A Comprehensive Case Report on Familial Multiple Lipomatosis

A Comprehensive Case Report on Familial Multiple Lipomatosis

ABSTRACT Familial multiple lipomatosis (FML) is a rare autosomal dominant disorder characterized by the progressive development of encapsulated nodules predominantly on the trunk and extremities. Its genetic basis is linked to HMGA‐2 gene over‐expression. The condition is diagnosed via clinical hist...

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Bibliographic Details
Main Authors: Fatima Ali Raza, Syed Abdullah Monawwer, Muhammad Husnain, Darja Golubeva, Laveeza Fatima, Md Ariful Haque
Format: Article
Language:English
Published: Wiley 2024-12-01
Series:Clinical Case Reports
Subjects:
autosomal dominant disorder
familial multiple lipomatosis
FML
HMGA‐2 gene
Online Access:https://doi.org/10.1002/ccr3.9664
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Summary:ABSTRACT Familial multiple lipomatosis (FML) is a rare autosomal dominant disorder characterized by the progressive development of encapsulated nodules predominantly on the trunk and extremities. Its genetic basis is linked to HMGA‐2 gene over‐expression. The condition is diagnosed via clinical history, ultrasound findings, and histological studies, and management mainly comprises surgical excision. This case report highlights the clinical characteristics, diagnostic challenges, and management of FML in a 38‐year‐old male.
ISSN:2050-0904

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