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一例发热性溃疡性坏死性蕈样肉芽肿病,对全身皮质类固醇激素治疗有反应。

A case of febrile ulceronecrotic Mucha-Habermann disease responsive to systemic corticosteroids.

机构信息

Department of Pediatrics, David Geffen School of Medicine at University of California Los Angeles, UCLA, Los Angeles, California, USA.

Division of Dermatology, David Geffen School of Medicine at University of California Los Angeles, UCLA, Los Angeles, California, USA.

出版信息

Pediatr Dermatol. 2023 May-Jun;40(3):573-575. doi: 10.1111/pde.15234. Epub 2022 Dec 27.

Abstract

Febrile ulceronecrotic Mucha-Habermann disease (FUMHD) is a rare, potentially fatal subtype of pityriasis lichenoides et varioliformis acuta (PLEVA). Herein, we present a rare case of a 14-year-old male without significant past medical history who was diagnosed with FUMHD without a clear inciting factor. He was effectively treated with systemic corticosteroids with complete resolution of symptoms.

摘要

发热性溃疡性坏死性蕈样肉芽肿病(FUMHD)是一种罕见的、潜在致命的类卟啉病样和痘疮样急性发疹性疾病(PLEVA)亚型。本文报道了一例罕见的无明显既往病史的 14 岁男性病例,该患者无明确诱发因素,被诊断为 FUMHD。他接受全身皮质类固醇治疗,症状完全缓解。

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