Follicular dendritic cell sarcoma of the nasopharynx: a case report and literature review

Na Xiao, Shubing Xiao, Wei-Jia Yang
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引用次数: 1

Abstract

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1例报告并文献复习
鼻咽部滤泡状树突状细胞肉瘤(FDCS)是一种罕见的恶性肿瘤,仅在少数病例报告中被描述,其鉴别诊断包括多种临床病理实体。FDCS最初常常被误诊,特别是在检查小活检标本时。我们在此报告一例发生于鼻咽部的FDCS,最初被误诊为神经鞘肿瘤。一位44岁的女性表现为持续阻塞的左鼻腔,并接受了切除活检。标本表现出FDCS的形态学和免疫组织化学特征。Epstein-Barr病毒编码RNA的原位杂交为阴性。病人接受了化疗和放疗。最初治疗3年后,肉瘤在原发部位附近复发,并被完全切除。在撰写本文时,患者在切除后无病1年。报告本病例是为了提高临床对FDCS的认识。
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