Scleromyxedema: An Atypical Case

被引：4

作者：

Thomas, Emy ^{[1
]}

George, Anisha ^{[1
]}

Deodhar, Divya ^{[2
]}

John, Mary ^{[2
]}

机构：

[1] Christian Med Coll & Hosp, Dept Dermatol, Ludhiana 141008, Punjab, India

[2] Christian Med Coll & Hosp, Dept Med, Ludhiana, Punjab, India

来源：

INDIAN JOURNAL OF DERMATOLOGY | 2015年 / 60卷 / 03期

关键词：

Eosinophilia; papular mucinosis; scleromyxedema; PAPULAR MUCINOSIS;

D O I：

10.4103/0019-5154.156456

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Scleromyxedema is a rare, chronic and persistent idiopathic disorder characterized by a generalized papular eruption due to dermal mucin deposition with an increase in dermal collagen. Patients usually have associated paraproteinemia. We describe the case of a 59-year-old gentleman with features of scleromyxedema, who had severe pruritus, scalp involvement, unrestricted mobility and associated peripheral eosinophilia, but no monoclonal gammopathy.

引用

页数：3

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