Master Degree Candidate, Department of Pathology, Xiantao First People's Hospital of Yangtze University, Xiantao, China.
Undergraduate, Department of Pathology, Xiantao First People's Hospital of Yangtze University, Xiantao, China.
J Int Med Res. 2022 May;50(5):3000605221097662. doi: 10.1177/03000605221097662.
Follicular dendritic cell sarcoma (FDCS) of the nasopharynx is a rare malignant tumor that has been described in only a few case reports, and its differential diagnoses include diverse clinicopathologic entities. FDCS is often initially misdiagnosed, especially when examining small biopsy specimens. We herein report a case of FDCS arising in the nasopharynx that was initially misdiagnosed as a nerve sheath tumor. A 44-year-old woman presented with persistent obstruction of the left nasal cavity and underwent an excisional biopsy. The specimen demonstrated morphologic and immunohistochemical features of FDCS. In situ hybridization for Epstein-Barr virus-encoded RNA was negative. The patient was treated with chemotherapy and radiotherapy. The sarcoma recurred near the original site more than 3 years after the initial treatment and was completely resected. At the time of this writing, the patient had remained disease-free for 1 year after resection. This case is being reported to improve the clinical recognition of FDCS.
鼻咽部滤泡树突状细胞肉瘤(FDCS)是一种罕见的恶性肿瘤,仅在少数病例报告中有所描述,其鉴别诊断包括多种临床病理实体。FDCS 常被误诊,尤其是在检查小的活检标本时。本文报告了一例发生在鼻咽部的 FDCS 病例,最初误诊为神经鞘瘤。一名 44 岁女性因左侧鼻腔持续阻塞而就诊,并接受了切除术活检。该标本显示出 FDCS 的形态学和免疫组织化学特征。原位杂交检测 EBV 编码 RNA 为阴性。患者接受了化疗和放疗。肉瘤在初始治疗后 3 年以上在原部位附近复发,并被完全切除。在撰写本文时,患者在切除后 1 年仍无疾病。本病例旨在提高对 FDCS 的临床认识。