科研之友
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摘要
pityriasis lichenoides is a rare idiopathic cutaneous disorder, with a clinical-histopathological spectrum comprising the acute varioliform form (mucha-habermann%26apos;s disease), its febrile ulceronecrotic variant, and its chronic form. systemic manifestations may occur in the febrile ulceronecrotic variant, with reports of adult mortality. the case of a young male patient with clinical and histopathological diagnosis of mucha-habermann＊s disease, febrile ulceronecrotic variant, with severe mucosal involvement - an occasional incidence even in the most severe forms of pityriasis lichenoides - is presented. in addition to the atypical clinical aspect, an excellent therapeutic result is shown with the association of prednisone and methotrexate.
