A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations

Shintaro Saito MD, Akihiko Uchiyama MD, PhD, Yayoi Shibusawa MD, PhD, Sei-ichiro Motegi MD, PhD
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引用次数: 0

Abstract

Rosai–Dorfman disease (RDD) is a rare non-Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969. While classical/nodal RDD is typical, extranodal involvement is seen in up to 43% of all cases, with 23% showing only extranodal lesions. Here, we present a case of disseminated extranodal RDD, where the initial symptoms were cutaneous manifestations.

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皮肤表现诊断为弥漫性结外Rosai–Dorfman病1例
Rosai - Dorfman病(RDD)是一种罕见的非朗格汉斯细胞性组织细胞增多症,于1969年由Rosai和Dorfman首次描述为窦性组织细胞增多症伴大量淋巴结病。虽然经典/淋巴结性RDD是典型的,但高达43%的病例可见到结外病变,其中23%仅表现为结外病变。在此,我们报告一例播散性结外RDD,其初始症状为皮肤表现。
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来源期刊
CiteScore
0.60
自引率
10.00%
发文量
69
审稿时长
12 weeks
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