A Case of Pemphigus Herpetiformis in a 12-Year-Old Male
Author(s) -
O. Hocar,
Imane Ait Sab,
N. Akhdari,
M Hakkou,
S. Amal
Publication year - 2011
Publication title -
isrn pediatrics
Language(s) - English
Resource type - Journals
eISSN - 2090-4703
pISSN - 2090-469X
DOI - 10.5402/2011/712560
Subject(s) - dermatitis herpetiformis , pemphigus , medicine , dermatology , acantholysis , bulla (seal) , dapsone , spongiosis , direct fluorescent antibody , pathology , prednisone , autoantibody , antibody , gastroenterology , disease , immunology , lung
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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom