Bao Lei, Wang Ting, Liu Mengyao, Xing Fengjuan
Department of Pathology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University Yantai, People's Republic of China.
Int J Clin Exp Pathol. 2021 Apr 15;14(4):493-500. eCollection 2021.
To explore the clinicopathologic features, immunophenotype, differential diagnosis, and prognosis of tonsil follicular dendritic cell sarcoma (FDCS).
In the Department of Pathology, the affiliated Yantai Yuhuangding Hospital of Qingdao University, in 2019, a case of tonsil FDCS was diagnosed and retrospectively analyzed to summarize its clinical and pathologic characteristics. Relevant literature was reviewed.
The patient was a 71-year-old man. The tumor occurred in the right tonsil with a maximum diameter of 3.5 cm. Microscopically, the tumor cells were spindle-shaped or oval-shaped, arranged in bundles or swirls, and some areas formed concentric circles around blood vessels. Small lymphocytes were distributed in the background. The nucleus was oval-shaped or round, with nuclear chromatin and small central nucleoli. Mitoses were up to 5/10 HPF at the highest. Immunohistochemistry showed positive expression of CD21, CD23, CD68, vimentin, and D2-40 in tumor cells, and Ki67 proliferation index was about 20%. CXCL13 was positive only in scattered background lymphocytes. In situ hybridization for EBER was negative. After surgical resection of the tumor, without radiotherapy or chemotherapy, the patient has been followed up for 4 months until now, without recurrence or metastasis.
FDCS is a rare tumor, especially in extranodal sites. The pathogenesis, treatment and prognosis of FDCS still need further exploration.
探讨扁桃体滤泡树突状细胞肉瘤(FDCS)的临床病理特征、免疫表型、鉴别诊断及预后。
青岛大学附属烟台毓璜顶医院病理科于2019年诊断1例扁桃体FDCS,并进行回顾性分析,总结其临床及病理特征。同时复习相关文献。
患者为71岁男性。肿瘤发生于右侧扁桃体,最大直径3.5 cm。镜下,肿瘤细胞呈梭形或椭圆形,呈束状或漩涡状排列,部分区域围绕血管形成同心圆。背景中有小淋巴细胞分布。细胞核呈椭圆形或圆形,有核染色质及小的中央核仁。最高有丝分裂象达5/10 HPF。免疫组化显示肿瘤细胞CD21、CD23、CD68、波形蛋白及D2-40呈阳性表达,Ki67增殖指数约为20%。CXCL13仅在散在的背景淋巴细胞中呈阳性。EBER原位杂交为阴性。肿瘤手术切除后,未行放疗或化疗,目前患者已随访4个月,无复发及转移。
FDCS是一种罕见肿瘤,尤其发生于结外部位。FDCS的发病机制、治疗及预后仍需进一步探索。