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.
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.
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.
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.
A family of small, gram-negative organisms, often parasitic in humans and other animals, causing diseases that may be transmitted by invertebrate vectors.
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.
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.
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.
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.
Infections with bacteria of the family RICKETTSIACEAE.
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.
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.
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.
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.
Diseases of BONES.
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.
Bone in humans and primates extending from the SHOULDER JOINT to the ELBOW JOINT.

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)

Angiomatosis is a medical term that refers to a benign condition characterized by the proliferation of blood vessels in various tissues and organs. It is typically composed of small, tangled blood vessels called capillaries, which can form clusters or networks. The condition can affect skin, internal organs, bones, and other tissues.

Angiomatosis is often asymptomatic and may be discovered incidentally during medical imaging or surgical procedures. In some cases, it may cause symptoms such as pain, swelling, or bleeding, depending on the location and extent of the lesions.

While angiomatosis is generally a benign condition, in rare cases, it can be associated with malignant tumors or other medical conditions. Treatment options for angiomatosis depend on the size, location, and symptoms of the lesions and may include observation, medication, or surgical removal.

Bacillary angiomatosis is a medical condition caused by infection with the bacteria Bartonella henselae or Bartonella quintana. It is characterized by the growth of blood vessel tissue in various parts of the body, leading to the formation of lesions or tumors. These lesions can appear as red papules or nodules on the skin, and can also affect internal organs such as the liver, spleen, and lymph nodes.

The condition is typically seen in individuals with weakened immune systems, such as those with HIV/AIDS, and can be treated with antibiotics. It is important to note that bacillary angiomatosis should not be confused with other forms of angiomatosis or vascular tumors, which have different causes and treatments.

Bartonella quintana is a gram-negative, aerobic bacillus that is the causative agent of trench fever, a disease first described during World War I. The bacterium is primarily transmitted to humans through the feces of body lice, and it can also cause endocarditis and other systemic infections.

The name "quintana" refers to the characteristic fever pattern of the disease, which features recurring episodes every fifth day. Other symptoms of trench fever include headache, muscle pain, and a rash. The disease is typically treated with antibiotics, such as doxycycline or azithromycin.

Bartonella quintana is also known to cause cat scratch disease in immunocompromised individuals. It can be transmitted through the scratches or bites of cats infected with the bacterium. The symptoms of cat scratch disease include fever, swollen lymph nodes, and fatigue.

Overall, Bartonella quintana is a significant public health concern, particularly in populations with poor hygiene and crowded living conditions, such as homeless individuals and refugees.

'Bartonella henselae' is a gram-negative bacterium that is the primary cause of cat scratch disease (CSD) in humans. The bacteria are transmitted through the scratch or bite of an infected cat, or more rarely, through contact with cat saliva on a wound or mucous membrane.

Infected individuals may experience mild to severe symptoms, including fever, headache, fatigue, and lymph node swelling near the site of infection. In some cases, the bacteria can spread to other parts of the body, causing more serious complications such as endocarditis (inflammation of the inner lining of the heart), encephalopathy (brain damage), or neurological symptoms.

Diagnosis of Bartonella henselae infection typically involves a combination of clinical symptoms, serological testing, and sometimes molecular methods such as PCR. Treatment usually consists of antibiotics, with doxycycline being the first-line therapy for adults and macrolides for children. In severe cases, intravenous antibiotics may be necessary.

Preventive measures include avoiding contact with cats' claws and saliva, particularly if you have a weakened immune system, and practicing good hygiene after handling cats or their litter boxes.

Rickettsiaceae is a family of Gram-negative, obligate intracellular bacteria that are primarily parasitic in arthropods and mammals. They are the causative agents of several important human diseases, including typhus fever, Rocky Mountain spotted fever, and rickettsialpox. These bacteria are typically transmitted to humans through the bites of infected arthropods such as ticks, fleas, or lice.

The bacteria in Rickettsiaceae are small, non-motile, and have a unique bipolar appearance with tapered ends. They can only replicate inside host cells, where they manipulate the host cell's machinery to create a protective niche for themselves. This makes them difficult to culture and study outside of their hosts.

Rickettsiaceae bacteria are divided into several genera based on their genetic and antigenic characteristics, including Rickettsia, Orientia, and Coxiella. Each genus contains several species that can cause different diseases in humans. For example, Rickettsia rickettsii is the causative agent of Rocky Mountain spotted fever, while Rickettsia prowazekii causes epidemic typhus.

Overall, Rickettsiaceae bacteria are important pathogens that can cause serious and sometimes fatal diseases in humans. Prompt diagnosis and treatment with appropriate antibiotics is essential for a successful outcome.

Essential osteolysis is not a well-defined medical condition with a single, widely accepted medical definition. The term "osteolysis" generally refers to the loss or resorption of bone tissue. In essential osteolysis, this process occurs without an underlying cause that can be easily identified, such as a tumor, infection, or other disease.

Some sources describe essential osteolysis as a condition characterized by progressive bone loss that occurs spontaneously and symmetrically, typically affecting the small bones of the hands and feet. The exact cause of this form of osteolysis is not known, but it is thought to be related to an abnormal immune response or genetic factors.

It's important to note that essential osteolysis is a rare condition, and its symptoms and progression can vary significantly from person to person. If you have concerns about osteolysis or any other medical condition, it's best to consult with a healthcare professional for an accurate diagnosis and treatment plan.

Trench fever is a historical medical condition that primarily affected soldiers during World War I. It is caused by Bartonella quintana, a type of bacterium that is transmitted through the feces of body lice. The name "trench fever" comes from the fact that it was common among soldiers living in trenches, where poor hygiene and crowded conditions facilitated the spread of the disease.

Symptoms of trench fever include sudden onset of fever, severe headache, muscle pain, and a rash. The fever typically lasts for about five days and then recurs every four to six days, which is why it was also known as "five-day fever" or "recrudescence fever." Other symptoms can include fatigue, anemia, and swelling of the spleen and liver.

Trench fever is treated with antibiotics such as doxycycline or azithromycin. Prevention measures include good personal hygiene, such as regular bathing and changing clothes, as well as environmental controls to reduce louse populations, such as delousing stations and insecticides.

While trench fever is no longer a major public health concern, it remains an important historical medical condition that highlights the importance of hygiene and infection control in military settings.

Cat-scratch disease (CSD) is a bacterial infection caused by Bartonella henselae. It is typically transmitted through contact with a cat, especially when the animal scratches or bites a person and then introduces the bacteria into the wound. The incubation period for CSD is usually 7-14 days after exposure.

The most common symptoms of CSD include:

* A small, raised bump (called a papule) that develops at the site of the scratch or bite within a few days of being scratched or bitten by a cat. This bump may be tender and can sometimes form a crust or pustule.
* Swollen lymph nodes (also called lymphadenopathy) near the site of the infection, which usually develop 1-2 weeks after the initial scratch or bite. These swollen lymph nodes are often painful and may be warm to the touch.
* Fatigue, fever, headache, and muscle aches are also common symptoms of CSD.

In most cases, cat-scratch disease is a mild illness that resolves on its own within a few weeks or months. However, in some cases, it can cause more severe complications, such as infection of the heart valves (endocarditis), inflammation of the brain (encephalitis), or damage to the eyes (retinitis).

Treatment for cat-scratch disease typically involves supportive care, such as pain relief and anti-inflammatory medications. Antibiotics may be prescribed in some cases, particularly if the infection is severe or if the patient has a weakened immune system. Preventive measures include washing hands after handling cats, avoiding rough play with cats, and promptly treating cat bites and scratches.

Peliosis hepatis is a rare condition characterized by the presence of numerous blood-filled cavities or sinusoids in the liver. These cavities can vary in size and are usually distributed throughout the liver parenchyma. The term "peliosis" comes from the Greek word "pelios," which means "bluish-black."

In peliosis hepatis, these blood-filled spaces can rupture, leading to bleeding into the liver tissue or even into the abdominal cavity. This condition is often asymptomatic but may present with nonspecific symptoms such as fatigue, weakness, abdominal pain, or liver dysfunction.

Peliosis hepatis has been associated with various conditions, including blood disorders (such as leukemia and lymphoma), use of anabolic steroids, immunosuppressive therapy, chronic infections (such as HIV and tuberculosis), and certain malignancies. In many cases, the cause remains unknown, and the condition is referred to as idiopathic peliosis hepatis.

Diagnosis of peliosis hepatis typically requires imaging studies such as computed tomography (CT) or magnetic resonance imaging (MRI), which can demonstrate the presence of multiple, round, blood-filled spaces in the liver. In some cases, a liver biopsy may be necessary to confirm the diagnosis and evaluate the severity of the condition. Treatment depends on the underlying cause and may include discontinuation of any offending medications or treatment of any underlying conditions.

Rickettsiaceae is a family of Gram-negative, aerobic, intracellular bacteria that includes several important human pathogens. Rickettsiaceae infections are diseases caused by these bacteria, which include:

1. Rocky Mountain Spotted Fever (RMSF): Caused by Rickettsia rickettsii and transmitted to humans through the bite of infected ticks. The disease is characterized by fever, headache, muscle pain, and a rash that spreads from the wrists and ankles to the trunk.
2. Epidemic Typhus: Caused by Rickettsia prowazekii and transmitted to humans through the feces of infected lice. The disease is characterized by fever, headache, muscle pain, and a rash that starts on the chest and spreads to the rest of the body.
3. Murine Typhus: Caused by Rickettsia typhi and transmitted to humans through the feces of infected fleas. The disease is characterized by fever, headache, muscle pain, and a rash that starts on the trunk and spreads to the limbs.
4. Scrub Typhus: Caused by Orientia tsutsugamushi and transmitted to humans through the bite of infected chiggers. The disease is characterized by fever, headache, muscle pain, and a rash that starts on the trunk and spreads to the limbs.
5. Rickettsialpox: Caused by Rickettsia akari and transmitted to humans through the bite of infected mites. The disease is characterized by fever, headache, muscle pain, and a rash that starts as papules and becomes vesicular.

These infections are treated with antibiotics such as doxycycline or chloramphenicol. Early diagnosis and treatment are crucial to prevent severe complications and death.

Bartonella infections are a group of diseases caused by bacteria belonging to the Bartonella genus. These gram-negative bacteria can infect humans and animals, causing various symptoms depending on the specific Bartonella species involved. Some common Bartonella infections include:

1. Cat scratch disease (Bartonella henselae): This is the most common Bartonella infection, usually transmitted through contact with a cat's scratch or saliva. The primary symptom is a tender, swollen lymph node near the site of the scratch. Other symptoms may include fever, fatigue, and headache.
2. Trench fever (Bartonella quintana): This infection was first identified during World War I among soldiers living in trenches, hence its name. It is primarily transmitted through the feces of body lice. Symptoms include fever, severe headaches, muscle pain, and a rash.
3. Carrion's disease (Bartonella bacilliformis): This infection is endemic to South America, particularly in the Andean regions of Peru, Ecuador, and Colombia. It is transmitted through the bite of sandflies. The acute phase of the disease, known as Oroya fever, is characterized by high fever, severe anemia, and potentially life-threatening complications. The chronic phase, known as verruga peruana, presents with skin lesions resembling warts or boils.

Diagnosis of Bartonella infections typically involves blood tests to detect antibodies against the bacteria or direct detection of the bacterial DNA using PCR techniques. Treatment usually consists of antibiotics such as azithromycin, doxycycline, or rifampin, depending on the specific infection and severity of symptoms.

"Bartonella" is a genus of gram-negative bacteria that are facultative intracellular pathogens, meaning they can live and multiply inside host cells. They are the cause of several emerging infectious diseases in humans and animals. Some species of Bartonella are associated with clinical syndromes such as cat scratch disease, trench fever, and Carrion's disease. The bacteria are transmitted to humans through the bites or feces of insect vectors (such as fleas, lice, and sandflies) or through contact with infected animals. Once inside the host, Bartonella can evade the immune system and cause chronic infection, which can lead to a variety of clinical manifestations, including fever, fatigue, lymphadenopathy, endocarditis, and neurological symptoms.

The medical definition of 'Bartonella' is: A genus of fastidious, gram-negative bacteria that are facultative intracellular pathogens. Bartonella species are the cause of several emerging infectious diseases in humans and animals. The bacteria are transmitted to humans through the bites or feces of insect vectors (such as fleas, lice, and sandflies) or through contact with infected animals. Bartonella species can evade the immune system and cause chronic infection, leading to a variety of clinical manifestations, including fever, fatigue, lymphadenopathy, endocarditis, and neurological symptoms.

Sturge-Weber syndrome is a rare neurocutaneous disorder characterized by the combination of a facial port-wine birthmark and neurological abnormalities. The facial birthmark, which is typically located on one side of the face, occurs due to the malformation of small blood vessels (capillaries) in the skin and eye.

Neurological features often include seizures that begin in infancy, muscle weakness or paralysis on one side of the body (hemiparesis), developmental delay, and intellectual disability. These neurological symptoms are caused by abnormal blood vessel formation in the brain (leptomeningeal angiomatosis) leading to increased pressure, reduced blood flow, and potential damage to the brain tissue.

Sturge-Weber syndrome can also affect the eyes, with glaucoma being a common occurrence due to increased pressure within the eye. Early diagnosis and appropriate management of this condition are crucial for improving the quality of life and reducing potential complications.

A bone cyst is a fluid-filled sac that develops within a bone. It can be classified as either simple (unicameral) or aneurysmal. Simple bone cysts are more common in children and adolescents, and they typically affect the long bones of the arms or legs. These cysts are usually asymptomatic unless they become large enough to weaken the bone and cause a fracture. Aneurysmal bone cysts, on the other hand, can occur at any age and can affect any bone, but they are most common in the leg bones and spine. They are characterized by rapidly growing blood-filled sacs that can cause pain, swelling, and fractures.

Both types of bone cysts may be treated with observation, medication, or surgery depending on their size, location, and symptoms. It is important to note that while these cysts can be benign, they should still be evaluated and monitored by a healthcare professional to ensure proper treatment and prevention of complications.

Bone diseases is a broad term that refers to various medical conditions that affect the bones. These conditions can be categorized into several groups, including:

1. Developmental and congenital bone diseases: These are conditions that affect bone growth and development before or at birth. Examples include osteogenesis imperfecta (brittle bone disease), achondroplasia (dwarfism), and cleidocranial dysostosis.
2. Metabolic bone diseases: These are conditions that affect the body's ability to maintain healthy bones. They are often caused by hormonal imbalances, vitamin deficiencies, or problems with mineral metabolism. Examples include osteoporosis, osteomalacia, and Paget's disease of bone.
3. Inflammatory bone diseases: These are conditions that cause inflammation in the bones. They can be caused by infections, autoimmune disorders, or other medical conditions. Examples include osteomyelitis, rheumatoid arthritis, and ankylosing spondylitis.
4. Degenerative bone diseases: These are conditions that cause the bones to break down over time. They can be caused by aging, injury, or disease. Examples include osteoarthritis, avascular necrosis, and diffuse idiopathic skeletal hyperostosis (DISH).
5. Tumors and cancers of the bone: These are conditions that involve abnormal growths in the bones. They can be benign or malignant. Examples include osteosarcoma, chondrosarcoma, and Ewing sarcoma.
6. Fractures and injuries: While not strictly a "disease," fractures and injuries are common conditions that affect the bones. They can result from trauma, overuse, or weakened bones. Examples include stress fractures, compound fractures, and dislocations.

Overall, bone diseases can cause a wide range of symptoms, including pain, stiffness, deformity, and decreased mobility. Treatment for these conditions varies depending on the specific diagnosis but may include medication, surgery, physical therapy, or lifestyle changes.

AIDS-related opportunistic infections (AROIs) are infections that occur more frequently or are more severe in people with weakened immune systems, such as those with advanced HIV infection or AIDS. These infections take advantage of a weakened immune system and can affect various organs and systems in the body.

Common examples of AROIs include:

1. Pneumocystis pneumonia (PCP), caused by the fungus Pneumocystis jirovecii
2. Mycobacterium avium complex (MAC) infection, caused by a type of bacteria called mycobacteria
3. Candidiasis, a fungal infection that can affect various parts of the body, including the mouth, esophagus, and genitals
4. Toxoplasmosis, caused by the parasite Toxoplasma gondii
5. Cryptococcosis, a fungal infection that affects the lungs and central nervous system
6. Cytomegalovirus (CMV) infection, caused by a type of herpes virus
7. Tuberculosis (TB), caused by the bacterium Mycobacterium tuberculosis
8. Cryptosporidiosis, a parasitic infection that affects the intestines
9. Progressive multifocal leukoencephalopathy (PML), a viral infection that affects the brain

Preventing and treating AROIs is an important part of managing HIV/AIDS, as they can cause significant illness and even death in people with weakened immune systems. Antiretroviral therapy (ART) is used to treat HIV infection and prevent the progression of HIV to AIDS, which can help reduce the risk of opportunistic infections. In addition, medications to prevent specific opportunistic infections may be prescribed for people with advanced HIV or AIDS.

The humerus is the long bone in the upper arm that extends from the shoulder joint (glenohumeral joint) to the elbow joint. It articulates with the glenoid cavity of the scapula to form the shoulder joint and with the radius and ulna bones at the elbow joint. The proximal end of the humerus has a rounded head that provides for movement in multiple planes, making it one of the most mobile joints in the body. The greater and lesser tubercles are bony prominences on the humeral head that serve as attachment sites for muscles that move the shoulder and arm. The narrow shaft of the humerus provides stability and strength for weight-bearing activities, while the distal end forms two articulations: one with the ulna (trochlea) and one with the radius (capitulum). Together, these structures allow for a wide range of motion in the shoulder and elbow joints.

Angiomatosis is a non-neoplastic condition characterised by nests of proliferating capillaries arranged in a lobular pattern, ... "angiomatosis" at Dorlands 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 ...
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 ...
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 ...
Find symptoms and other information about Diffuse dermal angiomatosis. ... About Diffuse dermal angiomatosis. Many rare diseases have limited information. Currently GARD aims to provide the following ... When Do Symptoms of Diffuse dermal angiomatosis Begin?. This section is currently in development. ...
... such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic. ... "Angiomatosis" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... This graph shows the total number of publications written about "Angiomatosis" by people in this website by year, and whether " ... Diffuse dermal angiomatosis associated with calciphylaxis. Am J Dermatopathol. 2009 Oct; 31(7):653-7. ...
Bacillary Angiomatosis - Etiology, pathophysiology, symptoms, signs, diagnosis & prognosis from the MSD Manuals - Medical ... Bacillary Angiomatosis (Epithelioid Angiomatosis). By Larry M. Bush , MD, FACP, Charles E. Schmidt College of Medicine, Florida ... Bacillary angiomatosis is skin infection caused by the gram-negative bacteria Bartonella henselae or B. quintana. Diagnosis is ... Treatment of bacillary angiomatosis is with oral erythromycin 500 mg every 6 hours or oral doxycycline 100 mg every 12 hours, ...
Bacillary Angiomatosis (Angiomatoses Bacillary): Read more about Symptoms, Diagnosis, Treatment, Complications, Causes and ... Bacillary angiomatosis is a benign proliferative disorder of capillaries caused by bacteria pertaining to the genus of ... Angiomatoses Bacillary Bacillary angiomatosis is a benign proliferative disorder of capillaries caused by bacteria pertaining ... Bacillary angiomatosis should be kept in mind in the differential diagnosis of leg ulcers in cases of unknown aetiology. [ncbi. ...
Bacillary angiomatosis is no exception to this rule. Bacillary angiomatosis is a cutaneous and systemic bacterial infection ... Bacillary angiomatosis is a cutaneous and systemic bacterial infection caused by gram-negative Bartonella species. We report a ... a case of an immunocompromised 44 years old female patient who presented with a solitary tumor-like bacillary angiomatosis that ... case of an immunocompromised 44 years old female patient who presented with a solitary tumor-like bacillary angiomatosis that ...
... bacillary angiomatosis, and infective endocarditis (3). Because the bacterium requires special conditions to grow in culture, ...
Bismuth subsalicylate four times daily reduces rates of travelers diarrhea.[2][26] Though many travelers find a four-times-per-day regimen inconvenient, lower doses have not been shown to be effective.[2][26] Potential side effects include black tongue, black stools, nausea, constipation, and ringing in the ears. Bismuth subsalicylate should not be taken by those with aspirin allergy, kidney disease, or gout, nor concurrently with certain antibiotics such as the quinolones, and should not be taken continuously for more than three weeks.[medical citation needed] Some countries do not recommend it due to the risk of rare but serious side effects.[26] A hyperimmune bovine colostrum to be taken by mouth is marketed in Australia for prevention of ETEC-induced TD. As yet, no studies show efficacy under actual travel conditions.[3] Though effective, antibiotics are not recommended for prevention of TD in most situations because of the risk of allergy or adverse reactions to the antibiotics, and ...
Adolescent, Adult, Angiomatosis, Child, Child, Preschool, Eye Neoplasms, Female, Fluorescein Angiography, Humans, Middle Aged, ...
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.
Included in these disorders are eosinophilic folliculitis, oral hairy leukoplakia, bacillary angiomatosis, and Kaposi sarcoma. ...
The key difference between Kaposi sarcoma and bacillary angiomatosis is that Kaposi sarcoma is a type of cancer caused by a ... What is Bacillary Angiomatosis?. Bacillary Angiomatosis is an uncommon disorder. It is also known as epithelioid angiomatosis. ... 3. What is Bacillary Angiomatosis. 4. Similarities - Kaposi Sarcoma vs Bacillary Angiomatosis. 5. Kaposi Sarcoma vs Bacillary ... What are the Similarities Between Kaposi Sarcoma and Bacillary Angiomatosis?. *Kaposi sarcoma and bacillary angiomatosis are ...
Cutaneous lesions of bacillary angiomatosis Images In Infectious Diseases. Keong, Seow Chee; Fu, Gan Wee; Hashim, Hasmah * Text ...
Keywords: Angiosarcoma; Congenital hemangioma; Cutaneovisceral angiomatosis with thrombocytopenia; Enzinger intramuscular ...
Diffuse dermal angiomatosis (DDA) is a rare, cutaneous vascular disorder described in 1994. Initially, it was thought to be a ... Diffuse dermal angiomatosis (DDA) is a rare, cutaneous vascular disorder described in 1994.1 Initially, it was thought to be a ... The Treatment of Diffuse Dermal Angiomatosis of the Breast With Reduction Mammaplasty. Arch Dermatol. 2008;144(5):693-694. doi: ... The Treatment of Diffuse Dermal Angiomatosis of the Breast With Reduction Mammaplasty. ...
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Angiomatosis Bacilar/inmunología Angiomatosis Bacilar/microbiología Infecciones por Bartonella/inmunología Infecciones por ... First Report of Bacillary Angiomatosis by Bartonella elizabethae in an HIV-Positive Patient.. Corral, Julieta; Manríquez Robles ... As far as we know, this is the first case of bacillary angiomatosis secondary to this etiological agent. ... developed polymorphous lesions in which the evidence in the skin biopsy corresponds to the diagnosis of bacillary angiomatosis ...
Bacillary angiomatosis *Candidiasis, oropharyngeal (thrush) *Candidiasis, vulvovaginal; persistent, frequent, or poorly ...
DIFFUSE DERMAL ANGIOMATOSIS. Diffuse Dermal Angiomatosis: A Previously Undescribed Pattern of Immunoglobulin and Complement ... Dermal angiomatosis of the breast is an extremely rare disorder of unknown origin characterized by increased angiomatosis and ... Two cases of diffuse dermal angiomatosis are reported in middle-aged women. This rare disease of unknown origin is ... characterized by increased dermal angiomatosis and ulceration. The clinical and histologic presentations of the presently ...
Cystic Angiomatosis. *Familial Dilated Cardiomyopathy. *Heart Attack. *Hyperlipidemia. *Mitral Valve Prolapse. *Peripheral ...
Giant bacillary angiomatosis. Nel, Jeremy; Ive, Prudence; Nel, Carolina. · texto em Inglês · Inglês ( pdf ) ...
Skeletal cystic angiomatosis: A rare cause of unilateral lytic bone lesions (Articles) ...
Vail D. Angiomatosis retinae, eleven years after diathermy coagulation. Am J Ophthalmol. 1958;46:525-534. ... Fifteen year review of treated cases of retinal angiomatosis. Trans Am Acad Ophthalmol Otolaryngol. 1977;83:446-453. ... Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation. Arch ... Fifteen year review of treated cases of retinal angiomatosis. Trans Am Acad Ophthalmol Otolaryngol. 1977;83:446-453. ...
7. Bacillary Epithelioid Angiomatosis (BEA) And Other. Bartonella (Rochalimaea). a. Background. b. Diagnostic Tests. c. ...
Bacillary angiomatosis is a rare opportunistic bacterial infection due to Bartonella henselae. ... Diffuse dermal angiomatosis of the breast: painful ulceration and telangiectases of pendulous breasts ...
The epidemiology of bacillary angiomatosis and bacillary peliosis. JAMA. 269(6): 770-775. ...

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