Ofuji papuloerythrodema is a rare type of dermatosis marked by an erythrode
rmic manifestation which is intensely pruritic and results from the coalesc
ing of brownish papules which in the main do not involve the great folds. T
he authors present the case history of a 72-year-old female, whose dermatos
is appeared 8 years after the diagnosis of malignant lymphocitic lymphoma.
The Authors describe the clinical and histopathological picture, illustrati
ng the laboratory results and stressing the importance of the association o
f the two pathologies in a possible nosological overview.