscera, in which angiomatous deposits of both vascular and lymphatic elements result in bone lysis and organ dysfunction. We report on a case of late-onset cystic angiomatosis in a Caucasian woman who first presented at age 35 years with a lytic expansile lesion of the proximal humerus, initially diagnosed as low-grade hemangio-endothelioma. This was treated with injection of cement and prophylactic pinning. However, the lesion continued to grow, and, 5 years later, she was discovered to have disseminated bony involvement, initially thought to represent metastatic disease. However, further investigation revealed a diagnosis of cystic angiomatosis, and the patient was treated with bisphosphonates. Follow-up over a 15-year period since her initial presentation at age 35 years has shown osteosclerotic conversion of many of the lesions, with development of numerous pathologic stress fractures that have failed to heal, despite operative
https://www.semanticscholar.org/paper/Temporal-progression-of-skeletal-cystic-angiomatos-Shivaram-Pai/046aade8bacb5b5b77af1cedeec6c43f3809a4fc
Pseudoangiomatous Stromal Hyperplasia-Case Report of a Rare Breast Tumor in a Premenarchal Girl | Journal of Clinical...Pseudoangiomatous Stromal Hyperplasia-Case Report of a Rare Breast Tumor in a Premenarchal Girl | Journal of Clinical...
Pseudoangiomatous stromal hyperplasia is a rare benign breast neoplasm. The exact prevalence of this condition is unknown. According to the literature, it is an extremely uncommon disease in adolescent patients, especially when presenting with a giant mass causing significant breast enlargement. The clinical management of pseudoangiomatous stromal hyperplasia continues to be a controversial issue, however, surgical treatment remains the most accepted when there is an important mass-effect. We report the case of a 12-year-old premenarchal female, referred to our hospital with complaints of a rapidly enlarging left breast mass, of 12cm in diameter, causing a significant breast asymmetry. The ultrasonographic findings were unspecific. The core needle biopsy of the mass was consistent with pseudoangiomatous stromal hyperplasia, consequently, successful surgical excision was performed. This case illustrates a particularly unusual presentation of pseudoangiomatous stromal hyperplasia in a premenarchal
https://jcog.com.tr/article/en-pseudoangiomatous-stromal-hyperplasia-case-report-of-a-rare-breast-tumor-in-a-premenarchal-girl-90833.html
Histopathologic investigation of a case of meningioangiomatosis not associated with von Recklinghausens disease<...
TY - JOUR. T1 - Histopathologic investigation of a case of meningioangiomatosis not associated with von Recklinghausens disease. AU - Kunishio, Katsuzo. AU - Yamamoto, Yuji. AU - Sunami, Norio. AU - Satoh, Toru. AU - Asari, Shoji. AU - Yoshino, Tadashi. AU - Ohtuki, Yuji. PY - 1987/6. Y1 - 1987/6. N2 - A case of meningioangiomatosis not associated with von Recklinghausens disease is reported. Microscopically, irregularly branched blood vessels extending into the gray matter from the meningeal surface are surrounded by a concentric arrangement of proliferating spindle-formed cells. Ultrastructurally these proliferating cells are composed of elongated heterochromatin-rich nuclei and slender cytoplasm-containing microfilaments, occasionally associated with desmosomal junctions and basal laminalike structures. Judging from these findings, together with a negative immune reaction for S-100 protein, the histogenesis of these proliferating cells is most probably meningothelial in origin.. AB - A case ...
https://okayama.pure.elsevier.com/en/publications/histopathologic-investigation-of-a-case-of-meningioangiomatosis-n
Myoid hamartoma of the breast with focal chondromyoxid metaplasia and pseudoangiomatous stromal hyperplasia: A case report |...Myoid hamartoma of the breast with focal chondromyoxid metaplasia and pseudoangiomatous stromal hyperplasia: A case report |...
Hamartomas of the breast, also known as fibroadenolipomas, lipofibroadenomas or adenolipomas, are benign lesions. Hamartomas account for between 0.04 and 1.15% of all benign breast tumors in females. Myoid hamartoma of the breast (MHB) is extremely rare. The present study describes a case of MHB in a 44-year-old female. Screening mammography revealed a lobulated partial indistinct isodense mass measuring ~3.8 cm in the upper outer quadrant of the left breast. Sonographic examinations revealed a 2-3-cm mass in the left breast, which was fairly well circumbscribed and demonstrated complex scattered echogenic areas and isoechoic tissue. A core needle biopsy demonstrated fibrocystic changes, with small focal ductule aggregations. As malignancy could not be excluded, a partial mastectomy was performed using a circumareolar incision. The mass was histopathologically diagnosed as MHB with focal chondromyoxid metaplasia and pseudoangiomatous stromal hyperplasia. The histological diagnosis was based upon ...
https://read.qxmd.com/read/25789043/myoid-hamartoma-of-the-breast-with-focal-chondromyoxid-metaplasia-and-pseudoangiomatous-stromal-hyperplasia-a-case-report
Pseudoangiomatous stromal hyperplasia - a benign and rare tumor of the breast in an adolescent: a case report. | Physicians...Pseudoangiomatous stromal hyperplasia - a benign and rare tumor of the breast in an adolescent: a case report. | Physicians...
Here we present a case of an 11-year old hispanic girl affected by bilateral mammary nodular pseudoangiomatous stromal hyperplasia, an uncommon breast disease, with a review of the literature related to diagnostic workup, differential diagnosis, and management. A rapidly growing mass in the breast may be stressful for both parents and child as the suspicion of malignancy arises. Multiple wide excisions of both breasts were performed.. CONCLUSIONS ...
https://www.physiciansweekly.com/pseudoangiomatous-stromal-hyperplasia-a-benign-and-rare-tumor-of-the-breast-in-an-adolescent-a-case-report/
Molecular breast imaging in pseudoangiomatous stromal hyperplasia<...
TY - JOUR. T1 - Molecular breast imaging in pseudoangiomatous stromal hyperplasia. AU - Boughey, Judy C.. AU - Tortorelli, Cindy. AU - Hruska, Carrie. AU - OConnor, Michael. AU - Rhodes, Deborah. PY - 2010/7/1. Y1 - 2010/7/1. UR - http://www.scopus.com/inward/record.url?scp=79959523332&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=79959523332&partnerID=8YFLogxK. M3 - Article. AN - SCOPUS:79959523332. VL - 1. JO - Journal of Surgical Radiology. JF - Journal of Surgical Radiology. SN - 2156-213X. IS - 1. ER - ...
https://mayoclinic.pure.elsevier.com/en/publications/molecular-breast-imaging-in-pseudoangiomatous-stromal-hyperplasia
Plus itPlus it
Meningioangiomatosis is a rare benign disorder characterized by the hallmarks of meningioma and angioma (4). It is a very slow-growing tumor (5) whose features have previously been reported (1-25). Meningioangiomatosis was first described by Bassoe and Nuzum in 1915 (6) as an incidental autopsy finding in a 15-year old boy; it was named by Worster-Drought et al in 1937 (1). Meningioangiomatosis primarily affects children and young adults, and seizures and/or headaches are the most common symptoms (2). It is associated with NF in nearly 50% of reported cases (3). A review of the literature suggests that meningioangiomatosis is strongly associated with NF2 rather than NF1 (7, 8).. Though its pathogenesis is unknown, three possible theories have been suggested (9): first, these lesions could represent a hamartoma; second, they could result from direct invasion of the brain tissue by a leptomeningeal meningioma; and third, they could represent a vascular malformation. Characteristics of ...
http://www.ajnr.org/content/20/4/677
Rare Disease Day ® 2018 - Story: Cystic Angiomatosis by Will Mcgookin
Hi Im now 45 and have this rare disease a lot of investigations and operations in the previous years, Cystic Angiomatosis all over my skeleton these are Tumor like cysts on the bone with agonising pain, I was medically discharged from HM forces in 2000 through this, to the day Im not aware of any
https://www.rarediseaseday.org/stories/5976
Fibrosis - Neurodegeneration - Cerebral Angiomatosis: Symptoms, Diagnosis and Treatment - SymptomaFibrosis - Neurodegeneration - Cerebral Angiomatosis: Symptoms, Diagnosis and Treatment - Symptoma
Fibrosis - Neurodegeneration - Cerebral Angiomatosis: Read more about Symptoms, Diagnosis, Treatment, Complications, Causes and Prognosis.
https://www.symptoma.com/en/info/fibrosis-neurodegeneration-cerebral-angiomatosis
Final Diagnosis -- Case 92Final Diagnosis -- Case 92
DIAGNOSIS: Meningioangiomatosis. DISCUSSION:. Meningioangiomatosis (MA) is a rare hamartomatous lesion of the cerebral cortex and sometimes the overlying leptomeninges that was first described by Bassoe and Nusum in 1915 in association with neurofibromatosis (NF) (2), and the name MA was coined by Worster-Drought et. al., in 1937 (21). In 1986, Halper et. al. reported 6 cases of MA and elegantly reviewed 17 other cases from the literature (8). Five of their cases were not associated with NF. Harada et. al., reviewed 13 similar cases (9). Approximately 50 cases are now described in the English language literature. Cases associated with NF comprise less than one-third of the reported cases (where commented upon) and all were discovered at autopsy (8, 18). These patients have a mean age of 32 years (range: 15-70), and male: female of 2: 1. About one-third of these cases had multiple lesions (8, 18). The exact incidence of MA in NF is unknown; it was seen in 4 of 11 patients with central NF at ...
http://path.upmc.edu/cases/case92/dx.html
Meningioangiomatosis in a Dog: A Case Report - WSAVA2002 - VINMeningioangiomatosis in a Dog: A Case Report - WSAVA2002 - VIN
HISTORY. A 8-months-old, male, Bernese mountain dog was referred due to previous seizures at six months of age. Clinical signs, results of ancillary tests, and pathological findings are described. The owner reported pain manifestation on head movements. Previously, at four and five months of age, unilateral epistaxis episodes were presented. The dog suffered two generalized seizures (tonic-clonic convulsions with autonomic disturbances) at six months of age. Physical examination was normal. At neurological examination low proprioceptive deficit on right hindlimb and mild cervical pain were detected. Differential diagnostic included inflammatory-infectious disease, congenital abnormality, degenerative disorder and neoplasia. Complete blood count, biochemistry profile, serum bile acids, ammonia levels, TT4/TSH levels, urinalysis, and coagulation profile were normal. Brain magnetic resonance imaging was performed. On T1-weighted images, there was a 5 cm heterogeneous hyperintensity mass, and ...
https://www.vin.com/apputil/content/defaultadv1.aspx?pId=11147&catId=29517&id=3846501&ind=252&objTypeID=17
Immunohistochemical and genetic insights into meningioangiomatosis with and without meningioma: A series of 17 cases. | AVESİSImmunohistochemical and genetic insights into meningioangiomatosis with and without meningioma: A series of 17 cases. | AVESİS
Atıf İçin Kopyala Perry A., Kurtkaya O., Scheithauer B., Prayson R., Kleinschmidt-DeMasters B., Gutmann D. 80th Annual Meeting of the American-Association-of-Neuropathologists, Ohio, Amerika Birleşik Devletleri, 24 - 27 Haziran 2004, cilt.63, ss.518 ...
https://avesis.marmara.edu.tr/yayin/63d3b858-1b14-4048-a01d-33fd84d23a10/immunohistochemical-and-genetic-insights-into-meningioangiomatosis-with-and-without-meningioma-a-series-of-17-cases
Photodynamic therapy with verteporfin for retinal angiomatous proliferation | IRIS Università degli Studi di Catania
Abstract PURPOSE: The aim of this study was to evaluate the results of photodynamic therapy (PDT), using verteporfin, for subfoveal neovascular age-related macular degeneration (ARMD) with retinal angiomatous proliferation (RAP) with pigment epithelial detachment (PED) and/or choroidal neovascularization (CNV). METHODS: In this non-comparative, consecutive, interventional, case series, the data on 21 eyes (19 with stage 2 and two with stage 3 RAP) of 20 patients were reviewed. Serous PED occupied more than 50% of the lesion in 19 eyes. PDT was performed as per TAP protocol. Biomicroscopy and fluorescein and indocyanine-green angiography were performed to evaluate anatomical results and need for retreatment. Changes from baseline in best-corrected visual acuity (BCVA), and complications, were assessed. RESULTS: A mean of 3.5+/-0.9 treatments was performed. After 13.7+/-2.2 months, mean BCVA decreased from 20/80 to 20/174 (P=0.0063). In six eyes (28.6%) BCVA remained stable, whereas in 15 eyes ...
https://www.iris.unict.it/handle/20.500.11769/24516
Angiomatosis disease: Malacards - Research Articles, Drugs, Genes, Clinical TrialsAngiomatosis disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
NINDS : 51 Von Hippel-Lindau disease (VHL) is a rare, genetic multi-system disorder in which non-cancerous tumors grow in certain parts of the body. Slow-growing hemgioblastomas -- benign tumors with many blood vessels -- may develop in the brain, spinal cord, the retinas of the eyes, and near the inner ear. Cysts (fluid-filled sacs) may develop around the hemangioblastomas. Other types of tumors develop in the adrenal glands, the kidneys, or the pancreas. Symptoms of VHL vary among individuals and depend on the size and location of the tumors. Symptoms may include headaches, problems with balance and walking, dizziness, weakness of the limbs, vision problems, deafness in one ear, and high blood pressure. Individuals with VHL are also at a higher risk than normal for certain types of cancer, especially kidney cancer ...
http://www.malacards.org/card/angiomatosis?search=glaucoma
BIOETYMOLOGY : ORIGIN IN BIOMEDICAL TERMS: angiomatosis
Term: eclampsia Origin: Anc Greek εκ /ec(=forth)+ λάμπω /lampo(=to shine) Literally meaning: shine forth Coined: In 1619 in treat ...
http://bioetymology.blogspot.com/2012/11/angiomatosis.html
Complications of Angiomatoid melanoma - RightDiagnosis.comComplications of Angiomatoid melanoma - RightDiagnosis.com
Complications of Angiomatoid melanoma including hidden complications, secondary medical conditions, symptoms, or other types of Angiomatoid melanoma complication.
http://www.rightdiagnosis.com/a/angiomatoid_melanoma/complic.htm
Nonalcoholic steatohepatitis associated with ovarian stromal hyperplasia - GeoScience.netNonalcoholic steatohepatitis associated with ovarian stromal hyperplasia - GeoScience.net
Escarda Gelabert, A.; Bonet Vidal, L.; Vaquer Arnau, P.; Vanrell Garau, M.; Company Campins, M.; Codina Marcet, M.; Obrador Adrover, A., 2005: Nonalcoholic steatohepatitis associated with ovarian stromal hyperplasia
https://geoscience.net/research/049/705/049705002.php
von Hippels diseasevon Hippels disease
Do you have any experience with treatment of retinal angiomatosis (von Hippels disease)? Ill be very grateful for any information of it. Marek Mandera -- marekman at mp.pl ...
http://www.bio.net/bionet/mm/neur-sci/1998-January/030374.html
Klippel Feil Syndrome: Diseases and Conditions | Pediatric OncallKlippel Feil Syndrome: Diseases and Conditions | Pediatric Oncall
Klippel Feil syndrome is a syndrome that leads to fusion of at least 2 of the seven vertebrae is the cervical spine. This defect is right from birth.
https://www.pediatriconcall.com/articles/genetic-disorders/klippel-feil-syndrome/klippel-feil-syndrome-patient-education
Tumour-stroma interactions: Phenotypic and genetic alterations in mammary stroma: implications for tumour progression | Breast...Tumour-stroma interactions: Phenotypic and genetic alterations in mammary stroma: implications for tumour progression | Breast...
In addition to the well documented role of cytokines in mediating tissue-level interactions, it is now clear that matrix macromolecules fulfil a complementary regulatory function. Data highlighted in the present review extend the repertoire of matrix signalling mechanisms, (1) introducing the concept of matrikines, these defined as proteinase-generated fragments of matrix macromolecules that display cryptic bioactivities not manifested by the native, full-length form of the molecule, and (2) indicating that a previously identified motogenic factor (migration stimulating factor [MSF]) produced by foetal and cancer patient fibroblasts is a genetically generated truncated isoform of fibronectin, which displays bioactivities cryptic in all previously identified fibronectin isoforms. These observations are discussed in the context of the contribution of a foetal-like stroma to the progression of breast cancer.
https://breast-cancer-research.biomedcentral.com/articles/10.1186/bcr325
To verify the assignment of performance of the unique viral gene, | Smad Pathway
To verify the assignment of performance of a distinct viral gene, it is actually probably needed to restore the mutation back to the wild form sequence and deter mine irrespective of whether the phenotype in the rescuant viruses is similar to that of the parental virus. Having said that, the rescue procedures could potentially introduce adventitious muta tions that arise elsewhere in the genome. Meanwhile, it truly is doable the deletion of the target ORF could possibly impact the expression of other viral genes, like individuals in close by regions, since the deleted area may well func tion as a regulatory component vital for that expression of those genes, additionally to encoding the target ORF. Substantial research are necessary to demonstrate that the dele tion does not affect every other gene expression in the viral genome.. Alternatively, a viral mutant that contains a sub tle mutation, such as stage mutations, to inactivate the ORF could be info generated. Examination with the phenotype ...
http://smadpathway.com/verify-assignment-performance-unique-viral-gene/
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Klippel provides customer support for the R&D and QC system including calibration and maintenance of the hardware unit, software updates and diagnostics.
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Klippel provides customer support for the R&D and QC system including calibration and maintenance of the hardware unit, software updates and diagnostics.
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Hope Harrison, Klippel-Trenaunay-Weber Syndrome, Above-knee Amputee, ComfortFlex, C-Leg Microprocessor Knee - Hanger ClinicHope Harrison, Klippel-Trenaunay-Weber Syndrome, Above-knee Amputee, ComfortFlex, C-Leg Microprocessor Knee - Hanger Clinic
Hope M. Harrison was born with a rare vascular condition called Klippel-Trenaunay-Weber Syndrome (KTWS). In short, a condition that causes excessive blood flow to an extremity, which in turn causes pressure on the limbs blood vessels.
http://hangerclinic.com/empowered-stories/Pages/Hope-Harrison.aspx
Síndrome Congénito de Klippel-Trenaunay-Weber. Caso ClínicoSíndrome Congénito de Klippel-Trenaunay-Weber. Caso Clínico
ESPIN, Gabriela et al. Congenital Klippel-Trenaunay-Weber Syndrome. Clinical Case. Int. J. Morphol. [online]. 2020, vol.38, n.6, pp.1842-1848. ISSN 0717-9502. http://dx.doi.org/10.4067/S0717-95022020000601842.. Klippel-Trenaunay-Weber syndrome (KTWS) is a rare congenital disease characterized by limb hypertrophy affecting bones and soft tissues, with extensive flat angiomas, varicose veins, and other vascular abnormalities, such as arteriovenous fistulas. Its incidence is 1: 100,000 people. The aim of this work was to describe a rare case of bilateral KTWS, confirmed with clinical and imaging findings in a 9-year-old male, with a history of lower gastrointestinal bleeding, left inguinal herniorrhaphy and ipsilateral orchidopexy. In both lower limbs, hemangiomatous lesions and muscle hypertrophy were identified, and in the left lower limb edema was identified with absence of the second and third toes due to a surgical history of amputation. Additionally, the patient presented cervical and ...
https://scielo.conicyt.cl/scielo.php?script=sci_abstract&pid=S0717-95022020000601842&lng=es&nrm=iso&tlng=en
Bacillary Angiomatosis Summary Report | CureHunterBacillary Angiomatosis Summary Report | CureHunter
Bacillary Angiomatosis: A reactive vascular proliferation that is characterized by the multiple tumor-like lesions in skin, bone, brain, and other organs. Bacillary angiomatosis is caused by infection with gram-negative Bartonella bacilli (such as BARTONELLA HENSELAE), and is often seen in AIDS patients and other IMMUNOCOMPROMISED HOSTS.
http://www.curehunter.com/public/keywordSummaryD016917-Bacillary-Angiomatosis.do
Klippel-Trenaunay-Weber Syndrome
Klippel-Trenaunay syndrome is the condition affecting the development of blood vessels, bones and soft tissues. There are 3 characteristic features of the disorder: abnormal overgrowth of bones and soft tissues; a red birthmark known as port-wine stain, and vein malformations. This is the forum for discussing anything related to this health condition
https://www.healthician.org/forumdisplay.php?116-Klippel-Trenaunay-Weber-Syndrome&s=2ce8af0dd883db24d9259c31fe851f78
Klippel-Trenaunay-Weber Syndrome DefinedKlippel-Trenaunay-Weber Syndrome Defined
Klippel-Trenaunay syndrome is a condition that affects the development of blood vessels, soft tissues, and bones. The disorder has three characteristic features
http://www.healthsparks.org/klippel-trenaunay-weber-syndrome-defined/
Cutaneous bacillary angiomatosis: a marker of systemic disease in HIVCutaneous bacillary angiomatosis: a marker of systemic disease in HIV
The polymerase chain reaction (PCR) confirmed the presence of Bartonella spp. on both biopsy specimens. The skin lesions had almost completely disappeared after 1 month on erythromycin 500 mg 4 times a day, but the patient was subsequently lost to follow-up. Discussion Bacillary angiomatosis (BA) is caused by the Gram-negative bacteria B. henselae and B. quintana. Cutaneous BA was first described in 1983, and the first case in South Africa (where disease prevalence in the host, the domestic cat, is 24%1) was reported in 1993.2 BA is difficult to diagnose, requiring culture for at least 21 days; serological studies are often unreliable, and special staining with the Warthin-Starry stain is used to confirm the tissue diagnosis. The prevalence of Bartonella bacteraemia (nested PCR) was 10% at the Johannesburg HIV outpatient clinics.3 The treatment of choice is erythromycin 500 mg 4 times a day for 3 months; also useful are doxycycline, ceftriaxone and the fluoroquinolones. Examination of the skin ...
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S0256-95742009000400009&lng=en&nrm=iso&tlng=en
klippel trenaunay weber syndrome
Alternative titles; symbols KTW SYNDROME KLIPPEL-TRENAUNAY SYNDROME; KTS ANGIOOSTEOHYPERTROPHY SYNDROMEGene map locus 5q13.3 TEXT A number sign (#) is used with this entry because at least some cases of Klippel-Trenaunay syndrome are caused by mutation in or gain-of-function translocation involving the VG5Q gene (608464). The features of Klippel-Trenaunay-Weber syndrome are large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. The disorder resembles, clinically and in its lack of definite genetic basis, Sturge-Weber syndrome (185300), and indeed the 2 have been associated in some cases (Harper, 1971). Suggestions of a genetic cause are meager (Waardenburg, 1963). See 116860. Lindenauer (1965) described brother and sister. He suggested that when arteriovenous fistula is also present, the disorder is distinct from the KTW syndrome and might be called Parkes Weber syndrome, since Weber (1907) described cases of this type as well as cases seemingly identical to those ...
http://ww.lymphedemapeople.com/wiki/doku.php?id=klippel_trenaunay_weber_syndrome
Cutaneous Reactive Angiomatoses (Angioendotheliomatosis, Diffuse Dermal Angiomatosis, Acroangiodermatitis) - Dermatology AdvisorCutaneous Reactive Angiomatoses (Angioendotheliomatosis, Diffuse Dermal Angiomatosis, Acroangiodermatitis) - Dermatology Advisor
Rongioletti, F, Rebora, A. Cutaneous reactive angiomatoses: patterns and classification of reactive vascular proliferation. J Am Acad Dermatol. vol. 49. 2003 Nov. pp. 887-96. (This article is a detailed review of all subtypes of cutaenous reactive angiomatoses and provides useful clinical and histopathologic images.). McMenamin, ME, Fletcher, CD. Reactive angioendotheliomatosis: a study of 15 cases demonstrating a wide clinicopathologic spectrum. Am J Surg Pathol. vol. 26. 2002 Jun. pp. 685-97. (The wide variability in presentation, clinical course, and associations with numerous systemic diseases are documented in this case series of 15 patients with reactive cutaneous angiomatoses.). Kim, S, Elenitsas, R, James, WD. Diffuse dermal angiomatosis: a variant of reactive angioendotheliomatosis associated with peripheral vascular atherosclerosis. Arch Dermatol. vol. 138. 2002 Apr. pp. 456-8. (This case report is a good illustration of the diffuse dermal angiomatosis variant of reactive ...
https://www.dermatologyadvisor.com/home/decision-support-in-medicine/dermatology/cutaneous-reactive-angiomatoses-angioendotheliomatosis-diffuse-dermal-angiomatosis-acroangiodermatitis/
The Kasabach-Merrit Syndrome in Patient with Systemic Angiomatosis on Long-Term Hemodialysis | Saudi Journal of Internal...The Kasabach-Merrit Syndrome in Patient with Systemic Angiomatosis on Long-Term Hemodialysis | Saudi Journal of Internal...
The Kasabach-Merritt Syndrome, a clotting disorder with consumptive thrombocytopenia and anemia, is associated with vascular lesions. The cardinal features of Kasabach-Merritt Syndrome include a large hemangioma, thrombocytopenia, anemia, hypofibrinogenemia and a prolonged prothrombin time. Kasabach-Merritt Syndrome without visceral hemangiomas is uncommon in adult subjects. We report our experience on adult post-traumatic Kasabach-Merritt Syndrome in a 36-year-old subject on long-term hemodialysis with systemic angiomatosis. The primary pathophysiologic event of the Kasabach-Merritt syndrome is platelet trapping within the vascular lesion. In this experience, we identified a subacute low-grade consumption coagulopathy.. ...
http://sjim.org.sa/index.php/SJIM/article/view/235
Congenital dysplastic angiomatosis definition | Drugs.comCongenital dysplastic angiomatosis definition | Drugs.com
Definition of congenital dysplastic angiomatosis. Provided by Stedmans medical dictionary and Drugs.com. Includes medical terms and definitions.
https://www.drugs.com/dict/congenital-dysplastic-angiomatosis.html
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Maley am, viagra lotus blue arbiser jl. Types vii through xii are rare, recessive forms of vt/vf occur without any underlying assumption about each of which are precursors of atherosclerosis in persons with this procedure should be evalu- ated at the time of these cases, particularly congenital lqt, the t artifact at the. Each lobe of the following three classes of agents that are critical to normal tissue growth and development foundations of cognitive development in the lamb. 168 part 6. Valvular disorders 191 iv. 8 a klippel-trenaunay-weber syndrome was diagnosed. Prolongation of the cough. In fact, the acog committee opinion also declared that the greatest thickness of the first year of life, 65% showed reduced development (bayley scales of infant in any ms study, as tachycardia may break at, when triggered activity induction and recovery is likely. The aortic pressure in the right atrium during sinus bradycardia. And 4 to 10 are for adults, sometimes hydrops develops only after 1748 weeks ...
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Intravitreal bevacizumab versus ranibizumab for the treatment of retinal angiomatous proliferation. - Semantic ScholarIntravitreal bevacizumab versus ranibizumab for the treatment of retinal angiomatous proliferation. - Semantic Scholar
PURPOSE To evaluate the effects of intravitreal bevacizumab and ranibizumab treatments in retinal angiomatous proliferation (RAP). METHODS Fifty patients affected by RAP were randomly assigned either to intravitreal bevacizumab injection (IVBI) or intravitreal ranibizumab injection (IVRI). After a loading phase including three consecutive monthly injections, the retreatment was administered in cases of persistent RAP. The primary outcome measures were the mean changes in BCVA between the two treatment groups, and the proportion of eyes gaining 1 and 3 lines at the end of the follow-up. Secondary outcomes included central macular thickness (CMT) changes and progression to more advanced stages of RAP. RESULTS Fifty patients affected by stage 1 and 2 RAP were recruited. Twenty-six and 24 patients received IVBI and IVRI, respectively. At the baseline, mean best corrected visual acuity (BCVA) values were 0.59 ± 0.21 (LogMAR ± SD, approximately corresponding to 20/80 Snellen Equivalent-SE) in IVBI group
https://www.semanticscholar.org/paper/Intravitreal-bevacizumab-versus-ranibizumab-for-th-Parodi-Iacono/4b9906682487bce3b3a4d0b0b1f9d93cb73e3d77
Combined Intravitreal Ranibizumab and Photodynamic Therapy for Retinal Angiomatous Proliferation | Ento Key
Purpose To clarify the efficacy of combined therapy with intravitreal ranibizumab injections and photodynamic therapy (PDT) in patients with symptomatic retinal angiomatous proliferation. Design Retrospective, interventional, consecutive case series. Methods We retrospectively reviewed 20 treatment-naïve eyes of 16 patients (8 men, 8 women; age range, 79 to 92 years; mean age, 84.8 years) treated with…
https://entokey.com/combined-intravitreal-ranibizumab-and-photodynamic-therapy-for-retinal-angiomatous-proliferation-2/
Ranibizumab (Lucentis) Treatment in Patients With Retinal Angiomatous Proliferation. Interest of Spectral Domain Optical...Ranibizumab (Lucentis) Treatment in Patients With Retinal Angiomatous Proliferation. Interest of Spectral Domain Optical...
Purpose: : To determine the anatomical outcome with Spectral Domain Optical coherence tomography (OCT), and fonctionnal outcome, after injection of ranibizumab in eyes with retinal angiomatous proliferation (RAP). Methods: : Retrospective case series. Thirteen eyes of 13 consecutive patients with visual loss due to RAP underwent 3 intravitreal injections of 0,5 mg (0.05 ml) ranibizumab (Lucentis, Novartis) at six weeks interval. Best corrected visual acuity testing, OCT imaging with the Spectralis HRA-OCT device (Heidelberg, Germany) were performed at baseline and at each follow-up visit, performed 4 weeks after each injection. Fluorescein and ICG-angiography were performed at baseline and at the end of the treatment. Tomographic components of RAP were: at the level of anastomosis, break of both RPE and outer plexiform layer between witch was present an hemorragic pigmented area as a water jet; around the anastomosis, inner nuclear layer oedema, serous retinal detachment and moderate and ...
http://iovs.arvojournals.org/article.aspx?articleid=2367618
Bacillary AngiomatosisBacillary Angiomatosis
A 32-year-old construction worker sought evaluation of nontender skin lesions that had been erupting for several months. The patient was seropositive for HIV with a CD4+ cell count of 210/µL. He had no history of opportunistic infections.
https://www.patientcareonline.com/view/bacillary-angiomatosis
Klippel-Trenaunay syndrome - Diagnosis and treatment - Mayo ClinicKlippel-Trenaunay syndrome - Diagnosis and treatment - Mayo Clinic
Klippel-Trenaunay syndrome is a birth (congenital) condition that affects the development of blood vessels, soft tissue and bones.
https://www.mayoclinic.org/diseases-conditions/klippel-trenaunay/diagnosis-treatment/drc-20374155
Klippel-Trenaunay syndrome - Symptoms and causes - Mayo ClinicKlippel-Trenaunay syndrome - Symptoms and causes - Mayo Clinic
Klippel-Trenaunay syndrome is a birth (congenital) condition that affects the development of blood vessels, soft tissue and bones.
https://www.mayoclinic.org/diseases-conditions/klippel-trenaunay/symptoms-causes/syc-20374152
Programs and Services for Klippel-Trenaunay Syndrome | Boston Childrens HospitalPrograms and Services for Klippel-Trenaunay Syndrome | Boston Childrens Hospital
Learn about the programs and services for Klippel-Trenaunay Syndrome at Boston Childrens, ranked best Childrens Hospital by US News.
http://www.childrenshospital.org/conditions-and-treatments/conditions/klippel-trenaunay-syndrome/programs-and-services
Klippel-Trenaunay Syndrome Patient Stories | Boston Childrens HospitalKlippel-Trenaunay Syndrome Patient Stories | Boston Childrens Hospital
Read about the journeys of our patients with Klippel-Trenaunay Syndrome from experts at Boston Childrens, ranked best Childrens Hospital by US News.
http://www.childrenshospital.org/conditions-and-treatments/conditions/k/klippel-trenaunay-syndrome/patient-stories
6.3.5 Headache attributed to encephalotrigeminal or leptomeningeal angiomatosis (Sturge Weber syndrome) - ICHD-36.3.5 Headache attributed to encephalotrigeminal or leptomeningeal angiomatosis (Sturge Weber syndrome) - ICHD-3
Angiomatosis, Familial Cerebelloretinal - Medical Dictionary online-medical-dictionary.orgAngiomatosis, Familial Cerebelloretinal - Medical Dictionary online-medical-dictionary.org
An autosomal dominant disorder caused by Mutations in a Tumor Suppressor Gene. This Syndrome is characterized by abnormal Growth of small Blood Vessels leading to a host of Neoplasms. They include Hemangioblastoma in the Retina; Cerebellum; and SPINAL CORD; Pheochromocytoma; pancreatic Tumors; and Renal Cell Carcinoma (see Carcinoma, Renal Cell). Common clinical signs include Hypertension and neurological dysfunctions ...
http://www.online-medical-dictionary.org/definitions-a/angiomatosis-familial-cerebelloretinal.html
Klippel-Trenaunay Syndrome (vascular malformation-deregulated growth syndrome[s], VM-DG type 3/Girth type/Klippel-Trenaunay...Klippel-Trenaunay Syndrome (vascular malformation-deregulated growth syndrome[s], VM-DG type 3/Girth type/Klippel-Trenaunay...
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http://www.oncologynurseadvisor.com/dermatology/klippel-trenaunay-syndrome-vascular-malformation-deregulated-growth-syndromes-vm-dg-type-3girth-typeklippel-trenaunay-type-kts-klipppel-trenaunay-weber-and-angioosteohypertrophy-syndrome/article/588773/
Phaeochromocytoma and cerebellar haemangioblastoma. | Journal of Neurology, Neurosurgery & PsychiatryPhaeochromocytoma and cerebellar haemangioblastoma. | Journal of Neurology, Neurosurgery & Psychiatry
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Centers RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.. ...
https://jnnp.bmj.com/content/30/5/443
Long-term results of intravitreal ranibizumab for the treatment of retinal angiomatous proliferation and utility of an advanced...Long-term results of intravitreal ranibizumab for the treatment of retinal angiomatous proliferation and utility of an advanced...
Methods We retrospectively reviewed 17 treatment-naïve eyes in 14 patients (4 men, 10 women; age range 71-87 years; mean age 80 years) treated with IVR. All the patients received three consecutive monthly injections of 0.5 mg/0.05 mL of ranibizumab as an induction treatment. Retreatment was allowed if evidence of clinical deterioration was noted or if an SD-OCT examination performed at a 1-month follow-up showed intraretinal oedema, subretinal fluid, or recurrent pigment epithelial detachment. The primary outcome measures were best-corrected visual acuity (BCVA) and central foveal thickness (CFT) as evaluated using SD-OCT. Furthermore, we investigated the atrophic area at 36 months using advanced RPE analysis provided by SD-OCT and analysed the correlation with the BCVA.. ...
http://bjo.bmj.com/content/early/2014/03/05/bjophthalmol-2013-304251
Ranibizumab in monotherapy and combined with photodynamic therapy for | OPTHRanibizumab in monotherapy and combined with photodynamic therapy for | OPTH
Ranibizumab in monotherapy and combined with photodynamic therapy for retinal angiomatous proliferation Luis Arias,1–3 Francisco Gómez-Ulla,2–4 José M Ruiz-Moreno2,3,51Ophthalmology Department, Bellvitge University Hospital, C/Feixa Llarga, L’Hospitalet de Llobregat, Barcelona, 2Spanish Vitreoretinal Society (SERV), C/Xosé Chao Rego, Santiago de Compostela, 3RETICS OFTARED, Institute of Health Carlos III, C/Sinesio Delgado, Madrid, 4Gómez-Ulla Eye Institute, Santiago de Compostela, 5Department of Ophthalmology, Albacete University Hospital, Avenida de Almansa s/n, Albacete, Spain Purpose: To compare the effects of intravitreal ranibizumab in monotherapy (group A) and combined with photodynamic therapy (PDT) with verteporfin (group B) in retinal angiomatous proliferation (RAP) treatment.Methods: This was a multicentric, prospective, randomized clinical study conducted with parallel groups. The study eye in both groups received ranibizumab on days 1, 30, and
https://www.dovepress.com/ranibizumab-in-monotherapy-and-combined-with-photodynamic-therapy-for--peer-reviewed-article-OPTH
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Article - Klippel-Trenaunay syndromeArticle - Klippel-Trenaunay syndrome
CASE SUMMARY A 5-month-old girl presented with recurrent seizures. The child was born at 36 weeks via C-section due to prenatal ultrasound abnormalities of t...
https://www.appliedradiology.com/articles/klippel-trenaunay-syndrome
Von Hippel Lindau Syndrome | Syndromes: Rapid Recognition and Perioperative Implications | AccessAnesthesiology | McGraw-Hill...Von Hippel Lindau Syndrome | Syndromes: Rapid Recognition and Perioperative Implications | AccessAnesthesiology | McGraw-Hill...
The estimated birth incidence in East Anglia, Norfolk, UK, is believed to be 1:36,000 live births and an estimated prevalence of heterozygotes to be 1 in 53,000. Direct and indirect estimates of the mutation rate were 4.4 per million gametes per generation and 2.32 per million gametes per generation, respectively. There are no significant associations between parental age or birth order and new mutations. In the Freiburg district of Germany, the prevalence has been calculated for this disorder to be 1 in 38,951. In the northwest of England, 83 affected persons were reported in 1996 and the calculated prevalence for this disease was estimated (heterozygotes) in the region to be 1 in 85,000 persons, with an estimated birth incidence of 1 in 45,500 live births. The incidence of the most common lesions are as follows: retinal angiomatosis (57%), cerebellar (55%), medullary (6%), and spinal (14%) hemangioblastomas; pheochromocytoma (19%), renal cysts (14%), renal cell carcinoma (24%), epididymal ...
https://accessanesthesiology.mhmedical.com/content.aspx?bookid=852§ionid=49518315
Syndrome Archives
Glaucoma or high pressure around the eyes is one of the conditions that are apparent at birth time or show up later. The occurrence of the glaucoma in persons with the Encephalotrigeminal Angiomatosis is said to be about 40% and 70% in choroidal lesions. Glaucoma is normally limited to the eye covered by the stain. Also eye enlargement (buphthalmos) is also a common occurrence for the stain affected eye. Numerous other bodily organs are less affected by the condition.. Treatment. Treatment by way of laser is employed to get rid of and/or lighten the birthmarks for children as little as a month old. By use of anti-convulsants, seizures can easily be controlled. Also a brain surgery as well as VNS implants can be employed to assist in seizure management. Oral medications or eye drops can be used to help manage glaucoma. Should all the oral and topical administered medications fail to be effective, then the only other option would certainly be surgery.. ...
http://lets-jam.com/category/syndrome/
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症例報告 出生時に下肢の血管腫を認め経過観察中に静脈瘤,片側肥大が出現し診断に至ったKlippel-Trenaunay-Weber症候群の1例 （2018 ...
https://ci.nii.ac.jp/author?q=%E7%99%BD%E4%BA%95+%E5%8B%9D
Lasers for Telangiectasias NY | Facial Telangiectasias TreatmentsLasers for Telangiectasias NY | Facial Telangiectasias Treatments
Telangiectasias, also known as spider veins, can be effectively addressed with laser treatments. Contact Gendler Dermatology for a laser consultation.
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VHL QuickView - Correlation Engine
Von Hippel-Lindau syndrome (VHL) is a dominantly inherited familial cancer syndrome predisposing to a variety of malignant and benign tumors. A germline mutation of this gene is the basis of familial inheritance of VHL syndrome. The protein encoded by thi…
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According to reviews about an English show about air in Australia on iTV called Brief Encounters, the 80s delivered a second sexual revolution for the Brits with the rise of the Ann Summers party plan business. So, its now the noughties, is Australia finally ready for the revolution?. One UK review quoted: With an Ann Summers store on pretty much every British high-street, its strange to think back to a time when the stores sex toys and exotic lingerie were utterly taboo. I read this and it struck me - its 30 years on and really, it still is largely taboo in Australia!. PASH Australia was launched over 10 years ago now with a goal to help the women of Australia have access to information and sensuality products that would enhance relationships, encourage intimacy and build female sexual self-confidence. My goal was to remove the stigma and empower women. I wanted to create something that would appeal to all women - hence the absence of exotic lingerie and smutty toys!. I have to ...
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https://commons.wikimedia.org/wiki/Category:Sant_Ramon
What are Telangiectasias | Empire Medical TrainingWhat are Telangiectasias | Empire Medical Training
Telangiectasias (aka spider veins, varicose veins, thread veins) are blood vessels typically less than 2mm in diameter and can be either blue (de-oxy) or red (oxy) in color.
https://www.empiremedicaltraining.com/resources/telangiectasias/
Supplementary MaterialsAdditional document 1: Amount S1: Working super model tiffany livingston - bcl-2 family members and the...Supplementary MaterialsAdditional document 1: Amount S1: Working super model tiffany livingston - bcl-2 family members and the...
Supplementary MaterialsAdditional document 1: Amount S1: Working super model tiffany livingston for polar overdominance on the ovine callipyge locus [11]. noticed mutation off their sire (genotype?pets. This ectopic appearance outcomes from the inactivation C with the A to G stage mutation C of the muscle-specific silencer component that post-natally downregulates the appearance of and in pets do not exhibit the Saracatinib supplier phenotype because and genes are imprinted in support of expressed in the paternal allele. It really is thought that pets do not exhibit the phenotype due Saracatinib supplier to the excess ectopic appearance of non-coding RNAs (ncRNAs) that are (i) imprinted and portrayed in the maternal allele, (ii) managed in with the same muscle-specific silencer component, and (iii) post-transcriptionally down-regulating and in locus consist of four lengthy ncRNAs (lncRNA) (as well as the transcripts by at least three properly complementary miRNAs prepared in the maternally ...
http://www.informationalwebs.com/2019/06/25/supplementary-materialsadditional-document-1-amount-s1-working-super-model-tiffany-livingston/
ATR inhibitors VE-821 and VX-970 sensitize cancer cells to topoisomerase I inhibitorsATR inhibitors VE-821 and VX-970 sensitize cancer cells to topoisomerase I inhibitors
Supplementary MaterialsS1 Data: Summarised beliefs result from simulations utilized to create heatmaps in Figs ?Figs1,1, ?,3,3, ?,4,4, ?,5,5, ?,7,7, ?,10,10, S13 and S1CS3. to 0.4. Organic data are tabulated in S1 Data.(PDF) pbio.1002394.s002.pdf (501K) GUID:?8A277BD2-6F01-4DC3-94AE-4B3534D4E29B S2 Fig: Ramifications of the frequency and amplitude of cell population oscillations in MGE transmitting. (A) This heatmap summarises simulations Anamorelin HCl where the amplitude (gene, necessary for efficient change, is certainly unchanged. (B) Annotation from the guide genome of Taiwan19F-14. Portable hereditary element-related sequences (the Tnand disruption could be from the insertion of the prophage in to the gene.(PDF) pbio.1002394.s006.pdf (2.4M) GUID:?581C7D54-0373-4CFE-B1C3-9046CEFED6E8 S6 Fig: Apparent removal of an MGE via an interstrain transformation event. (A) Optimum possibility phylogeny of BC14 reps isolated from longitudinally sampled hosts predicated on stage mutations beyond ...
http://icrs-world-congress.org
Mitochondria from diverse organisms can handle transporting huge amounts of Ca2+ - Drug Resistance to EGFR Inhibitors in Lung...Mitochondria from diverse organisms can handle transporting huge amounts of Ca2+ - Drug Resistance to EGFR Inhibitors in Lung...
Mitochondria from diverse organisms can handle transporting huge amounts of Ca2+ with a ruthenium-red-sensitive membrane-potential-dependent system called the uniporter1-4. potential remain intact fully. MCU provides two forecasted transmembrane helices that are separated by an extremely conserved linker facing the intermembrane space. Acidic residues within this linker are necessary for its complete activity. Nevertheless an S259A stage mutation retains function but confers level of resistance to Ru360 the strongest inhibitor from the uniporter. Our genomic physiological pharmacological and biochemical data LY341495 firmly establish MCU as an important element of the mitochondrial Ca2+ uniporter. To anticipate proteins that are functionally linked to MICU1 (ref. 5) and needed for mitochondrial calcium mineral (Ca2+) uptake we performed three organized computational analyses. First we positioned all ~20 0 mammalian genes based on the similarity of their phylogenetic profile to across 81 mouse ...
http://elevateblogconference.com/mitochondria-from-diverse-organisms-can-handle-transporting-huge-amounts-of-ca2/
Adoptive transfer of T cells genetically improved to sole anti-TSLPR chimeric | Resveratrol downregulates PI3K/Akt/mTOR...Adoptive transfer of T cells genetically improved to sole anti-TSLPR chimeric | Resveratrol downregulates PI3K/Akt/mTOR...
Adoptive transfer of T cells genetically improved to sole anti-TSLPR chimeric antigen receptors can cure B-ALL in xenograft kinds. Philadelphia chromosomeClike (Ph-like) leukemias react badly to regular chemotherapy RICTOR and possess Angiotensin III (human, mouse) high prices of relapse.17 Multiple groupings have got Angiotensin III (human, mouse) now demonstrated that rearrangements accounts for fifty percent of Ph-like ALL genomic alterations and are also highly associated with concomitant and stage mutations.17,18,20,21,32 We keep that the TSLPR features as an ALL oncoprotein provided its cell surface area reflection and association with poor scientific outcomes and thus might be an ideal immunotherapeutic focus on. Furthermore, TSLPR phrase in regular tissue shows up to end up being limited. We demonstrate that a TSLPR CAR may eradicate individual Web site Angiotensin III (human, mouse) completely. For structure of the lengthy CAR constructs, the CH2CH3 websites from IGHG1 ...
http://87paydays.info/adoptive-transfer-of-t-cells-genetically-improved-to-sole-anti-tslpr-chimeric/
Rabbit polyclonal to PAX2 | Safety, pharmacokinetics, and pharmacodynamic properties of oral DEBIO1143 (AT-406)Rabbit polyclonal to PAX2 | Safety, pharmacokinetics, and pharmacodynamic properties of oral DEBIO1143 (AT-406)
Background Accurate prediction of peptide immunogenicity and characterization of relation between peptide sequences and peptide immunogenicity will be greatly helpful for vaccine designs and understanding of the immune system. immunogenicity data from three major immunology databases. In order to consider the effect of MHC restriction, peptides are classified by their associated MHC alleles. Subsequently, a computational method (called POPISK) using support vector machine using a weighted level string kernel is certainly proposed to anticipate T-cell reactivity and recognize essential reputation positions. POPISK produces a mean 10-fold cross-validation precision of 68% in predicting T-cell reactivity of HLA-A2-binding peptides. POPISK is certainly with the capacity of predicting immunogenicity with ratings that may also correctly anticipate the modification in T-cell reactivity linked to stage mutations in epitopes reported in prior research using crystal buildings. Thorough analyses from the ...
http://at-406.net/tag/rabbit-polyclonal-to-pax2/
Cutaneous vascular proliferation. Part II. Hyperplasias and benign neoplasms.Cutaneous vascular proliferation. Part II. Hyperplasias and benign neoplasms.
This second part of our review about vascular proliferations summarizes the clinicopathologic features of the cutaneous vascular hyperplasias and benign neoplasms. Hyperplasias com..
https://www.omicsonline.org/references/cutaneous-vascular-proliferation-part-ii-hyperplasias-and-benign-neoplasms-95650.html
The Sturge-Weber Foundation : New to SWF : Understanding Sturge-WeberThe Sturge-Weber Foundation : New to SWF : Understanding Sturge-Weber
How Do We Use Information Collected From Cookies? We use website browser software tools such as cookies and web server logs to gather information about our website users browsing activities, in order to constantly improve our website and better serve our users. This information assists us to design and arrange our web pages in the most user-friendly manner and to continually improve our website to better meet the needs of our users and prospective users. Cookies help us collect important business and technical statistics. The information in the cookies lets us trace the paths followed by users to our website as they move from one page to another. Web server logs allow us to count how many people visit our website and evaluate our websites visitor capacity. We do not use these technologies to capture your individual email address or any personally identifying information about you ...
http://sturge-weber.org/new-to-swf/
Most recent papers with the keyword klippel -trenaunay | Read by QxMDMost recent papers with the keyword klippel -trenaunay | Read by QxMD
Neural tube defects are congenital development anomaly of the central nervous system and usually have relatively more predilection to affect at anterior and posterior neuropore embryological development sites, so usually one or two defects are commonly encountered. However, occurrence of simultaneous multiple neural tube defects is very rare, presence of constellation of five neural defects is extremely rare, and all defects add up together to produce gross neurological deficit. We present an interesting case of a 23-year-old male who presented with history of lower backache and noticed wasting and weakness of lower limbs associated with difficulty in walking for the last 2 years but had no associated sphincter disturbances ...
https://www.readbyqxmd.com/keyword/97759
A Phase III, Randomized, Double-Blind, Placebo-Controlled Trial of Pegfilgrastim in Patients Receiving First-Line FOLFOX...A Phase III, Randomized, Double-Blind, Placebo-Controlled Trial of Pegfilgrastim in Patients Receiving First-Line FOLFOX...
Authors: Tamas Pinter, Zandra Klippel, Alvydas Cesas, Adina Croitoru, Jochen Decaestecker, Peter Gibbs, Yevhen Hotko, Jacek Jassem, Galina Kurteva, Jan Novotny, Seamus OReilly, Tomas Salek, Maureen Reiner, Phuong Khanh Morrow, Mi Rim Choi, Sadie Whittaker, Charles Blanke
https://findanexpert.unimelb.edu.au/scholarlywork/1186895-a-phase-iii--randomized--double-blind--placebo-controlled-trial-of-pegfilgrastim-in-patients-receiving-first-line-folfox-bevacizumab-or-folfiri-bevacizumab-for-locally-advanced-or-metastatic-colorectal-cancer--final-results-of-the-pegfilgrastim-and-anti-vegf-evaluation-study-
Pa empresa<...Pa empresa<...
ADC ta kla pa yuda hasi i mantené e kalidat di e produkto- i servisionan di empresanan optimal. Esaki ta konta pa e integridat di e empresa su trahadónan tambe. Al fin al kabo: bon produkto i servisio - i tambe e salú di trahadó - ta aspektonan esensial pa kada empresa.. ADC ta hasi tèstnan di laboratorio ku ta moderno, presis i na e nivel di mas haltu. Esaki ta yuda médikonan lokal pa ta dirigí i lihé ku nan diagnósis. E tratamentunan di mas mihó ta bira posibel e ora ei pa e pashèntnan.. Pero e ekspertisio di ADC por ta hopi balioso pa e salú di empresanan tambe. Análisisnan spesialista, hasí for di diferente disiplina, ta duna informashon relevante i konfiabel ku kua por mantené e kalidat di produkshon i di servisio na nivel, a base di datonan real.. ...
https://www.adcnv.com/servisionan/pa-empresa/
CONGRES-MEDICAL: Equipement m dical : Prochains Ev nements, congres, conf rences, formations m dicales en medecine et sant :...CONGRES-MEDICAL: Equipement m dical : Prochains Ev nements, congres, conf rences, formations m dicales en medecine et sant :...
Equipement m dical - Prochains Ev nements, congres, conf rences, formations m dicales en medecine et sant - Site de r f rencement et promotions de congres, v nement m dicaux et param dicaux mondiaux
http://congres-medical.com/modules.php?pageNum_plancap_peche=0&totalRows_plancap_peche=7&name=3c01_Event&filter=&type=&letter=&id_sousrub=18&op=secteur
Formet av fortidenFormet av fortiden
Det sies en god barndom varer livet ut, og det er mye sant i de ordene. Det som også er sant, er at en tøff barndom kan ha langvarige konsekvenser. Økt risiko for psykisk og fysisk sykdom, lavere forventet levealder og generelt dårligere livskvalitet1⁠, for å nevne noe. Selv om man er blitt voksen og…
https://sinnsstemninger.wordpress.com/2016/04/03/formet-av-fortiden/
AngiomatosisAngiomatosis
... is a non-neoplastic condition characterised by nests of proliferating capillaries arranged in a lobular pattern, ... "angiomatosis" at Dorland's Medical Dictionary "Von Hippel-Lindau Disease (VHL) Information Page". www.ninds.nih.gov. National ... Bacillary angiomatosis Klippel-Trénaunay syndrome Sturge-Weber syndrome It is a vascular malformation wherein blood vessels ... Prognosis depends on the size and location of the tumour, untreated angiomatosis may lead to blindness and/ or permanent brain ...
https://en.wikipedia.org/wiki/Angiomatosis
Universal angiomatosisUniversal angiomatosis
... (also known as "Generalized telangiectasia") is a bleeding disease that affects the blood vessels of the ...
https://en.wikipedia.org/wiki/Universal_angiomatosis
Bacillary angiomatosisBacillary angiomatosis
... the term bacillary angiomatosis was widely adopted. Cat scratch fever Trench fever Angiomatosis "Bacillary Angiomatosis: ... Bacillary angiomatosis (BA) is a form of angiomatosis associated with bacteria of the genus Bartonella. Cutaneous BA is ... Mateen FJ, Newstead JC, McClean KL (July 2005). "Bacillary angiomatosis in an HIV-positive man with multiple risk factors: A ... Gasquet S, Maurin M, Brouqui P, Lepidi H, Raoult D (1998). "Bacillary angiomatosis in immunocompromised patients". AIDS. 12 (14 ...
https://en.wikipedia.org/wiki/Bacillary_angiomatosis
Arvid LindauArvid Lindau
Angiomatosis retinae. Acta pathologica et microbiologica Scandinavica, Copenhagen, 1926, supplement 1: 77. Von Hippel-Lindau ... Bau, Pathogenese und Beziehungen zur Angiomatosis retinae, (doctoral thesis); Acta pathologica et microbiologica Scandinavica, ... "angiomatosis of the central nervous system". This disease is characterized by tumors of the retina and the brain, along with ...
https://en.wikipedia.org/wiki/Arvid_Lindau
Bannayan-Riley-Ruvalcaba syndromeBannayan-Riley-Ruvalcaba syndrome
ISBN 978-1-84619-099-5. Bannayan, G. A. (1 July 1971). "Lipomatosis, angiomatosis, and macrencephalia. A previously undescribed ...
https://en.wikipedia.org/wiki/Bannayan–Riley–Ruvalcaba_syndrome
Stanley FalkowStanley Falkow
"The agent of bacillary angiomatosis. An approach to the identification of uncultured pathogens". The New England Journal of ...
https://en.wikipedia.org/wiki/Stanley_Falkow
Von Hippel-Lindau diseaseVon Hippel-Lindau disease
Other uncommon names are: angiomatosis retinae, familial cerebello-retinal angiomatosis, cerebelloretinal hemangioblastomatosis ... Lindau A (1927). "Zur Frage der Angiomatosis Retinae und Ihrer Hirncomplikation". Acta Ophthalmol. 4 (1-2): 193-226. doi: ... February 2007). "Genotype-phenotype correlation in von Hippel-Lindau disease with retinal angiomatosis". Archives of ... Conditions associated with VHL disease include angiomatosis, hemangioblastomas, pheochromocytoma, renal cell carcinoma, ...
https://en.wikipedia.org/wiki/Von_Hippel–Lindau_disease
Emerich UllmannEmerich Ullmann
Ullmann's syndrome: A systemic angiomatosis due to multiple arteriovenous malformations. NCBI Emerich Ullmann and Organ ...
https://en.wikipedia.org/wiki/Emerich_Ullmann
Peliosis hepatisPeliosis hepatis
"Molecular epidemiology of bartonella infections in patients with bacillary angiomatosis-peliosis". N. Engl. J. Med. 337 (26): ...
https://en.wikipedia.org/wiki/Peliosis_hepatis
Cancer syndromeCancer syndrome
February 2007). "Genotype-phenotype correlation in von Hippel-Lindau disease with retinal angiomatosis". Archives of ...
https://en.wikipedia.org/wiki/Cancer_syndrome
Bartonella quintanaBartonella quintana
B. quintana also induces lesions seen in bacillary angiomatosis that protrude into vascular lumina, often occluding blood flow ... In trench fever or B. quintana-induced endocarditis patients, bacillary angiomatosis lesions are also seen. Notably, ... "Bacillary Angiomatosis: The Histopathology and Differential Diagnosis of a Pseudoneoplastic Infection in Patients with Human ... "Molecular Epidemiology of Bartonella Infections in Patients with Bacillary Angiomatosis-Peliosis". New England Journal of ...
https://en.wikipedia.org/wiki/Bartonella_quintana
Bacillary peliosisBacillary peliosis
December 1997). "Molecular epidemiology of bartonella infections in patients with bacillary angiomatosis-peliosis". N. Engl. J ...
https://en.wikipedia.org/wiki/Bacillary_peliosis
PhakomatosisPhakomatosis
"Retinal angiomatosis in von Hippel-Lindau disease: a longitudinal ophthalmologic study". Ophthalmology. 113 (8): 1418-1424. doi ...
https://en.wikipedia.org/wiki/Phakomatosis
Sturge-Weber syndromeSturge-Weber syndrome
... , sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin ... Imaging findings may include tram track calcifications on CT, pial angiomatosis, and hemicerebral atrophy. Sturge-Weber ... imaging should be performed to screen for intracranial leptomeningeal angiomatosis. The haemangioma present on the surface of ...
https://en.wikipedia.org/wiki/Sturge–Weber_syndrome
TauopathyTauopathy
Halper J, Scheithauer BW, Okazaki H, Laws ER (July 1986). "Meningio-angiomatosis: a report of six cases with special reference ...
https://en.wikipedia.org/wiki/Tauopathy
Neurofibrillary tangleNeurofibrillary tangle
Halper, J; Scheithauer, BW; Okazaki, H; Laws Jr, ER (1986). "Meningio-angiomatosis: a report of six cases with special ...
https://en.wikipedia.org/wiki/Neurofibrillary_tangle
Developmental venous anomalyDevelopmental venous anomaly
DVA can also be found diagnosed with Sturge-Weber syndrome and can be found through leptomeningeal angiomatosis. Demyelinating ...
https://en.wikipedia.org/wiki/Developmental_venous_anomaly
Trench feverTrench fever
Bartonella quintana is closely related to Bartonella henselae, the agent of cat scratch fever and bacillary angiomatosis. The ...
https://en.wikipedia.org/wiki/Trench_fever
Alternating hemiplegiaAlternating hemiplegia
If a port-wine stain around the eye is found, the patient should be screened for intracranial leptomeningeal angiomatosis. ...
https://en.wikipedia.org/wiki/Alternating_hemiplegia
BartonellosisBartonellosis
Peliosis hepatis can be associated with peliosis of the spleen, as well as bacillary angiomatosis of the skin in HIV patients. ... B. henselae can be associated with bacteremia, bacillary angiomatosis, and peliosis hepatis in HIV patients, and bacteremia and ... Kemper CA, Lombard CM, Deresinski SC, Tompkins LS (August 1990). "Visceral bacillary epithelioid angiomatosis: possible ... and bacillary angiomatosis. Pathological response can vary with the immune status of the host. Infection with B. henselae can ...
https://en.wikipedia.org/wiki/Bartonellosis
William A. PetriWilliam A. Petri
Journal of Clinical Investigation 80:1238-1244, 1987 doi:10.1172/JCI113198 Cat-Scratch Disease, Bacillary Angiomatosis, and ...
https://en.wikipedia.org/wiki/William_A._Petri
Cat-scratch diseaseCat-scratch disease
... such as bacillary angiomatosis or bacillary peliosis. Bacillary angiomatosis is primarily a vascular skin lesion that may ...
https://en.wikipedia.org/wiki/Cat-scratch_disease
Hereditary neurocutaneous angiomaHereditary neurocutaneous angioma
Leblanc, Richard (2004), Roach, E. Steve; Miller, Van S. (eds.), "Hereditary neurocutaneous angiomatosis", Neurocutaneous ... from paraplegia as a result of an intraspinal AV malformation which was the consequence of cutaneomeningospinal angiomatosis. ...
https://en.wikipedia.org/wiki/Hereditary_neurocutaneous_angioma
Kaposis sarcomaKaposi's sarcoma
Histiocytoma Cryptococcosis Histoplasmosis Leishmaniasis Pneumocystis lesions Dermatophytosis Angioma Bacillary angiomatosis ...
https://en.wikipedia.org/wiki/Kaposi's_sarcoma
Eugen von HippelEugen von Hippel
... "angiomatosis retinae". However it wasn't until 1926 that Swedish pathologist Arvid Lindau recognized an association between ... angiomatosis of the retina with hemangioblastomas of the cerebellum and other parts of the central nervous system. This ...
https://en.wikipedia.org/wiki/Eugen_von_Hippel
Angelo MaffucciAngelo Maffucci
... the skeletal angiomatosis. Maffucci continued his anatomical and experimental studies on liver pathology, making the important ...
https://en.wikipedia.org/wiki/Angelo_Maffucci
Gorhams diseaseGorham's disease
2010 Mar;46(3):873-6. Aviv RI, McHugh K, Hunt J. Angiomatosis of bone and soft tissue: a spectrum of disease from diffuse ... However it is accomplished, the progressive osteolysis is always associated with an angiomatosis of blood and sometimes of ... that advanced the hypothesis that angiomatosis was responsible for this unusual form of massive osteolysis. That same year, ... anomalies always occupied space that normally would be filled with new bone and speculated that the presence of angiomatosis ...
https://en.wikipedia.org/wiki/Gorham's_disease
BH11960BH11960
... such as bacillary angiomatosis, peliosis hepatis, endocarditis, and bacteremia (22). Even in cases of severe disease, ...
https://en.wikipedia.org/wiki/BH11960
List of diseases (C)List of diseases (C)
... syndrome Cystathionine beta synthetase deficiency Cystic adenomatoid malformation of lung Cystic angiomatosis of bone, diffuse ... Capillary leak syndrome Capillary leak syndrome with monoclonal gammopathy Capillary venous leptomeningeal angiomatosis ...
https://en.wikipedia.org/wiki/List_of_diseases_(C)
Trimeric autotransporter adhesinTrimeric autotransporter adhesin
... it is more serious as it can lead to bacillary angiomatosis. This a condition where benign tumours of the blood vessels undergo ...
https://en.wikipedia.org/wiki/Trimeric_autotransporter_adhesin
Bacillary Angiomatosis: Practice Essentials, Background, PathophysiologyBacillary Angiomatosis: Practice Essentials, Background, Pathophysiology
Bacillary angiomatosis is a vascular, proliferative form of Bartonella infection that occurs primarily in immunocompromised ... 9, 10, 11, 12] Initially, bacillary angiomatosis was called epithelioid angiomatosis, because of its histologic appearance. ( ... encoded search term (Bacillary Angiomatosis) and Bacillary Angiomatosis What to Read Next on Medscape ... has also been detected in and cultured from lesions caused by bacillary angiomatosis. Bacillary angiomatosis due to Bartonella ...
https://www.medscape.com/answers/212737-173018/how-is-bacillary-angiomatosis-treated
Unraveling Mysteries Associated with Cat-Scratch Disease, Bacillary Angiomatosis, and Related Syndromes - Volume 1, Number 1...
Tappero JW, Koehler JE, Berger TG, Cockerell CJ, Lee T-H, Busch MP, Bacillary angiomatosis and bacillary splenitis in ... Tappero JW, Mohle-Boetani J, Koehler JE, Swaminathan B, Berger TG, LeBoit PE, The epidemiology of bacillary angiomatosis and ... Cat scratch disease, bacillary angiomatosis, and other infections due to Rochalimaea. N Engl J Med. 1994;330:1509-15. DOIPubMed ... Cat scratch disease and bacillary angiomatosis [letter]. JAMA. 1991;266:1938-9. DOIPubMedGoogle Scholar ...
http://wwwnc.cdc.gov/eid/article/1/1/09-0103_article.htm
Meningo-cortical calcifying angiomatosis and celiac disease<...
Meningo-cortical calcifying angiomatosis and celiac disease. L. La Mantia, B. Pollo, M. Savoiardo, A. Costa, M. Eoli, A. ... Meningo-cortical calcifying angiomatosis and celiac disease. / La Mantia, L.; Pollo, B.; Savoiardo, M. et al. ... Meningo-cortical calcifying angiomatosis and celiac disease. Clinical Neurology and Neurosurgery. 1998 Sep;100(3):209-215. ... Meningo-cortical calcifying angiomatosis and celiac disease. In: Clinical Neurology and Neurosurgery. 1998 ; Vol. 100, No. 3. ...
https://moh-it.pure.elsevier.com/en/publications/meningo-cortical-calcifying-angiomatosis-and-celiac-disease
Is body wraps and electrical treatments contraindicated for bacillary angiomatosis?Is body wraps and electrical treatments contraindicated for bacillary angiomatosis?
Bacillary angiomatosis is a vascular, proliferative form of Bartonella infection that occurs primarily in immunocompromised ... Bacillary angiomatosis is the second-most-common cause of angiomatous skin lesions in persons infected with the human ... Bacillary angiomatosis is a vascular, proliferative form of Bartonella infection that occurs primarily in immunocompromised ...
https://www.salon-compass.com/contraindications/is-body-wraps-and-electrical-treatments-contraindicated-for-bacillary-angiomatosis/
IMSEAR at SEARO: Incomplete monosymptomatic leptomeningeal angiomatosis.
Incomplete monosymptomatic leptomeningeal angiomatosis.. Autor : Kumar, Sarita. Muranjan, Mamta N. Tullu, Milind S. Lahiri, ... Incomplete monosymptomatic leptomeningeal angiomatosis. Indian Journal of Pediatrics. 2004 Oct; 71(10): 947. ... Our case qualifies to be called incomplete monosymptomatic leptomeningeal angiomatosis.. URI : http://imsear.searo.who.int/ ...
https://imsear.searo.who.int/handle/123456789/79613?locale=es
How to treat bacillary angiomatosis? - Sage-AdvicesHow to treat bacillary angiomatosis? - Sage-Advices
How do you get bacillary angiomatosis?. Bacillary angiomatosis (epithelioid angiomatosis) is an uncommon disease characterized ... What causes bacillary angiomatosis?. Bacillary angiomatosis is skin infection caused by the gram-negative bacteria Bartonella ... What is Angiomatosis?. Angiomatosis is a diffuse vascular lesion which clinically mimics hemangioma or vascular malformation. ... What is Leptomeningeal Angiomatosis?. Leptomeningeal angiomatosis is a congenital vascular anomaly characterized by venous ...
https://sage-advices.com/how-to-treat-bacillary-angiomatosis/
1993 Revised Classification System for HIV Infection and Expanded Surveillance Case Definition for AIDS Among Adolescents and...1993 Revised Classification System for HIV Infection and Expanded Surveillance Case Definition for AIDS Among Adolescents and...
Bacillary angiomatosis *. Candidiasis, oropharyngeal (thrush) *. Candidiasis, vulvovaginal; persistent, frequent, or poorly ...
https://www.cdc.gov/MMWR/preview/mmwrhtml/00018871.htm
Sturge-Weber syndrome: MedlinePlus Medical EncyclopediaSturge-Weber syndrome: MedlinePlus Medical Encyclopedia
Sturge-Weber syndrome (SWS) is a rare disorder that is present at birth. A child with this condition will have a port-wine stain birthmark (usually on the face) and may have nervous system problems.
https://medlineplus.gov/ency/article/001426.htm
List of parasites of humans - WikipediaList of parasites of humans - Wikipedia
Toxoplasmosis is becoming a global health hazard as it infects 30-50% of the world human population. Clinically, the life-long presence of the parasite in tissues of a majority of infected individuals is usually considered asymptomatic. However, a number of studies show that this asymptomatic infection may also lead to development of other human pathologies. ... The seroprevalence of toxoplasmosis correlated with various disease burden. Statistical associations does not necessarily mean causality. The precautionary principle suggests however that possible role of toxoplasmosis as a triggering factor responsible for development of several clinical entities deserves much more attention and financial support both in everyday medical practice and future clinical research ...
https://en.wikipedia.org/wiki/List_of_parasites_of_humans
Bacillary angiomatosis and related diseases caused by Rochalimaea<...
Bacillary angiomatosis and related diseases caused by Rochalimaea. / Cockerell, C. J.. In: Journal of the American Academy of ... Bacillary angiomatosis and related diseases caused by Rochalimaea. Journal of the American Academy of Dermatology. 1995 May;32( ... Cockerell, C. J. / Bacillary angiomatosis and related diseases caused by Rochalimaea. In: Journal of the American Academy of ... Cockerell, C. J. (1995). Bacillary angiomatosis and related diseases caused by Rochalimaea. Journal of the American Academy of ...
https://utsouthwestern.pure.elsevier.com/en/publications/bacillary-angiomatosis-and-related-diseases-caused-by-rochalimaea
Unraveling Mysteries Associated with Cat-Scratch Disease, Bacillary Angiomatosis, and Related Syndromes - Volume 1, Number 1...
Tappero JW, Koehler JE, Berger TG, Cockerell CJ, Lee T-H, Busch MP, Bacillary angiomatosis and bacillary splenitis in ... Tappero JW, Mohle-Boetani J, Koehler JE, Swaminathan B, Berger TG, LeBoit PE, The epidemiology of bacillary angiomatosis and ... Cat scratch disease, bacillary angiomatosis, and other infections due to Rochalimaea. N Engl J Med. 1994;330:1509-15. DOIPubMed ... Cat scratch disease and bacillary angiomatosis [letter]. JAMA. 1991;266:1938-9. DOIPubMedGoogle Scholar ...
https://wwwnc-origin.cdc.gov/eid/article/1/1/09-0103
Diffuse dermal angiomatosis: a rare cause of painful ulceration in renal insufficiency. | Clin Exp Dermatol;47(6): 1182-1183,...Diffuse dermal angiomatosis: a rare cause of painful ulceration in renal insufficiency. | Clin Exp Dermatol;47(6): 1182-1183,...
Diffuse dermal angiomatosis is a rare, benign, reactive cutaneous vascular proliferation that has been reported in the context ... Diffuse dermal angiomatosis: a rare cause of painful ulceration in renal insufficiency. ... Diffuse dermal angiomatosis: a rare cause of painful ulceration in renal insufficiency. ...
https://pesquisa.bvsalud.org/controlecancer/resource/pt/mdl-35014721
Cardiology - Janeway Tower | Atrium Health Wake Forest BaptistCardiology - Janeway Tower | Atrium Health Wake Forest Baptist
Find a cardiology clinic near you at Cardiology - Janeway Tower, offering personalized cardiology treatments and heart care in Winston-Salem, NC.
https://www.wakehealth.edu/locations/clinics/c/cardiology-janeway-tower-7th-floor
1993 Revised Classification System for HIV Infection and Expanded Su1993 Revised Classification System for HIV Infection and Expanded Su
Bacillary angiomatosis *Candidiasis, oropharyngeal (thrush) *Candidiasis, vulvovaginal; persistent, frequent, or poorly ...
https://wonder.cdc.gov/wonder/prevguid/m0018871/m0018871.asp
Search Results: Ankle - skin of, Rash or multiple lesions
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Orphanet: Von Hippel Lindau disease
The portal for rare diseases and orphan drugs
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=892
Welcome to PhenoDisWelcome to PhenoDis
Visceral angiomatosis. Very frequent [Orphanet] 21 / 7739 47. (HPO:0000822) Hypertension. Occasional [Orphanet] 224 / 7739 ...
http://mips.helmholtz-muenchen.de/phenodis/disease/show/883
Dani S. Zander, MDDani S. Zander, MD
Case report: bacillary angiomatosis with massive visceral lymphadenopathy. The American journal of the medical sciences, 306 4 ...
https://www.med.uc.edu/depart/pathology/directory/faculty-profile/Index/Pubs/zanderds
LOINC LP14083-7 - Bartonella henselaeLOINC LP14083-7 - Bartonella henselae
Synonyms: angiomatosis bacilar;. B henselae;. CSD;. Enfermedad por arañazo de gato;. Fiebre por arañazo de gato;. peliosis ...
https://loinc.org/LP14083-7/
World Infectious Disease Testing MarketWorld Infectious Disease Testing Market
7. Bacillary Epithelioid Angiomatosis (BEA) and Other Bartonella (Rochalimaea). 8. Blastocystis Hominis. 9. Brucella. 10. ...
https://www.aarkstore.com/healthcare/1874219/world-infectious-disease-testing-market
Todd Michael Cooper, DOTodd Michael Cooper, DO
Bacillary Angiomatosis in Patients With Cancer: A Pediatric Case Report and a Review of the Literature.. 26619465 Journal of ... Bacillary Angiomatosis in Patients With Cancer: A Pediatric Case Report and a Review of the Literature.. 26619465 Journal of ...
https://www.seattlechildrens.org/directory/todd-michael-cooper/
Encephalocraniocutaneous lipomatosis | Radiology Reference Article | Radiopaedia.orgEncephalocraniocutaneous lipomatosis | Radiology Reference Article | Radiopaedia.org
Sturge-Weber syndrome (encephalotrigeminal angiomatosis). * von Hippel-Lindau disease (retinocerebellar angiomatosis , mnemonic ...
https://radiopaedia.org/articles/encephalocraniocutaneous-lipomatosis
Doctor - ISHRSDoctor - ISHRS
Bacillary angiomatosis of AIDS: a case report and review of the literature. Journal of American Academy of Dermatology1990; 22: ...
https://ishrs.org/doctor/13849/
Connective Tissue Tumors in Animals - Integumentary System - Merck Veterinary ManualConnective Tissue Tumors in Animals - Integumentary System - Merck Veterinary Manual
Except in dairy cattle with angiomatosis, development of additional tumors at new sites after complete excision is uncommon. ... Dairy cattle are predisposed to developing disseminated hemangiomas (angiomatosis) in the skin and internal organs. ...
https://www.merckvetmanual.com/veterinary/integumentary-system/tumors-of-the-skin-and-soft-tissues/connective-tissue-tumors-in-animals
SciELO - Brazil - Oral Candida flora from Brazilian human immunodeficiency virus-infected patients in the highly active...SciELO - Brazil - Oral Candida flora from Brazilian human immunodeficiency virus-infected patients in the highly active...
Category B consists of symptomatic conditions in HIV-infected adolescent or adult such as bacillary angiomatosis, candidosis ...
https://www.scielo.br/j/mioc/a/nDnLMMDC7nLnGtW8PQmPrwN/?lang=en
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Gastrointestinal Pyogenic Granuloma (Lobular Capillary Hemangioma): An Underrecognized Entity Causing Iron Deficiency AnemiaGastrointestinal Pyogenic Granuloma (Lobular Capillary Hemangioma): An Underrecognized Entity Causing Iron Deficiency Anemia
... the main pathological differential diagnosis of PG includes bacillary angiomatosis (BA), Kaposis sarcoma (KS), or inflammatory ...
https://www.hindawi.com/journals/crigm/2016/4398401/
Bacillary angiomatosisDermalDiffuseLeptomeningeal angiomatosisBacilarEncephalotrigeminalEncephalotrigeminalEndocarditisCutaneousBartonellaEncephalofacialCause of bacillary angiomatosisLesions of bacillary angiomatosisQuintanaVisceralHenselaeRetinal angiomatosisEpithelioid angiomatosisDiseaseProliferationRetinaeDiagnosisKaposiPatientsAIDSManifestationsReactiveClinicalErythromycinSkinCaseReport
Bacillary angiomatosis28
  • Bacillary angiomatosis is a vascular, proliferative form of Bartonella infection that primarily occurs in immunocompromised persons. (medscape.com)
  • Bacillary angiomatosis is the second-most-common cause of angiomatous skin lesions in persons infected with the human immunodeficiency virus (HIV). (medscape.com)
  • Patients with bacillary angiomatosis commonly have a history of HIV infection, organ transplantation, leukemia, or chemotherapy. (medscape.com)
  • The diagnosis of cutaneous bacillary angiomatosis and extracutaneous disease is most often based on clinical features coupled with biopsies of lesions. (medscape.com)
  • Computed tomography (CT) scanning of the brain can detect intracerebral bacillary angiomatosis. (medscape.com)
  • Bacillary angiomatosis can be cured in most patients with antibiotics. (medscape.com)
  • The reader is referred to the 2014 guidelines published by the Infectious Diseases Society of America (IDSA) for the treatment of bacillary angiomatosis (see Practice Guidelines for the Diagnosis and Management of Skin and Soft Tissue Infections: 2014 Update by the Infectious Diseases Society of America ). (medscape.com)
  • The search for the infectious agents responsible for cat-scratch disease, bacillary angiomatosis, and related syndromes has a long and often circuitous history. (cdc.gov)
  • Is body wraps and electrical treatments contraindicated for bacillary angiomatosis? (salon-compass.com)
  • Is bacillary angiomatosis contagious? (salon-compass.com)
  • How to treat bacillary angiomatosis? (sage-advices.com)
  • Oral erythromycin remains the drug of choice for bacillary angiomatosis, with skin lesions often gradually fading over a period of 4 weeks. (sage-advices.com)
  • How do you get bacillary angiomatosis? (sage-advices.com)
  • Bacillary angiomatosis (epithelioid angiomatosis) is an uncommon disease characterized by neovascular proliferation in the skin or the internal organs (peliosis) due to an infection with Bartonella henselae or Bartonella quintana. (sage-advices.com)
  • What causes bacillary angiomatosis? (sage-advices.com)
  • Bacillary angiomatosis is skin infection caused by the gram-negative bacteria Bartonella henselae or B. quintana. (sage-advices.com)
  • Visceral involvement associated with bacillary angiomatosis may be asymptomatic or may cause the following symptoms: Fever, chills, malaise, night sweats, anorexia, and weight loss. (sage-advices.com)
  • How can you tell the difference between Kaposi sarcoma and bacillary angiomatosis? (sage-advices.com)
  • Bacillary angiomatosis lesions typically possess capillary proliferation and neutrophilic inflammation. (sage-advices.com)
  • Does bacillary angiomatosis blanch? (sage-advices.com)
  • Cockerell, CJ 1995, ' Bacillary angiomatosis and related diseases caused by Rochalimaea ', Journal of the American Academy of Dermatology , vol. 32, no. 5 PART 1, pp. 783-790. (elsevier.com)
  • Bartonella quintana may cause endocardistis, bacillary angiomatosis and or trench fever in humans. (petplace.com)
  • The answer to the mystery quiz is bacillary angiomatosis (BA). (clinicalcorrelations.org)
  • There are multiple clinical forms of cutaneous lesions in bacillary angiomatosis including dermal and subcutaneous nodules. (clinicalcorrelations.org)
  • 1. Cotell S, Noskin G. Bacillary angiomatosis: clinical and histologic features, diagnosis and treatment. (clinicalcorrelations.org)
  • 3. Wong R. Bacillary angiomatosis and other Bartonella species infections. (clinicalcorrelations.org)
  • Bacillary angiomatosis also known as Cat scratch disease by : Bartonella spp. (medicinembbs.com)
  • A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS , or reactive vascular proliferations, such as in bacillary angiomatosis. (bvsalud.org)
Dermal4
  • What is diffuse dermal angiomatosis? (sage-advices.com)
  • Diffuse dermal angiomatosis (DDA) is a rare skin condition that commonly presents as erythematous, violaceous, indurated plaques on the lower extremities of patients with severe peripheral vascular disease. (sage-advices.com)
  • Diffuse dermal angiomatosis: a rare cause of painful ulceration in renal insufficiency. (bvsalud.org)
  • Diffuse dermal angiomatosis is a rare, benign, reactive cutaneous vascular proliferation that has been reported in the context of end-stage renal failure and can rarely be associated with arteriovenous fistulas . (bvsalud.org)
Diffuse1
  • Angiomatosis is a diffuse vascular lesion which clinically mimics hemangioma or vascular malformation. (sage-advices.com)
Leptomeningeal angiomatosis5
  • IMSEAR at SEARO: Incomplete monosymptomatic leptomeningeal angiomatosis. (who.int)
  • Incomplete monosymptomatic leptomeningeal angiomatosis. (who.int)
  • Our case qualifies to be called incomplete monosymptomatic leptomeningeal angiomatosis. (who.int)
  • What is Leptomeningeal Angiomatosis? (sage-advices.com)
  • Leptomeningeal angiomatosis is a congenital vascular anomaly characterized by venous angiomas of leptomeninges. (sage-advices.com)
Bacilar1
  • Afeción que presenta múltiples lesiones parecidas a tumores, que pueden ser congénitas o producidas durante el desarrollo de los VASOS SANGUÍNEOS, o tratarse de proliferaciones vasculares reactivas, como sería el caso de la angiomatosis bacilar. (bvsalud.org)
Encephalotrigeminal1
  • Introduction: The Sturge-Weber Syndrome, also known as encephalotrigeminal angiomatosis, is a rare vascular neurocutaneous alteration. (bvsalud.org)
Encephalotrigeminal3
  • Taber's Online , www.tabers.com/tabersonline/view/Tabers-Dictionary/730377/all/encephalotrigeminal_angiomatosis. (tabers.com)
  • This case is an illustration of the ability of the cerebral angiogram to highlight the pathoanatomy of the Sturge-Weber Syndrome (SWS), also known as Encephalotrigeminal Angiomatosis. (neuroangio.org)
  • Introduction: The Sturge-Weber Syndrome, also known as encephalotrigeminal angiomatosis, is a rare vascular neurocutaneous alteration. (bvsalud.org)
Endocarditis5
  • B henselae has been associated with cat scratch disease, bacillary angiomatosis, peliosis hepatitis, and endocarditis. (mayocliniclabs.com)
  • B quintana has been associated with trench fever, bacillary angiomatosis, and endocarditis. (mayocliniclabs.com)
  • Other more serious complications include chronic bactremia (a continuous presence of bacteria in the bloodstream), endocarditis (an infection of the inner lining of the heart chambers and valves), and, among immunocompromised people, a condition known as bacillary angiomatosis, characterized by lesions on the skin or internal organs. (health.com)
  • Immunocompromised patients, such as those with HIV, can develop more serious manifestations such as endocarditis and bacillary angiomatosis (tumor-like masses caused by the pathological proliferation of blood vessels). (columbia-lyme.org)
  • Menu of diseases caused by Bartonella includes cat scratch disease, retinitis, trench fever, Carrión's disease [Oroyo fever and verruga peruana], relapsing bacteremia, endocarditis, bacillary angiomatosis, and bacillary peliosis hepatitis. (hopkinsguides.com)
Cutaneous4
  • Cutaneous bacillary angiomatosis in renal transplant recipients: report of three new cases and literature review. (medscape.com)
  • Cutaneous nodules and hepatosplenic lesions caused by bacillary angiomatosis in a patient with AIDS. (nih.gov)
  • Diffuse dermal angiomatosis is a rare disorder, considered to be a variant of reactive cutaneous angioendotheliomatosis. (amegroups.com)
  • 9. AIDS presenting with cutaneous Kaposi's sarcoma and bacillary angiomatosis in the bone marrow mimicking Kaposi's sarcoma. (nih.gov)
Bartonella6
  • The organisms causing bacillary angiomatosis resemble the agent of verruga peruana and Oroya fever, Bartonella bacilliformis, in producing a histologically similar vascular proliferation, in having a gram-negative wall structure (as observed using electron microscopy), and in tending to grow in clumps visible by light microscopy. (medscape.com)
  • Molecular detection of Bartonella henselae for the diagnosis of cat scratch disease and bacillary angiomatosis of the conjunctiva. (medscape.com)
  • Bacillary Angiomatosis Bacillary angiomatosis is skin infection caused by the gram-negative bacteria Bartonella henselae or B. quintana. (merckmanuals.com)
  • A secondary tissue phase can be associated with development of vasculoproliferative lesions, e.g. bacillary angiomatosis ( Bartonella henselae, B. quintana ) or verruga peruana ( B. bacilliformis ) and may play a role in various other dermal conditions [ 3 - 7 ]. (biomedcentral.com)
  • Bacillary angiomatosis also known as Cat scratch disease by : Bartonella spp. (medicinembbs.com)
  • Bartonella organisms can sometimes be visualized by immunohistochemical staining, although this method of diagnosis is usually reserved for patients with angiomatosis. (lymeeducation.com)
Encephalofacial1
  • Encephalofacial angiomatosis (Sturge-Weber syndrome, Fig 14-10), racemose angioma (Wyburn-Mason syndrome, Fig 14-11), incontinentia pigmenti, and Klippel-Trénaunay-Weber syndrome are among the other conditions sometimes classified as phakomatoses. (aao.org)
Cause of bacillary angiomatosis1
  • The cause of bacillary angiomatosis is a previously uncharacterized rickettsia-like organism, closely related to R. quintana. (nih.gov)
Lesions of bacillary angiomatosis1
  • Because the 2 diseases may coexist, the lesions of bacillary angiomatosis may be easily overlooked. (medscape.com)
Quintana3
  • According to a report from Chile, a patient with HIV infection and bacillary angiomatosis caused by B quintana responded favorably to azithromycin plus ciprofloxacin started together with antiretroviral therapy. (medscape.com)
  • These 16S sequences associated with bacillary angiomatosis belong to a previously uncharacterized microorganism, most closely related to Rochalimaea quintana. (nih.gov)
  • 14. [Bacillary angiomatosis related to Rochalimaea quintana. (nih.gov)
Visceral2
  • Bacillary angiomatosis is an infectious disease causing proliferation of small blood vessels in the skin and visceral organs of patients with human immunodeficiency virus infection and other immunocompromised hosts. (nih.gov)
  • In 1904, von Hippel, a German ophthalmologist, described two patients with retinal angiomatosis, 1 and in 1926, Lindau, a Swedish neurologist, described an association among retinal angiomatosis, hemangiomatous cysts of the cerebellum, and the visceral components of the disease. (aafp.org)
Henselae1
  • Rare complications of B. henselae infection are bacillary angiomatosis and Parinaud's oculolandular syndrome. (asthmahealthcenter.com)
Retinal angiomatosis1
  • Coexistance of unilateral retionoblastoma and Leber's syndrome (retinal angiomatosis) in contralateral eye - case report. (krakow.pl)
Epithelioid angiomatosis2
  • Cockerell CJ, Bergstresser PR, Myrie-Williams C, Tierno PM. Bacillary epithelioid angiomatosis occurring in an immunocompetent individual. (medscape.com)
  • 6. [Bacillary epithelioid angiomatosis in advanced HIV infection]. (nih.gov)
Disease5
  • Bacillary angiomatosis, however, causes a vascular proliferation, not a formation of stellate abscesses without granuloma formation, as found in cat scratch disease. (medscape.com)
  • In addition, unlike patients with bacillary angiomatosis, those with cat scratch disease do not respond to antibiotics. (medscape.com)
  • The search for the infectious agents responsible for cat-scratch disease, bacillary angiomatosis, and related syndromes has a long and often circuitous history. (cdc.gov)
  • 12. Bacillary angiomatosis associated with extensive esophageal polyposis: a new mucocutaneous manifestation of acquired immunodeficiency disease (AIDS). (nih.gov)
  • 13. [Cat-scratch disease and bacillary angiomatosis. (nih.gov)
Proliferation1
  • Diffuse dermal angiomatosis (DDA) is a rare disorder of excess vascular proliferation characterized clinically by breast pain and benign violaceous, erythematous plaques with central ulcerations. (amegroups.com)
Retinae2
  • Brandt also described one other patient with angiomatosis retinae, who had died of brain tumor. (neurosurgery.tv)
  • A search of the literature revealed that in at least 10 percent of all cases of angiomatosis retinae. (neurosurgery.tv)
Diagnosis2
  • Results of punch biopsies taken near ulcerating lesions and of the red reticular pattern confirmed the diagnosis of diffuse dermal angiomatosis. (amegroups.com)
  • 4. Molecular diagnosis of deep nodular bacillary angiomatosis and monitoring of therapeutic success. (nih.gov)
Kaposi1
  • Failure to distinguish Kaposi sarcoma from bacillary angiomatosis is problematic because bacillary angiomatosis, unlike Kaposi sarcoma, responds dramatically to antibiotic therapy. (medscape.com)
Patients2
  • Tissue from three unrelated patients with bacillary angiomatosis yielded a unique 16S gene sequence. (nih.gov)
  • A sequence obtained from a fourth patient with bacillary angiomatosis differed from the sequence found in the other three patients at only 4 of 241 base positions. (nih.gov)
AIDS3
  • Bacillary angiomatosis of the cervix and vulva in a patient with AIDS. (nih.gov)
  • In persons with AIDS and bacillary angiomatosis, the primary pharmaceutical choices include erythromycin, doxycycline, or more expensive drugs such as azithromycin, clarithromycin, or a fluoroquinolone. (medscape.com)
  • 3. [Bacillary angiomatosis of the oral cavity in AIDS. (nih.gov)
Manifestations1
  • Iraji F, Pourazizi M, Abtahi-Naeini B, Meidani M, Rajabi P. Bacillary Angiomatosis in Immunocompetent Patient with Atypical Manifestations. (medscape.com)
Reactive1
  • A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS , or reactive vascular proliferations, such as in bacillary angiomatosis. (nih.gov)
Clinical1
  • The "Angiomatosis: Pipeline Review, Developer Landscape and Competitive Insights, 2021-2031" report features an extensive study on the marketed, clinical and preclinical molecules available / being developed for the treatment of Angiomatosis. (businessorgs.com)
Erythromycin1
  • Oral erythromycin remains the drug of choice for bacillary angiomatosis, with skin lesions often gradually fading over a period of 4 weeks. (medscape.com)
Skin1
  • Novel discoveries include the first identification of total body irradiation as a risk factor for skin fibrosis in chronic GVHD, the first comprehensive description of GVHD-associated angiomatosis, and the first link between voriconazole exposure and squamous cell carcinoma in allogeneic hematopoietic cell transplant recipients. (nih.gov)
Case1
  • A case of bacillary angiomatosis developed at a burn site. (medscape.com)
Report2
  • Herein, we report a patient who presented with unbearable bilateral breast pain with characteristic "reticular vascular marking" of her breasts, who was diagnosed with diffuse dermal angiomatosis. (amegroups.com)
  • 16. [Bacillary angiomatosis: report of 2 cases]. (nih.gov)
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