PAPULAR MUCINOSIS (SCLEROMYXOEDEMA) COMPLICATING DIFFUSE SYSTEMIC SCLEROSIS: CLINICAL FEATURES AND ELECTRON MICROSCOPE OBSERVATIONS

János Varga, Lois Y. Matsuoka, Ken Hashimoto, M. di Leonardo, Sergio A. Jiménez

Lara D. Veeken · 1992 · 12 citations · 0 references

Concepts

Abstract

Papular mucinosis (scleromyxoedema) is an uncommon disorder characterized by generalized papular eruption and cutaneous induration, which may be associated with a variety of extracutaneous manifestations. Although scleroderma and papular mucinosis share many features, they are clinically and histologically distinct entities. We report here a patient with diffuse scleroderma who developed superimposed papular mucinosis. Degranulating mast cells were a prominent ultrastructural finding in the involved skin. The occurrence of scleroderma and papular mucinosis, two uncommon cutaneous indurative diseases, in the same patient has not been described previously.