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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Papular mucinosis (scleromyxoedema) complicating diffuse systemic sclerosis: clinical features and electron
J Varga1, L Y Matsuoka, K Hashimoto
1Department of Medicine, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107.
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.

