Cutaneous Rosai-Dorfman Disease

被引：4

作者：

Gaul, Maren ^{[1
,2
]}

Chang, Timothy ^{[3
]}

机构：

[1] Western Reserve Hosp, Cuyahoga Falls, OH USA

[2] Tanana Valley Clin, Fairbanks, AK USA

[3] Case Western Reserve Univ, Sch Med, Beachwood, OH USA

来源：

CUTIS | 2019年 / 103卷 / 03期

关键词：

IMATINIB;

D O I：

暂无

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Cutaneous Rosai-Dorfman disease (CRDD) is a rare form of Rosai-Dorfman disease (RDD)(also known as sinus histiocytosis with massive lymphadenopathy) that has a varied clinical presentation, an unknown etiology, and multiple treatment options that lack efficacy. We present a case of a 31-year-old woman who presented with grouped flesh-colored to light pink papules and plaques within a hyperpigmented patch on the thigh that were treated with topical, oral, and intralesional steroids with minimal improvement.

引用

页码：171 / 173

页数：3

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