Mucha-Habermann Disease: The Quandary Continues

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 ma...

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Veröffentlicht in:Indian journal of clinical medicine 2022-06, Vol.12 (1-2), p.42-44
Hauptverfasser: Mezni, Line, Elhadadi, Farah, Meziane, Mariame, Ismaili, Nadia, Benzekri, Laila, Senouci, Karima
Format: Artikel
Sprache:eng
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Zusammenfassung: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.
ISSN:2633-9447
1179-9161
DOI:10.1177/26339447221123393