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胃肠道套叠表现的套细胞淋巴瘤——病例报告及文献复习

Mantle cell lymphoma of the gastrointestinal tract presenting with multiple intussusceptions--case report and review of literature.

作者信息

Kella Venkata K N, Constantine Radu, Parikh Nalini S, Reed Mary, Cosgrove John M, Abo Stephen M, King Saundra

机构信息

Department of Surgery and Oncology, Bronx-Lebanon Hospital Center, Bronx, New York, USA.

出版信息

World J Surg Oncol. 2009 Jul 31;7:60. doi: 10.1186/1477-7819-7-60.

Abstract

BACKGROUND

Mantle cell lymphoma (MCL) is an aggressive type of B-cell non-Hodgkin's lymphoma that originates from small to medium sized lymphocytes located in the mantle zone of the lymph node. Extra nodal involvement is present in the majority of cases, with a peculiar tendency to invade the gastro-intestinal tract in the form of multiple lymphomatous polyposis. MCL can be accurately diagnosed with the use of the highly specific marker Cyclin D1. Few cases of mantle cell lymphoma presenting with intussuception have been reported. Here we present a rare case of multiple intussusceptions caused by mantle cell lymphoma and review the literature of this disease.

CASE PRESENTATION

A 68-year-old male presented with pain, tenderness in the right lower abdomen, associated with nausea and non-bilious vomiting. CT scan of abdomen revealed ileo-colic intussusception. Laparoscopy confirmed multiple intussusceptions involving ileo-colic and ileo-ileal segments of gastrointestinal tract. A laparoscopically assisted right hemicolectomy and extended ileal resection was performed. Postoperative recovery was uneventful. The histology and immuno-histochemistry of the excised small and large bowel revealed mantle cell lymphoma with multiple lymphomatous polyposis and positivity to Cyclin D1 marker. The patient was successfully treated with Rituximab-CHOP chemotherapy and remains in complete remission at one-year follow-up.

CONCLUSION

This is a rare case of intestinal lymphomatous polyposis due to mantle cell lymphoma presenting with multiple small bowel intussusceptions. Our case highlights laparoscopic-assisted bowel resection as a potential and feasible option in the multi-disciplinary treatment of mantle cell lymphoma.

摘要

背景

套细胞淋巴瘤(MCL)是一种侵袭性B细胞非霍奇金淋巴瘤,起源于位于淋巴结套区的中小淋巴细胞。大多数病例存在结外受累,特别倾向于以多发性淋巴瘤性息肉病的形式侵犯胃肠道。使用高度特异性标志物细胞周期蛋白D1可准确诊断MCL。报道的套细胞淋巴瘤表现为肠套叠的病例很少。在此,我们报告一例由套细胞淋巴瘤引起的罕见多发性肠套叠病例,并复习该疾病的文献。

病例报告

一名68岁男性,出现右下腹疼痛、压痛,伴有恶心和非胆汁性呕吐。腹部CT扫描显示回结肠套叠。腹腔镜检查证实胃肠道的回结肠和回肠段存在多发性套叠。进行了腹腔镜辅助右半结肠切除术和扩大的回肠切除术。术后恢复顺利。切除的小肠和大肠的组织学及免疫组织化学检查显示为套细胞淋巴瘤,伴有多发性淋巴瘤性息肉病,且细胞周期蛋白D1标志物呈阳性。患者接受利妥昔单抗-CHOP化疗成功治疗,随访一年仍处于完全缓解状态。

结论

这是一例罕见的因套细胞淋巴瘤导致肠道淋巴瘤性息肉病并表现为多发性小肠套叠的病例。我们的病例强调了腹腔镜辅助肠切除术作为套细胞淋巴瘤多学科治疗中一种潜在且可行的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fd4/2732623/0fe92c56bc83/1477-7819-7-60-1.jpg

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