Engelures

A.-M. Sarteel-Delvoye , T. Wiart , A. Legrand
{"title":"Engelures","authors":"A.-M. Sarteel-Delvoye ,&nbsp;T. Wiart ,&nbsp;A. Legrand","doi":"10.1016/j.emcaa.2005.07.012","DOIUrl":null,"url":null,"abstract":"<div><p>Chilblain is an erytrocyanosis lesion of the lower limb extremities, associated with pruritus and scraping when warming. This disorder is characterized by its occurrence after exposure to moderate damp cold, its regression in 2 or 3 weeks, and relapses during wintertime. More often it concerns slim young women, but can be seen at all ages, even in older men. Clinic appearance greatly varies. In 50% of the cases, mother heredity is observed; acroyanosis occurs in 45%, and Raynaud's disease in 32% of the cases. Chilblain is benign in 60% of the patients, disabling in 34%, and ulcerate in 7%. The biological, paraclinical investigations, the main differential diagnosis, the lupus erythematosus, and the therapeutic management are reviewed, according to the disease severity.</p></div>","PeriodicalId":100413,"journal":{"name":"EMC - Cardiologie-Angéiologie","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2005-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.emcaa.2005.07.012","citationCount":"0","resultStr":"{\"title\":\"Engelures\",\"authors\":\"A.-M. Sarteel-Delvoye ,&nbsp;T. Wiart ,&nbsp;A. Legrand\",\"doi\":\"10.1016/j.emcaa.2005.07.012\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Chilblain is an erytrocyanosis lesion of the lower limb extremities, associated with pruritus and scraping when warming. This disorder is characterized by its occurrence after exposure to moderate damp cold, its regression in 2 or 3 weeks, and relapses during wintertime. More often it concerns slim young women, but can be seen at all ages, even in older men. Clinic appearance greatly varies. In 50% of the cases, mother heredity is observed; acroyanosis occurs in 45%, and Raynaud's disease in 32% of the cases. Chilblain is benign in 60% of the patients, disabling in 34%, and ulcerate in 7%. The biological, paraclinical investigations, the main differential diagnosis, the lupus erythematosus, and the therapeutic management are reviewed, according to the disease severity.</p></div>\",\"PeriodicalId\":100413,\"journal\":{\"name\":\"EMC - Cardiologie-Angéiologie\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.emcaa.2005.07.012\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EMC - Cardiologie-Angéiologie\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1762613705000163\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EMC - Cardiologie-Angéiologie","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1762613705000163","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

冻疮是下肢的一种紫绀病,在加温时伴有瘙痒和刮擦。这种病症的特点是在暴露于中度湿冷后发生,在2或3周内消退,并在冬季复发。更常见的是,它涉及苗条的年轻女性,但在所有年龄段都可以看到,甚至在年长男性身上也可以看到。临床表现千差万别。在50%的病例中,观察到母亲遗传;肢端炎发生率为45%,雷诺病发生率为32%。冻疮60%为良性,34%为致残,7%为溃疡。根据疾病的严重程度,综述了生物学、临床旁研究、主要鉴别诊断、红斑狼疮和治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engelures

Chilblain is an erytrocyanosis lesion of the lower limb extremities, associated with pruritus and scraping when warming. This disorder is characterized by its occurrence after exposure to moderate damp cold, its regression in 2 or 3 weeks, and relapses during wintertime. More often it concerns slim young women, but can be seen at all ages, even in older men. Clinic appearance greatly varies. In 50% of the cases, mother heredity is observed; acroyanosis occurs in 45%, and Raynaud's disease in 32% of the cases. Chilblain is benign in 60% of the patients, disabling in 34%, and ulcerate in 7%. The biological, paraclinical investigations, the main differential diagnosis, the lupus erythematosus, and the therapeutic management are reviewed, according to the disease severity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信