John Stanley, Goel Tanubha
Department of Otorhinolaryngology, Dr. B R Ambedkar Medical College and Hospital, Kadugondanahalli, Bangalore, Karnataka 560045 India.
Indian J Otolaryngol Head Neck Surg. 2024 Feb;76(1):1260-1263. doi: 10.1007/s12070-023-04254-7. Epub 2023 Oct 11.
Rosai-Dorfman disease (RDD) is a rare histiocytic proliferative disorder of unknown etiology. Usually it presents with massive painless cervical lymph node enlargement. Histologically, it shows proliferation of distinctive histiocytic cells that demonstrate emperipolesis in the background of a mixed inflammatory infiltrates. Immunohistochemically, the cells are positive for markers such as CD68 and S100. A 14-year-old boy presented with painless right sided cervical lymphadenopathy without any systemic and other ear, nose, and throat manifestations. The biopsy report of the lymph node showed infiltration of sheets of histiocytes showing emperipolesis with areas of fibrosis and hyalinisation. The sinus histiocytes were strongly positive for S-100 protein. RDD must be considered in the differential diagnosis of massive or multiple lymphadenopathies.
罗萨伊-多夫曼病(RDD)是一种病因不明的罕见组织细胞增生性疾病。通常表现为颈部淋巴结无痛性肿大。组织学上,它显示出独特的组织细胞增生,这些细胞在混合性炎症浸润背景下呈现吞噬现象。免疫组织化学检查显示,这些细胞对CD68和S100等标志物呈阳性。一名14岁男孩出现右侧颈部无痛性淋巴结病,无任何全身及其他耳鼻喉症状。淋巴结活检报告显示成片的组织细胞浸润,可见吞噬现象,并伴有纤维化和玻璃样变区域。窦组织细胞S-100蛋白呈强阳性。在鉴别诊断巨大或多发淋巴结病时必须考虑罗萨伊-多夫曼病。