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直肠扁桃体3例临床病理特征并文献复习OACSTPCD

Rectal tonsil:Clinicopathological features of 3 cases and literature review

中文摘要英文摘要

目的:直肠扁桃体(rectal tonsil,RT)是一种直肠内淋巴组织反应性增生的良性病变,但临床罕见,易误诊.本文通过探讨RT的临床病理特征、鉴别和诊断,旨在提高对该疾病的认识.方法:对3例诊断为RT患者的临床病理特征和免疫表型结果进行分析,并复习相关文献.结果:3例RT患者均为男性,年龄为6~71岁,临床症状为便秘、便血或肛门脱出包块,肠镜下见息肉样隆起.RT低倍镜下黏膜层及黏膜下层可见淋巴细胞及浆细胞浸润,形成大小不等、形态多样的淋巴滤泡结构.高倍镜下细胞未见明显异型,部分区可见核分裂象.免疫组织化学表达T细胞标志(CD3、CD5)和B细胞标志(CD20),生发中心阳性表达CD10和B细胞淋巴瘤(B cell lymphoma,Bcl)-6,不表达Bcl-2.CD21勾勒出完整的滤泡树突状细胞(follicular dendritic cell,FDC)网.3例Epstein-Barr病毒编码的小RNA(Epstein-Barr virus encoded RNAs,EBER)检测均为阴性.3例患者均行"息肉"切除,术后随访4~20个月未见复发和转移.结论:RT是一种病因不明,临床罕见,尚未被广泛认识的疾病,掌握其临床病理特征十分重要,确诊依赖于病理学检查.

Objective:Rectal tonsil(RT)is a benign lesion characterized by reactive hyperplasia of lymphoid tissue within the rectum.It is clinically rare and easily misdiagnosed.This article aims to improve the understanding of RT by discussing its clinicopathological features,differentiation,and diagnosis. Methods:Clinicopathologic features and immunophenotype results of 3 patients diagnosed with RT were analyzed retrospectively,and relevant literature was reviewed. Results:All three RT patients were male,aged 6 to 71 years,presenting with clinical symptoms such as constipation,hematochezia,or anal protruding masses.Colonoscopy showed polyp-like elevations.Low-power microscopy showed lymphocyte and plasma cell infiltration in the mucosal and submucosal layers,forming variably sized and shaped lymphoid follicle structures.High-power microscopy did not reveal significant cellular atypia,although mitotic figures were observed in some areas.Immunohistochemically,T-cell markers(CD3,CD5)and B-cell markers(CD20)were expressed,with germinal centers expressing CD10 and B-cell lymphoma(Bcl)-6,but not Bcl-2.CD21 outlined a complete follicular dendritic cell(FDC)network.All three cases tested negative for Epstein-Barr virus encoded RNAs(EREB).The patients underwent polyp resection,with no recurrence or metastasis observed during the follow-up period of 4 to 20 months. Conclusion:RT is a relatively rare and not widely recognized disease of unknown etiology.Understanding its clinicopathological features is crucial,and diagnosis relies on pathological examination.

赵为璘;王新红;袁玲玲;王铁延

十堰市太和医院,湖北医药学院附属医院病理科,湖北十堰 442000

直肠扁桃体临床病理特征免疫组织化学

rectal tonsilclinicopathological featuresimmunohistochemistry

《临床与病理杂志》 2024 (003)

463-467 / 5

10.11817/j.issn.2095-6959.2024.230454

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