Korean J Dermatol.  2002 Feb;40(2):158-161.

A Case of Papuloerythroderma of Ofuji

Affiliations
  • 1Department of Dermatology, College of Medicine, The Catholic University of Korea, Seoul, Korea. OSTKSY@cmc.cuk.ac.kr

Abstract

Papuloerythroderma of Ofuji is a rare, distinctive clinical entity characterized by a widespread pruritic eruption of coalescence of flat-topped erythematous papules producing an erythroderma with sparing of the skin folds (the 'deck-chair' sign). Other common features of papuloerythroderma are blood eosinophilia, lymphopenia, a raised serum IgE and a nonspecific or eczematous-like histopathologic feature. Its etiology has been reported as variable, and the condition is thus considered as a pattern of cutaneous expression induced by a range of pathological process for systemic disease. We experienced a 71-year-old male patient with a 4-month history of a generalized pruritic eruption which clinical features were compatible with papuloerythroderma of Ofuji. Treatment with systemic steroid resulted in marked improvement.

Keyword

Papuloerythroderma

MeSH Terms

Aged
Dermatitis, Exfoliative
Eosinophilia
Humans
Immunoglobulin E
Lymphopenia
Male
Skin
Immunoglobulin E
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