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A Comprehensive Case Report on Familial Multiple Lipomatosis.
Fatima Ali Raza1, Syed Abdullah Monawwer2, Muhammad Husnain3
1Karachi Medical and Dental College Karachi Pakistan.
Clinical Case Reports
|December 2, 2024
Summary
Familial multiple lipomatosis (FML) is a rare genetic disorder causing numerous lipomas. This case report details the clinical presentation, diagnosis, and surgical management of a 38-year-old male patient.
Area of Science:
- Genetics
- Dermatology
- Oncology
Background:
- Familial multiple lipomatosis (FML) is an autosomal dominant disorder.
- Characterized by progressive development of encapsulated nodules on trunk and extremities.
- Genetic basis linked to HMGA-2 gene over-expression.
Purpose of the Study:
- To highlight clinical characteristics of FML.
- To discuss diagnostic challenges in FML.
- To present management strategies for FML.
Main Methods:
- Clinical history review.
- Ultrasound imaging.
- Histological examination.
Main Results:
- Progressive development of encapsulated lipomas.
- Diagnosis confirmed via clinical, ultrasound, and histological findings.
- Management primarily involved surgical excision.
Conclusions:
- FML presents with characteristic lipoma development.
- Multimodal diagnostic approach is crucial for FML.
- Surgical excision remains the primary treatment for FML.
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