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A case of pemphigus herpetiformis in a 12-year-old male.

作者信息

Hocar O, Ait Sab I, Akhdari N, Hakkou M, Amal S

机构信息

Dermatology Department, School of Medicine, Cadi Ayyad University, Mohammed the VIth University Hospital Marrakesh, Morocco.

出版信息

ISRN Pediatr. 2011;2011:712560. doi: 10.5402/2011/712560. Epub 2011 Apr 7.

Abstract

Pemphigus herpetiformis (PH) is one of the less common forms of pemphigus. PH in children is unreported. We describe a case of a child who developed PH. Observation. A 12-year-old boy was seen at our department with erosive plaques, vesicles, and crusted cutaneous lesions associated with severe itching persisting for six months. Histologic examination showed an intraepidermal bulla containing rare acantholytic epidermal cells with eosinophilic spongiosis. Direct immunofluorescence demonstrated intercellular Ig G and C3 deposit. The serum titer of antibodies against intercellular epidermal was 1/200 UI/l. Diagnosis of PH was made, and treatment with Dapsone 2 mg/kg per day resulted in total clinical remission. However, two months later, new vesicles reappeared and treatment was begun with prednisone at a dose of 2 mg/kg daily. There was a very good response. Discussion. Childhood pemphigus herpetiformis is a rare disease, often initially misdiagnosed. It must not be forgotten that the disease is a possible cause of erosive mucocutaneous disease in children.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a407/3263577/c66a041fa4ab/PEDIATRICS2011-712560.001.jpg

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