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EB 病毒阳性炎症性滤泡树突状细胞肉瘤表现为孤立性结肠肿块:两例罕见病例并文献复习。

Epstein-Barr virus-positive inflammatory follicular dendritic cell sarcoma presenting as a solitary colonic mass: two rare cases and a literature review.

机构信息

Department of Pathology, Renmin Hospital of Wuhan University, Wuhan, China.

Department of Pathophysiology, School of Basic Medicine, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Histopathology. 2020 Nov;77(5):832-840. doi: 10.1111/his.14169. Epub 2020 Sep 23.

DOI:10.1111/his.14169
PMID:32506505
Abstract

AIMS

Follicular dendritic cell (FDC) sarcoma is a rare neoplasm originating from follicular dendritic cells in germinal centres. It is classified as conventional and Epstein-Barr virus (EBV)-positive inflammatory FDC sarcoma according to the 2019 World Health Organization classification of digestive system tumours; the latter is rarer. So in view of the rarity and difficulty in diagnosis, the aim of the manuscript is to share our experience of diagnosing EBV-positive inflammatory FDC sarcoma.

METHODS AND RESULTS

Here, we describe the clinicopathological features, gross description, histomorphology, immunophenotype, EBV-encoded mRNA (EBER) in-situ hybridisation, gene rearrangement and clinical follow-up of two patients with EBV-positive inflammatory FDC sarcoma in the colon, and review the relevant literature. The tumours were found in two males, aged 53 and 48 years, respectively, with a tumour diameter between 10 and 45 mm. Both cases occurred in the colon and presented as pedunculated colonic masses. Microscopically, scanty atypical ovoid to spindle neoplastic cells were mixed in a background of florid lymphoplasmacytic infiltration. The nuclei of these atypical cells showed vesicular chromatin and small, distinct nucleoli. Immunohistochemistry demonstrated that the atypical stromal cells were positive for CD21, CD23, CD35, and D2-40. EBER in-situ hybridisation also gave positive results in two cases. There was a mean follow-up of 9 months (range, 7-11 months).

CONCLUSION

EBV-positive inflammatory FDC sarcoma is an extremely rare tumour with a distinct morphology and phenotype. Therefore, it is very important to recognise it particularly for correct diagnosis and prevention of misdiagnosis and mistreatment.

摘要

目的

滤泡树突细胞(FDC)肉瘤是一种罕见的肿瘤,起源于生发中心的滤泡树突细胞。根据 2019 年世界卫生组织消化系统肿瘤分类,它可分为常规型和 EBV 阳性炎症性 FDC 肉瘤;后者较为罕见。鉴于其罕见性和诊断难度,本文旨在分享我们对 EBV 阳性炎症性 FDC 肉瘤的诊断经验。

方法和结果

在此,我们描述了两位 EBV 阳性炎症性 FDC 肉瘤患者的临床病理特征、大体描述、组织形态学、免疫表型、EBV 编码的 mRNA(EBER)原位杂交、基因重排和临床随访,并复习了相关文献。这两个肿瘤均发生在 53 岁和 48 岁的男性,肿瘤直径分别为 10-45mm。两个病例均发生在结肠,表现为带蒂的结肠肿块。显微镜下,稀疏的非典型卵圆形至梭形肿瘤细胞与丰富的淋巴浆细胞浸润混合存在。这些非典型细胞的核呈泡状染色质,有小而明显的核仁。免疫组织化学显示,这些非典型基质细胞 CD21、CD23、CD35 和 D2-40 阳性。EBER 原位杂交在两个病例中也呈阳性。平均随访时间为 9 个月(7-11 个月)。

结论

EBV 阳性炎症性 FDC 肉瘤是一种形态和表型独特的极罕见肿瘤。因此,认识到这一点非常重要,尤其是为了正确诊断,防止误诊和误治。

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