Mansoori Jasmin, Fisher Olivia, Akinyeye Ivana O, Sobolevsky Michael A, Quinn Robert H
Department of Orthopaedics, UT Health San Antonio, San Antonio, TX, USA.
Department of Pathology and Laboratory Medicine, UT Health San Antonio, San Antonio, TX, USA.
Foot Ankle Orthop. 2021 Dec 8;6(4):24730114211060058. doi: 10.1177/24730114211060058. eCollection 2021 Oct.
Rosai-Dorfman disease (RDD), otherwise known as sinus histiocytosis with massive lymphadenopathy (SHML), is a very rare and typically benign disorder of unknown etiology with <10% bone involvement. The report is of a case seen at the authors' hospital of a patient presenting with several months' onset unspecified nontraumatic ankle pain. There was no physical mass or lymphadenopathy appreciated on examination. Plain radiographs and magnetic resonance images demonstrated an osteolytic lesion at the medial malleolus. Biopsy revealed the diagnosis of intraosseous manifestation of Rosai-Dorfman disease.
罗萨伊-多夫曼病（RDD），又称伴有巨大淋巴结病的窦性组织细胞增生症（SHML），是一种非常罕见且通常为良性的疾病，病因不明，骨受累情况<10%。本文报告了作者所在医院收治的一例患者，该患者出现数月未明确病因的非创伤性踝关节疼痛。体格检查未发现肿物或淋巴结肿大。X线平片和磁共振成像显示内踝有溶骨性病变。活检确诊为罗萨伊-多夫曼病的骨内表现。
