Lu Li-yan, Ju Wu-tong, Cai Ming, Lu Xiao-feng
Department of Oral and Maxillofacial Surgery, Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai Key Laboratory of Stomatology, Shanghai, China.
J Craniofac Surg. 2012 Sep;23(5):e509-10. doi: 10.1097/SCS.0b013e318266fb64.
Rosai-Dorfman disease (RDD), also named sinus histiocytosis with massive lymphadenopathy, is a rare, idiopathic, and benign disorder that classically presents as a painless massive bilateral cervical lymphadenopathy. In cases of extranodal presentations, such as cutaneous RDD, it may not involve the classic manifestation. The diagnosis is usually made by histopathologic analysis. Surgery is suggested in the cases of significant cosmetic deformity or when there is fatal or functional obstruction. We reported a case of extranodal RDD that recurred in the infraorbital region postoperatively.
罗萨伊-多夫曼病(RDD),也称为伴有巨大淋巴结病的窦性组织细胞增多症,是一种罕见的、特发性的良性疾病,典型表现为无痛性双侧颈部巨大淋巴结病。在结外表现的病例中,如皮肤型RDD,可能不涉及经典表现。诊断通常通过组织病理学分析做出。在存在明显美容畸形或有致命性或功能性梗阻的情况下建议进行手术。我们报告了1例结外RDD病例,该病例术后在眶下区域复发。