Mucha-Habermann Disease: The Quandary Continues

Q4 Medicine

Journal, Indian Academy of Clinical Medicine Pub Date : 2022-06-01 DOI:10.1177/26339447221123393

L. Mezni, Farah Elhadadi, M. Meziane, N. Ismaili, L. Benzekri, K. Senouci

引用次数: 0

Abstract

Pityriasis lichenoides et varioliformis acuta (PLEVA) is an uncommon skin disorder, clinically characterized by an acute onset of a polymorphic eruption. The disease has an unpredictable course, the pathogenesis is not fully understood, and many treatments have been proposed while self-resolution may occur. Hence, We report a puzzling case of PLEVA in its early stage of transition to a febrile ulceronecrotic Mucha-Habermann disease.

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穆夏-哈伯曼病:困境仍在继续

急性地衣样变糠疹(PLEVA)是一种罕见的皮肤病，临床特征是急性发作的多形态疹。这种疾病的病程不可预测，发病机制尚不完全清楚，许多治疗方法已经提出，但可能会发生自我解决。因此，我们报告一个令人困惑的PLEVA在其早期阶段过渡到发热溃疡性Mucha-Habermann病。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Journal, Indian Academy of Clinical Medicine Medicine-Medicine (all)

CiteScore

0.10

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0.00%

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期刊介绍： Indian Association of Clinical Medicine is an academic body constituted in the year 1992 by a group of clinicians with the main aim of reaffirming the importance of clinical medicine in this era of high-tech diagnostic modalities. There is no doubt that modern investigational methods have contributed a lot to the present day medical practice but that does not render clinical acumen and examination less important. The art and science of clinical medicine helps up to make proper and judicious use of investigations and not these be the sole basis of our practice. That is the basic idea behind this ''Association''. We presently have members and fellows of the association from all over the country. In August, 2002 the body was registered as "Indian Association of Clinical Medicine" by the Registrar of Societies, Delhi.