Yu Lu, Yang Shou Jing
Pathology, Xi Jing Hospital, 4th Military Medical University, Xi'an, Shaanxi 710032, China.
Int J Surg Pathol. 2011 Aug;19(4):502-5. doi: 10.1177/1066896909335507. Epub 2009 May 15.
Follicular dendritic cell (FDC) sarcoma, especially of extranodal origin, is an extremely rare malignancy of FDC origin, with only 1 case previously documented in the thyroid. The authors report the case of a 58-year-old female who presented with a painless mass in her neck. The neoplastic cells expressed monocyte/macrophage-specific marker CD68 (KP-1) and lysozymes and the dendritic cell-associated antigens CD35 and Fascin but was negative for CD1a, CD21, and CD23, most consistent with a diagnosis of FDC sarcoma. BIOMED-2 multiplex polymerase chain reaction analysis showed B-cell clonality in both tumor and its adjacent coexisting Hashimoto's thyroiditis. To the authors' knowledge, this is the first report of a rare entity of FDC sarcoma primarily involving the thyroid gland coexisting with Hashimoto's thyroiditis.
滤泡树突状细胞(FDC)肉瘤,尤其是结外起源的,是一种极其罕见的起源于FDC的恶性肿瘤,此前仅有1例记录于甲状腺。作者报告了1例58岁女性患者,该患者颈部出现无痛性肿块。肿瘤细胞表达单核细胞/巨噬细胞特异性标志物CD68(KP-1)和溶菌酶以及树突状细胞相关抗原CD35和Fascin,但CD1a、CD21和CD23呈阴性,最符合FDC肉瘤的诊断。BIOMED-2多重聚合酶链反应分析显示肿瘤及其相邻并存的桥本甲状腺炎均存在B细胞克隆性。据作者所知,这是首例罕见的主要累及甲状腺的FDC肉瘤与桥本甲状腺炎并存的报告。