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Papular mucinosis (scleromyxoedema) complicating diffuse systemic sclerosis: clinical features and electron microscope observations.

作者信息

Varga J, Matsuoka L Y, Hashimoto K, Di Leonardo M, Jimenez S A

机构信息

Department of Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107.

出版信息

Br J Rheumatol. 1992 Nov;31(11):779-82. doi: 10.1093/rheumatology/31.11.779.

DOI:10.1093/rheumatology/31.11.779
PMID:1450804
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.

摘要

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