Agarwal Atin, Pathak Suniti, Gujral Sumeet
Department of Pathology, Tata Memorial Hospital, Parel, Mumbai.
Indian J Pathol Microbiol. 2006 Oct;49(4):509-15.
Sinus histiocytosis with massive lymphadenopathy (SHML) also called as Rosai Dorfman disease is a rare histiocytic proliferative disorder of unknown etiology. Histological features currently define it. Persistent painless lymphadenopathy due to expansion of sinuses infiltrated with benign histiocytes and plasma cells and emperipolesis are the characteristic features of SHML. Our study includes seven cases (5 nodal and 2 extranodal) of SHML over a 5-year period whose slides and blocks were reviewed. IHC was performed on the main lesion, from a panel of S100, CD68, LCA, CD20, CD3, CD30, CD43, bcl2, cytokeratin and epithelial membrane antigen. In our series we have work up available in 7 cases out of which a detailed follow-up is available in 5 patients. Out of these 5 patients, 4 have a stable disease, while one developed histiocytic sarcoma after a gap of four years.
伴巨大淋巴结病的窦组织细胞增生症(SHML),也称为罗萨伊-多夫曼病,是一种病因不明的罕见组织细胞增生性疾病。目前通过组织学特征对其进行定义。由于充满良性组织细胞和浆细胞的窦扩张以及血细胞吞噬作用导致的持续性无痛性淋巴结病是SHML的特征性表现。我们的研究纳入了5年期间的7例SHML病例(5例淋巴结型和2例结外型),对其切片和组织块进行了复查。对主要病变进行了免疫组化检测,检测指标包括S100、CD68、LCA、CD20、CD3、CD30、CD43、bcl2、细胞角蛋白和上皮膜抗原。在我们的系列研究中,7例病例均有相关检查结果,其中5例患者有详细的随访资料。在这5例患者中,4例病情稳定,1例在4年后发展为组织细胞肉瘤。