Mantle cell lymphoma of the colon: case report and literature review.

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2025-05-30 eCollection Date: 2025-05-01 DOI:10.1093/jscr/rjaf347
Gregory Crisafulli, Pasha Shenasan, Aakash Trivedi, Nawras Radwan, Abraham El-Sedfy
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引用次数: 0

Abstract

Primary extranodal lymphoma is a rare presentation of B-cell non-Hodgkin's lymphoma (NHL), most commonly found in the gastrointestinal tract. Mantle cell lymphoma (MCL), a rare and aggressive subtype, accounts for only 2.5% of all lymphoid neoplasms and is less commonly localized in the colon. We present a 79-year-old man with abdominal pain and nausea. Imaging revealed cecal wall thickening with ileocolic intussusception. Colonoscopy identified a circumferential cecal mass, necessitating robotic-assisted right hemicolectomy. Final pathology confirmed MCL. The patient recovered well without complications. Colorectal MCL is a rare and aggressive NHL variant requiring a multidisciplinary approach. Surgery plays a crucial role in managing complications and localized disease. Given the lack of standardized treatment protocols, further research is needed to optimize therapeutic strategies and long-term outcomes.

结肠套细胞淋巴瘤:1例报告及文献复习。
原发性结外淋巴瘤是一种罕见的b细胞非霍奇金淋巴瘤(NHL),最常见于胃肠道。套细胞淋巴瘤(MCL)是一种罕见的侵袭性亚型,仅占所有淋巴样肿瘤的2.5%,不常局限于结肠。我们报告一位79岁的男性腹痛和恶心。影像显示盲肠壁增厚伴回结肠肠套叠。结肠镜检查发现环状盲肠肿块,需要机器人辅助右半结肠切除术。最终病理证实为MCL。病人恢复良好,无并发症。结直肠MCL是一种罕见的侵袭性NHL变体,需要多学科联合治疗。手术在治疗并发症和局部疾病中起着至关重要的作用。由于缺乏标准化的治疗方案,需要进一步的研究来优化治疗策略和长期结果。
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
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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