Other entities which are accompanied by multiple lipomas include Proteus syndrome, Cowden syndrome and related disorders due to PTEN gene mutations, benign symmetric lipomatosis (Madelung disease), Dercum's Disease, familial lipodystrophy, hibernomas, epidural steroid injections with epidural lipomatosis, and familial angiolipomatosis. (wikipedia.org)
Multiple symmetric lipomatosis (MSL) is a rare disease also known as Madelung's disease, Launois-Bensaude syndrome, and benign symmetric lipomatosis. (hindawi.com)
Multiple symmetric lipomatosis (MSL) is a rare disease characterized by the growth of uncapsulated masses of adipose tissue. (lipomaboard.com)
The man developed the rare condition known as multiple symmetric lipomatosis after drinking strong liquor every day for three decades. (ibtimes.co.in)
Multiple benign symmetric lipomatosis (Madelung s disease, Launois Bensaude syndrome) is significantly rare disease characterised by symmetrical focal deposition of adipose tissue in the neck, upper part of the arms, back, pelvis, and thigh. (endocrine-abstracts.org)
Multiple symmetric lipomatosis represents a group of similar syndromes characterized by the excessive growth of subcutaneous fat, often in the periphery of the body in areas such as the arms, legs, shoulders, and neck (picture the Michelin man). (scienceblogs.com)
For a given BMI, multiple symmetric lipomatosis patients are reported to carry 50% more fat tissue than healthy individuals. (scienceblogs.com)
Congenital5
Encephalocraniocutaneous lipomatosis (ECCL) comprises a spectrum of predominantly congenital anomalies. (nih.gov)
Encephalocraniocutaneous lipomatosis (ECCL) is a rare, congenital, neurocutaneous disorder with unilateral lipomatous cutaneous neoplasms devoid of hair and ipsilateral ophthalmologic and neurologic malformations. (medscape.com)
Could congenital infiltrating lipomatosis of the face have an anatomic explanation: Lipomatosis of the trigeminal nerve and nerve-territory overgrowth? (elsevierpure.com)
Dive into the research topics of 'Could congenital infiltrating lipomatosis of the face have an anatomic explanation: Lipomatosis of the trigeminal nerve and nerve-territory overgrowth? (elsevierpure.com)
Congenital infiltrating lipomatosis of the face: recognition and pathogenesis. (bvsalud.org)
Pelvic lipomatosis6
Pelvic lipomatosis - A rare disease most often seen in older obese black men with hypertension. (wikipedia.org)
Pelvic lipomatosis is a rare disorder of increased fat tissue deposition within the spaces of the pelvis, causing extrinsic compression of the bladder, rectum, and blood vessels. (radiologytoday.net)
Approximately one-half of patients with symptomatic pelvic lipomatosis present with lower urinary symptoms, such as increased frequency, dysuria, nocturia, and hesitancy. (radiologytoday.net)
On plain radiograph, pelvic lipomatosis appears as hyperlucent soft tissue mass within the pelvis. (radiologytoday.net)
Radiation therapy is not only unsuccessful in treating pelvic lipomatosis, but can also result in bladder outlet and rectal strictures.2 Urinary diversion procedures consisting of ileal conduit, nephrostomy tube, or vesicostomy may be required in cases of severe outlet obstruction. (radiologytoday.net)
Epidural Lipomatosis1
The patient was tentatively diagnosed with spinal epidural lipomatosis (SEL) secondary to hypothyroidism. (e-jvc.org)
ECCL4
Encephalocraniocutaneous lipomatosis (ECCL) is a rare condition that primarily affects the brain, eyes, and skin of the head and face. (medlineplus.gov)
There are no effective treatment modalities for encephalocraniocutaneous lipomatosis (ECCL). (medscape.com)
Owing to reported midline low-grade gliomas in the suprasellar region in 4 encephalocraniocutaneous lipomatosis (ECCL) patients, some authors also recommend ophthalmologic and endocrinologic control in order to quickly discover any warning signs. (medscape.com)
Grade II pilocytic astrocytoma in a 3-month-old patient with encephalocraniocutaneous lipomatosis (ECCL): case report and literature review of low grade gliomas in ECCL. (medscape.com)
Encephalocraniocutaneous24
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis. (medlineplus.gov)
[ 1 ] They suggested that the man had a previously unreported neurocutaneous syndrome, which they termed encephalocraniocutaneous lipomatosis. (medscape.com)
Encephalocraniocutaneous lipomatosis has also become known under the term Fishman syndrome. (medscape.com)
All reported cases of encephalocraniocutaneous lipomatosis are sporadic. (medscape.com)
A nonhereditary, autosomal mutation that may survive only in a mosaic state may be a cause of the clinical picture of encephalocraniocutaneous lipomatosis. (medscape.com)
In 2004, Cultrera et al described a female infant that showed significant overlap of encephalocraniocutaneous lipomatosis with oculocerebrocutaneous Delleman syndrome. (medscape.com)
Haberland C, Perou M. Encephalocraniocutaneous lipomatosis. (medscape.com)
Observations on encephalocraniocutaneous lipomatosis. (medscape.com)
Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene. (medscape.com)
Ayer RE, Zouros A. Encephalocraniocutaneous lipomatosis: a review of its clinical pathology and neurosurgical indications. (medscape.com)
Hauber K, Warmuth-Metz M, Rose C, Brocker EB, Hamm H. Encephalocraniocutaneous lipomatosis: a case with unilateral odontomas and review of the literature. (medscape.com)
Moog U. Encephalocraniocutaneous lipomatosis. (medscape.com)
Encephalocraniocutaneous lipomatosis: a rare neurocutaneous syndrome. (medscape.com)
Encephalocraniocutaneous lipomatosis with didymosis aplasticopsilolipara. (medscape.com)
Almer Z, Vishnevskia-Dai V, Zadok D. Encephalocraniocutaneous lipomatosis: case report and review of the literature. (medscape.com)
Valladares MJ, Blanco MJ, Lopez-Lopez F, Gonzalez F. Bilateral ocular involvement in encephalocraniocutaneous lipomatosis. (medscape.com)
Thakur S, Thakur V, Sood RG, Thakur CS, Khanna S. Encephalocraniocutaneous lipomatosis with calvarial exostosis - Case report and review of literature. (medscape.com)
Pregowska K, Jurkiewicz E, Miszczak-Knecht M, Turska-Kmiec A, Bieganowska K. Persistent multifocal atrial tachycardia in infant with encephalocraniocutaneous lipomatosis: a case report. (medscape.com)
Oculocerebrocutaneous and encephalocraniocutaneous lipomatosis syndromes: blind men and an elephant or separate syndromes? (medscape.com)
Brain anomalies in encephalocraniocutaneous lipomatosis. (medscape.com)
Encephalocraniocutaneous lipomatosis accompanied by the formation of bone cysts: Harboring clues to pathogenesis? (medscape.com)
Zielinska-Kazmierska B, Grodecka J, Jablonska-Polakowska L, Arkuszewski P. Mandibular osteoma in the encephalocraniocutaneous lipomatosis. (medscape.com)
Koishi GN, Yoshida M, Alonso N, Matushita H, Goldenberg D. Encephalocraniocutaneous lipomatosis (Haberland's syndrome): a case report of a neurocutaneous syndrome and a review of the literature. (medscape.com)
Lipomas6
Lipomatosis is believed to be an autosomal dominant condition in which multiple lipomas are present on the body. (wikipedia.org)
A forum and community offering information, alternative treatments, resources and support concerning lipomas, lipomatosis and other related conditions. (lipomaboard.com)
Familial multiple lipomatosis is a hereditary disorder of multiple lipomas. (doctorshealthpress.com)
The lipomas in lipomatosis cases and lipodystrophic cases were superficially located, yet they were not considered as simple and encapsulated lipomas becasue their resections were not as simple as those of the latter. (medicaljournal-ias.org)
Although it was not difficult to resect the lipomas in superficially located cases, it is believed that liposuction is not a proper treatment for the lipomas seen in the syndromic lipomatosis cases. (medicaljournal-ias.org)
Multiple lipomas may run in families and be part of a genetic condition (for example, familiar multiple lipomatosis). (msdmanuals.com)
Familial1
In my practice, I see many people with lipedema, familial multiple lipomatosis (FML), Madelung's disease and Dercum's disease (adiposis dolorosa). (tillysmidt.nl)
Symmetrical2
Multiple symmetrical lipomatosis, or Madelung's disease, is a rare disease of unknown etiology. (hindawi.com)
In other words, its was located in either the submuscular or subfascial plane.Lipomatosis was diagnosed in seven cases and lipodystrophic syndrome in five cases. (medicaljournal-ias.org)
Multiple1
Click on the microphone icon and begin speaking Lipomatosis Multiple Symmetric . (pronouncehippo.com)
Fatty1
Pancreatic lipomatosis is characterized by fatty infiltration or replacement of the pancreas, and has been associated with many conditions. (korea.ac.kr)
Diabetes1
We recently experienced two cases of pancreatic lipomatosis in patients with pancreatic pseudocyst and a case of lipomatosis in diabetes mellitus. (korea.ac.kr)
Symptoms1
When Do Symptoms of Facial infiltrating lipomatosis Begin? (nih.gov)
Cases1
In our study, we documented two unusual cases of renal replacement lipomatosis (RRL), a type of pseudotumor related to nonfunctioning kidneys. (who.int)
Patients1
In these patients, abrupt obstruction of the main pancreatic duct with smooth tapering is a typical endoscopic retrograde pancreatography (ERP) finding of pancreatic lipomatosis and must be differentiated with pancreatic carcinoma. (korea.ac.kr)
Treatment1
Treatment, with isolated lipomatosis methods a diet for lung and practices. (lorenzopetrantoni.com)
People2
This graph shows the total number of publications written about "Lipomatosis" by people in UAMS Profiles by year, and whether "Lipomatosis" was a major or minor topic of these publications. (uams.edu)
Below are the most recent publications written about "Lipomatosis" by people in Profiles over the past ten years. (uams.edu)
Development1
Development of massive lipomatosis may be caused by Adv 36. (cdc.gov)
Medical1
Lipomatosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (uams.edu)
Encephalocraniocutaneous Lipomatosis40
When Do Symptoms of Encephalocraniocutaneous lipomatosis Begin? (nih.gov)
Encephalocraniocutaneous lipomatosis (ECCL) is a rare condition that primarily affects the brain, eyes, and skin of the head and face. (medlineplus.gov)
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis. (medlineplus.gov)
Haberland C, Perou M. Encephalocraniocutaneous lipomatosis. (medscape.com)
Zielinska-Kazmierska B, Grodecka J, Jablonska-Polakowska L, Arkuszewski P. Mandibular osteoma in the encephalocraniocutaneous lipomatosis. (medscape.com)
Koishi GN, Yoshida M, Alonso N, Matushita H, Goldenberg D. Encephalocraniocutaneous lipomatosis (Haberland's syndrome): a case report of a neurocutaneous syndrome and a review of the literature. (medscape.com)
Clinical manifestation and neurosurgical intervention of encephalocraniocutaneous lipomatosis--a case report and review of the literature. (medscape.com)
Observations on encephalocraniocutaneous lipomatosis. (medscape.com)
Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene. (medscape.com)
Ayer RE, Zouros A. Encephalocraniocutaneous lipomatosis: a review of its clinical pathology and neurosurgical indications. (medscape.com)
Hauber K, Warmuth-Metz M, Rose C, Brocker EB, Hamm H. Encephalocraniocutaneous lipomatosis: a case with unilateral odontomas and review of the literature. (medscape.com)
Moog U. Encephalocraniocutaneous lipomatosis. (medscape.com)
Encephalocraniocutaneous lipomatosis: a rare neurocutaneous syndrome. (medscape.com)
Encephalocraniocutaneous lipomatosis with didymosis aplasticopsilolipara. (medscape.com)
Almer Z, Vishnevskia-Dai V, Zadok D. Encephalocraniocutaneous lipomatosis: case report and review of the literature. (medscape.com)
Encephalocraniocutaneous lipomatosis (ECCL) is a sporadically occurring neurocutaneous disorder of unknown aetiology. (nih.gov)
Encephalocraniocutaneous lipomatosis (ECCL) is a rare, congenital, neurocutaneous disorder with unilateral lipomatous cutaneous neoplasms devoid of hair and ipsilateral ophthalmologic and neurologic malformations. (medscape.com)
[ 1 ] They suggested that the man had a previously unreported neurocutaneous syndrome, which they termed encephalocraniocutaneous lipomatosis. (medscape.com)
Encephalocraniocutaneous lipomatosis has also become known under the term Fishman syndrome. (medscape.com)
All reported cases of encephalocraniocutaneous lipomatosis are sporadic. (medscape.com)
A nonhereditary, autosomal mutation that may survive only in a mosaic state may be a cause of the clinical picture of encephalocraniocutaneous lipomatosis. (medscape.com)
There are no effective treatment modalities for encephalocraniocutaneous lipomatosis (ECCL). (medscape.com)
Owing to reported midline low-grade gliomas in the suprasellar region in 4 encephalocraniocutaneous lipomatosis (ECCL) patients, some authors also recommend ophthalmologic and endocrinologic control in order to quickly discover any warning signs. (medscape.com)
In 2004, Cultrera et al described a female infant that showed significant overlap of encephalocraniocutaneous lipomatosis with oculocerebrocutaneous Delleman syndrome. (medscape.com)
Encephalocraniocutaneous lipomatosis (ECCL) comprises a spectrum of predominantly congenital anomalies. (nih.gov)
Encephalocraniocutaneous lipomatosis (ECCL) is a rare congenital syndrome with an unknown etiology. (wustl.edu)
2. Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis. (nih.gov)
3. Sensitive detection of FGFR1 N546K mosaic mutation in patient with encephalocraniocutaneous lipomatosis and pilocytic astrocytoma. (nih.gov)
7. Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis. (nih.gov)
8. Encephalocraniocutaneous Lipomatosis Without Ocular Malformations. (nih.gov)
9. Expending the Phenotypic Spectrum of Encephalocraniocutaneous Lipomatosis: About a Prenatal Case With Complete Autopsy. (nih.gov)
10. Methylome analysis and whole-exome sequencing reveal that brain tumors associated with encephalocraniocutaneous lipomatosis are midline pilocytic astrocytomas. (nih.gov)
13. Encephalocraniocutaneous lipomatosis accompanied by the formation of bone cysts: Harboring clues to pathogenesis? (nih.gov)
14. Encephalocraniocutaneous lipomatosis: a case with unilateral odontomas and review of the literature. (nih.gov)
15. Encephalocraniocutaneous lipomatosis (ECCL): neuroradiological findings in three patients and a new association with fibrous dysplasia. (nih.gov)
16. Next generation sequencing aids diagnosis and management in a case of encephalocraniocutaneous lipomatosis. (nih.gov)
17. Mosaic KRAS mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension. (nih.gov)
Connective tissue naevi are sometimes found in other diseases including tuberous sclerosis, chronic myelocytic leukaemia , syphilis and encephalocraniocutaneous lipomatosis. (dermnetnz.org)
Epidural10
Epidural lipomatosis is usually caused by idiopathic obesity or corticosteroid use. (fluoridealert.org)
Fluorosis and epidural lipomatosis are each rare causes of compressive myelopathy, and have never been described previously as a combined cause of spinal stenosis leading to myelopathy. (fluoridealert.org)
Spinal epidural lipomatosis is a rather rare condition in which the spinal canal narrows and disrupts the surrounding nerves. (asapclinics.com)
In this article, we are going to discuss epidural lipomatosis - its causes and treatment options. (asapclinics.com)
Epidural lipomatosis is a rare condition that causes a narrowing of the spinal canal and compression of the nerves in the spine. (asapclinics.com)
Epidural lipomatosis is most common in patients with obesity, steroid overproduction, or those who have undergone extensive exogenous steroid therapy. (asapclinics.com)
Treating spinal epidural lipomatosis requires, first and foremost, an accurate diagnosis of the condition. (asapclinics.com)
If you are experiencing symptoms of epidural lipomatosis, contact a Minnesota pain doctor today. (asapclinics.com)
Age, sex, body max index (BMI), hematological evaluation, blood pressure, presence of metabolic syndrome, the visceral fat area on abdominal computed tomography, and spinal epidural lipomatosis (SEL) on magnetic resonance imaging were evaluated. (elsevierpure.com)
Liposis1
Lipomatosis is also referred to as: liposis or adiposis. (davinciplastic.com)
Autosomal1
Lipomatosis is believed to be an autosomal dominant condition in which multiple lipomas are present on the body. (wikipedia.org)
However, with age, the normal tissue in the lymph nodes (called "the stroma") is gradually replaced by adipose tissue (fat), in a phenomenon known as lipomatosis. (earth.com)
Disease1
Pelvic lipomatosis - A rare disease most often seen in older obese black men with hypertension. (wikipedia.org)
Term1
Our study is a first step towards understanding why lipomatosis occur, and towards the longer term goal of finding ways to prevent its progression and the destruction of the lymph node," said study lead author Tove Bekkhus, an expert in Immunology, Genetics, and Pathology at Uppsala. (earth.com)