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Lipedema, a Rare Disease

Identifieur interne : 004E23 ( Main/Merge ); précédent : 004E22; suivant : 004E24

Lipedema, a Rare Disease

Auteurs : Bae Wook Shin [Corée du Sud] ; Young-Joo Sim [Corée du Sud] ; Ho Joong Jeong [Corée du Sud] ; Ghi Chan Kim [Corée du Sud]

Source :

Annals of Rehabilitation Medicine [ 2234-0645 ] ; 2011.

RBID : PMC:3309375

Abstract

Lipedema is a chronic disease of lipid metabolism that results in the symmetrical impairment of fatty tissue distribution and storage combined with the hyperplasia of individual fat cells. Lipedema occurs almost exclusively in women and is usually associated with a family history and characteristic features. It can be diagnosed based on clinical history and physical examination. Lipedema is usually symmetrical, but spares the feet, is often painful to palpation, and is negative for Stemmer's sign. Additionally, lipedema patients can present with microangiopathies and lipomas. The well-known therapies for lipedema include complex decongestive therapy, pneumatic compression, and diet modifications. However, whether these treatments help reduce swelling is debatable. We encountered a case of lipedema that was initially misdiagnosed as lymphedema. The patient's clinical features and history were different from those typical of lymphedema, prompting a diagnosis of lipedema and she was treated with a complex decongestive therapy program.

Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3309375

DOI: 10.5535/arm.2011.35.6.922
PubMed: 22506222
PubMed Central: 3309375

Links to Exploration step

PMC:3309375

Le document en format XML

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Serveur d'exploration sur le lymphœdème

Lipedema, a Rare Disease

Lipedema, a Rare Disease

Source :

Abstract

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Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki

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