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A case of febrile ulceronecrotic Mucha-Habermann disease with comorbidities

机译:高热合并大肠溃疡性Mucha-Habermann病1例

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Febrile ulceronecrotic Mucha-Habermann disease is a very rare and severe variant of pityriasis lichenoides et varioliformis acuta. Adult cases are difficult to diagnose as in the early course they can mimic erythema multiforme or lymphomatoid papulosis. We report a case of a 38-year-old woman who presented with 90% body surface area involvement, fever, diarrhea, malaise and associated comorbidities. She was treated with systemic steroids and methotrexate but suffered a fatal outcome. So far, a total of 65 cases are reported in the literature.
机译:发热性坏死性Mucha-Habermann病是糠疹性糠疹的一种非常罕见和严重的变种。成年病例很难诊断,因为它们可以模仿多形性红斑或淋巴瘤样丘疹。我们报道了一例38岁的女性,该女性呈现出90%的身体表面积受累,发烧,腹泻,全身不适和相关合并症。她接受了全身性类固醇和甲氨蝶呤治疗,但结果致命。迄今为止,文献中总共报告了65例。

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