Potts Christopher A, Bozeman Andrew P, Walker Anna N, Floyd Waldo E
Departments of Surgery (Hand) and Pathology, Mercer University School of Medicine, Macon, GA 31207, USA.
J Hand Surg Am. 2008 Oct;33(8):1409-13. doi: 10.1016/j.jhsa.2008.04.003.
Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease (RDD), is a rare non-neoplastic pathologic condition that frequently pursues a prolonged clinical course marked by exacerbations and remissions. Cutaneous RDD is even less common than cases involving lymph nodes. We present the case of a patient with long-standing Crohn's disease who developed cutaneous RDD in the forearm.
伴巨大淋巴结病的窦组织细胞增生症,也称为罗萨伊-多夫曼病(RDD),是一种罕见的非肿瘤性病理状况,其临床病程通常较长,有病情加重和缓解的情况。皮肤型RDD比累及淋巴结的病例更为少见。我们报告一例患有长期克罗恩病的患者,其前臂出现了皮肤型RDD。