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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| Format: | Article |
| Language: | English |
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Wiley
2024-12-01
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| Series: | Clinical Case Reports |
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| Online Access: | https://doi.org/10.1002/ccr3.9664 |
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| author | Fatima Ali Raza Syed Abdullah Monawwer Muhammad Husnain Darja Golubeva Laveeza Fatima Md Ariful Haque |
| author_facet | Fatima Ali Raza Syed Abdullah Monawwer Muhammad Husnain Darja Golubeva Laveeza Fatima Md Ariful Haque |
| author_sort | Fatima Ali Raza |
| collection | DOAJ |
| description | 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. |
| format | Article |
| id | doaj-art-75afe51cfa32474c86a79d5bf2cc43a3 |
| institution | Kabale University |
| issn | 2050-0904 |
| language | English |
| publishDate | 2024-12-01 |
| publisher | Wiley |
| record_format | Article |
| series | Clinical Case Reports |
| spelling | doaj-art-75afe51cfa32474c86a79d5bf2cc43a32024-12-26T06:30:42ZengWileyClinical Case Reports2050-09042024-12-011212n/an/a10.1002/ccr3.9664A Comprehensive Case Report on Familial Multiple LipomatosisFatima Ali Raza0Syed Abdullah Monawwer1Muhammad Husnain2Darja Golubeva3Laveeza Fatima4Md Ariful Haque5Karachi Medical and Dental College Karachi PakistanZiauddin Medical University Karachi PakistanNishtar Medical University and Hospital Multan PakistanRiga Stradins University Riga LatviaAllama Iqbal Medical College Lahore PakistanDepartment of Public Health Atish Dipankar University of Science and Technology Dhaka BangladeshABSTRACT 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.https://doi.org/10.1002/ccr3.9664autosomal dominant disorderfamilial multiple lipomatosisFMLHMGA‐2 gene |
| spellingShingle | Fatima Ali Raza Syed Abdullah Monawwer Muhammad Husnain Darja Golubeva Laveeza Fatima Md Ariful Haque A Comprehensive Case Report on Familial Multiple Lipomatosis Clinical Case Reports autosomal dominant disorder familial multiple lipomatosis FML HMGA‐2 gene |
| title | A Comprehensive Case Report on Familial Multiple Lipomatosis |
| title_full | A Comprehensive Case Report on Familial Multiple Lipomatosis |
| title_fullStr | A Comprehensive Case Report on Familial Multiple Lipomatosis |
| title_full_unstemmed | A Comprehensive Case Report on Familial Multiple Lipomatosis |
| title_short | A Comprehensive Case Report on Familial Multiple Lipomatosis |
| title_sort | comprehensive case report on familial multiple lipomatosis |
| topic | autosomal dominant disorder familial multiple lipomatosis FML HMGA‐2 gene |
| url | https://doi.org/10.1002/ccr3.9664 |
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