Cargando…
Isolated Congenital Lower Limb Lipoatrophy: A Case Report and Literature Review
Lipoatrophy and lipodystrophy can often be used interchangeably in the literature. However, there are some key differences. Inflammation plays a preliminary role in subcutaneous adipose tissue (SAT) loss in lipoatrophy, whereas lipodystrophy does not. There are acquired causes of SAT loss such as in...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465101/ https://www.ncbi.nlm.nih.gov/pubmed/37650095 http://dx.doi.org/10.1097/GOX.0000000000005222 |
_version_ | 1785098603104043008 |
---|---|
author | Alhusain, Abdullah M. Alrodiman, Osama A. Alfaqeeh, Faisal A. Alissa, Sami I. |
author_facet | Alhusain, Abdullah M. Alrodiman, Osama A. Alfaqeeh, Faisal A. Alissa, Sami I. |
author_sort | Alhusain, Abdullah M. |
collection | PubMed |
description | Lipoatrophy and lipodystrophy can often be used interchangeably in the literature. However, there are some key differences. Inflammation plays a preliminary role in subcutaneous adipose tissue (SAT) loss in lipoatrophy, whereas lipodystrophy does not. There are acquired causes of SAT loss such as injurious stimuli (ie, drug injections), panniculitis, or even microtrauma. Moreover, there are congenital causes such as familial partial lipodystrophy, which follows a more localized pathology, and congenital generalized lipodystrophy, which follow a diffuse spread of SAT loss. These etiologies are further subdivided based on the mutations and clinical presentations. We present a case of a 12-year-old girl with unilateral left lower limb SAT loss since birth, without any signs of inflammation. Therefore, a diagnosis of familial partial lipodystrophy was suspected. However, genetic testing appeared unremarkable. The patient is set for conservative therapy until late adolescence for possible fat grafting. |
format | Online Article Text |
id | pubmed-10465101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-104651012023-08-30 Isolated Congenital Lower Limb Lipoatrophy: A Case Report and Literature Review Alhusain, Abdullah M. Alrodiman, Osama A. Alfaqeeh, Faisal A. Alissa, Sami I. Plast Reconstr Surg Glob Open Reconstructive Lipoatrophy and lipodystrophy can often be used interchangeably in the literature. However, there are some key differences. Inflammation plays a preliminary role in subcutaneous adipose tissue (SAT) loss in lipoatrophy, whereas lipodystrophy does not. There are acquired causes of SAT loss such as injurious stimuli (ie, drug injections), panniculitis, or even microtrauma. Moreover, there are congenital causes such as familial partial lipodystrophy, which follows a more localized pathology, and congenital generalized lipodystrophy, which follow a diffuse spread of SAT loss. These etiologies are further subdivided based on the mutations and clinical presentations. We present a case of a 12-year-old girl with unilateral left lower limb SAT loss since birth, without any signs of inflammation. Therefore, a diagnosis of familial partial lipodystrophy was suspected. However, genetic testing appeared unremarkable. The patient is set for conservative therapy until late adolescence for possible fat grafting. Lippincott Williams & Wilkins 2023-08-29 /pmc/articles/PMC10465101/ /pubmed/37650095 http://dx.doi.org/10.1097/GOX.0000000000005222 Text en Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Reconstructive Alhusain, Abdullah M. Alrodiman, Osama A. Alfaqeeh, Faisal A. Alissa, Sami I. Isolated Congenital Lower Limb Lipoatrophy: A Case Report and Literature Review |
title | Isolated Congenital Lower Limb Lipoatrophy: A Case Report and Literature Review |
title_full | Isolated Congenital Lower Limb Lipoatrophy: A Case Report and Literature Review |
title_fullStr | Isolated Congenital Lower Limb Lipoatrophy: A Case Report and Literature Review |
title_full_unstemmed | Isolated Congenital Lower Limb Lipoatrophy: A Case Report and Literature Review |
title_short | Isolated Congenital Lower Limb Lipoatrophy: A Case Report and Literature Review |
title_sort | isolated congenital lower limb lipoatrophy: a case report and literature review |
topic | Reconstructive |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465101/ https://www.ncbi.nlm.nih.gov/pubmed/37650095 http://dx.doi.org/10.1097/GOX.0000000000005222 |
work_keys_str_mv | AT alhusainabdullahm isolatedcongenitallowerlimblipoatrophyacasereportandliteraturereview AT alrodimanosamaa isolatedcongenitallowerlimblipoatrophyacasereportandliteraturereview AT alfaqeehfaisala isolatedcongenitallowerlimblipoatrophyacasereportandliteraturereview AT alissasamii isolatedcongenitallowerlimblipoatrophyacasereportandliteraturereview |