ABSTRACT
Papuloerythroderma of Ofuji (1) is a rare intensely pruritic erythrodermic dermatosis with a polymorphous etiology which frequently includes an association with CTCL, visceral malignancy or immunodeficiency. Since papuloerythroderma has differential diagnostic implications in the context of malignant lymphoma, it is briefly discussed here. It is not listed in any of the major lymphoma classifications.
