Primary Rosai-Dorfman Disease of Bone: A Report of Two Cases.

Case Reports in Radiology Pub Date : 2019-01-03 eCollection Date: 2019-01-01 DOI:10.1155/2019/1720131
Andrew B Ross, Kirkland W Davis, Darya Buehler, Brian Y Chan
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引用次数: 8

Abstract

Rosai-Dorfman disease (RDD), sometimes known as sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic disorder that most commonly presents as painless, massive cervical lymphadenopathy in young adults. Extranodal disease can occur in up to 40% of patients but primary involvement of bone is rare. We present two cases of primary RDD of bone: one case of multifocal osseous RDD presenting as a painful lesion in the elbow, and one case of a solitary osseous lesion presenting as a painful lesion in the wrist.

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原发性骨Rosai-Dorfman病2例报告
rossai - dorfman病(RDD),有时被称为窦性组织细胞增生伴大量淋巴结病,是一种罕见的组织细胞疾病,最常见于年轻人的无痛性、大量颈部淋巴结病。结外病变可发生在高达40%的患者,但主要累及骨是罕见的。我们报告了两例原发性骨RDD:一例多灶性骨性RDD表现为肘部疼痛病变,一例孤立性骨性病变表现为手腕疼痛病变。
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