A Single Colonic Polyp Having Both Tubular Adenoma and Mantle Cell Lymphoma: A Case Report.

IF 0.7 Q4 GASTROENTEROLOGY & HEPATOLOGY
Case Reports in Gastroenterology Pub Date : 2025-10-21 eCollection Date: 2025-01-01 DOI:10.1159/000548048
Dua Abuquteish, Ahmed Al-Azzeh, Sami Bannoura
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Abstract

Introduction: Mantle cell lymphoma (MCL) is a distinct subtype of B-cell non-Hodgkin lymphoma. MCL lymphoma can occur in the gastrointestinal tract (GIT) as a primary lymphoma; more commonly, the GIT can be secondarily involved. A colonic polyp simultaneously having MCL with overlying adenomatous changes is highly unusual, and few cases were reported. Herein, we describe a unique instance of a single adenomatous polyp in the left colon overlying a small lymphoid population proven to be MCL in a patient recently diagnosed with MCL. We believe this report will increase the awareness of pathologists and clinicians of such a unique and unusual clinical presentation.

Case presentation: A 53-year-old male patient presented with a history of generalized lymphadenopathy, bilateral pleural deposits, and splenomegaly. Axillary lymph node excisional biopsies were sent for pathology and reported MCL, diffuse pattern, classic variant. Three weeks later, the patient underwent upper and lower endoscopy for mild upper abdominal discomfort. Upper endoscopy showed mild gastropathy, and colonoscopy revealed a small polyp at the descending colon. Pathology of the colonic polyp showed a tubular adenoma with low-grade dysplasia overlying a well-circumscribed mucosal/submucosal nodular lymphoid aggregate. The lymphoid aggregate exhibited histological and immunohistochemical features of MCL. Thus, a diagnosis of tubular adenoma coexisting with MCL in the same polyp was made.

Conclusion: Tubular adenoma with MCL is an exceedingly rare phenomenon with unclear pathogenesis. We report this case to highlight the importance of examining lymphoid tissue in adenomas and to increase the awareness among clinicians and pathologists of such a unique presentation.

Abstract Image

Abstract Image

单结肠息肉合并管状腺瘤和套细胞淋巴瘤1例。
套细胞淋巴瘤(MCL)是一种独特的b细胞非霍奇金淋巴瘤亚型。MCL淋巴瘤可发生在胃肠道(GIT)作为原发性淋巴瘤;更常见的是,GIT可能是次要的。结肠息肉同时有MCL并上覆腺瘤改变是非常罕见的,报告的病例很少。在这里,我们描述了一个独特的例子,一个单一的腺瘤性息肉在左结肠上的小淋巴细胞群被证明是MCL的患者最近被诊断为MCL。我们相信这份报告将增加病理学家和临床医生的认识,这样一个独特的和不寻常的临床表现。病例介绍:一名53岁男性患者,有广泛性淋巴结病、双侧胸膜沉积和脾肿大病史。腋窝淋巴结切除活检病理报告MCL,弥漫性模式,经典变种。三周后,患者因轻度上腹部不适行上下内窥镜检查。上镜检查显示轻度胃病,结肠镜检查显示降结肠有小息肉。结肠息肉的病理显示一个低级别发育不良的管状腺瘤覆盖在边界清晰的粘膜/粘膜下结节性淋巴样聚集体上。淋巴样聚集体表现出MCL的组织学和免疫组织化学特征。因此,在同一息肉中诊断为管状腺瘤与MCL共存。结论:管状腺瘤合并MCL是一种极为罕见的现象,其发病机制尚不清楚。我们报告这个病例是为了强调在腺瘤中检查淋巴组织的重要性,并提高临床医生和病理学家对这种独特表现的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Gastroenterology
Case Reports in Gastroenterology Medicine-Gastroenterology
CiteScore
1.10
自引率
0.00%
发文量
99
审稿时长
7 weeks
期刊介绍:
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