骨原发性罗萨伊-多夫曼病：两例报告
Primary Rosai-Dorfman Disease of Bone: A Report of Two Cases.
作者信息
Ross Andrew B, Davis Kirkland W, Buehler Darya, Chan Brian Y
机构信息
Department of Radiology, University of Wisconsin School of Medicine and Public Health, 600 Highland Ave. MC 3252, Clinical Science Center, Madison, WI 53792, USA.
Department of Radiology, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
出版信息
Case Rep Radiol. 2019 Jan 3;2019:1720131. doi: 10.1155/2019/1720131. eCollection 2019.
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.
罗萨伊-多夫曼病（RDD），有时也称为伴有巨大淋巴结病的窦性组织细胞增生症，是一种罕见的组织细胞疾病，最常见于年轻成年人，表现为无痛性、巨大的颈部淋巴结病。结外病变可发生在高达40%的患者中，但骨骼的原发性受累很少见。我们报告两例骨骼原发性RDD：一例多灶性骨RDD表现为肘部疼痛性病变，另一例孤立性骨病变表现为腕部疼痛性病变。
Zotero 插件