Zhou Zhi-yi, Sun Rong-chao, Yang Shu-dong, Liang Jia-Bei, Rui Jun, Pan Min-hong
Department of Pathology, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, Jiangsu, the People's Republic of China.
Int J Surg Pathol. 2011 Feb;19(1):88-92. doi: 10.1177/1066896909332118. Epub 2009 Feb 17.
Interdigitating dendritic cell tumor/sarcoma is an extremely rare neoplasm that mainly occurs in the lymph node, with only 51 cases reported in the literature to date. The authors report the case of a 41-year-old woman who presented with a 4-month history of a gradually enlarging painless mobile lymphadenopathy in the right submaxillary region. The lymph node mass was completely resected and was treated with 1 cycle of CHOP chemotherapy. After 10 months, she was alive with no evidence of disease. Because interdigitating dendritic cell sarcomas are rare and can show morphologic and immunohistochemical heterogeneity, correct diagnosis requires a high index of suspicion and complete pathological study.
交错突树突状细胞肿瘤/肉瘤是一种极其罕见的肿瘤,主要发生于淋巴结,迄今为止文献中仅报道过51例。作者报告了一名41岁女性的病例,该患者右侧颌下区出现逐渐增大的无痛性可移动淋巴结病,病程4个月。淋巴结肿块被完整切除,并接受了1个周期的CHOP化疗。10个月后,她存活且无疾病证据。由于交错突树突状细胞肉瘤罕见,且可表现出形态学和免疫组化异质性,正确诊断需要高度的怀疑指数和完整的病理研究。