首页> 外文期刊>National Journal of Community Medicine >Mantle Cell Lymphoma of GI Tract Presented as Multiple Lymphomatous Polyposis: A Rare Intestinal Malignancy
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Mantle Cell Lymphoma of GI Tract Presented as Multiple Lymphomatous Polyposis: A Rare Intestinal Malignancy

机译:表现为多发性淋巴息肉病的胃肠道套细胞淋巴瘤:罕见的肠恶性肿瘤。

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Primary lymphomas arising in the large intestine are less frequent than either gastric or small bowel lymphomas. Primary colorectal lymphomas account for about 0.2% of all neoplasm. Mantle cell lymphoma in form of multiple lymphomatous polyposis is less frequent in colorectum than in the small bowel.2 We present a case of 68 year-old man suffered from abdominal pain and diarrhoea for one year with complain of blood in stool for last 15 days. Multiple polypoid masses were found in the entire colon and caecum on colonoscopic examination. Computerized tomography of the abdomen revealed a large soft tissue mass lesion in caecum and ascending colon with diffuse polypoidal wall thickening involving the transverse colon, sigmoid colon, descending colon with mesenteric lymph node enlargement. Colonoscopic excision of polyp from ascending colon and transverse colon was done. The histological diagnosis was Non-Hodgkin lymphoma with multiple lymphomatous polyposis. In immunohitochemistry, there was positive staining for CD20, CD 5 and cyclin D1 and suggestive of mantle cell lymphoma B cell type. MCL is an aggressive lymphoma, which typically presents in advanced stage; there is often involvement of mesenteric and peripheral lymph nodes, spleen, bone marrow and peripheral blood 6.
机译:在大肠中发生的原发性淋巴瘤的发生率低于胃或小肠淋巴瘤。原发性大肠淋巴瘤约占所有肿瘤的0.2%。多发性淋巴瘤性息肉病形式的套细胞淋巴瘤在大肠癌中的发生频率比在小肠中低。2我们提供了一个案例,该例为一名68岁的男性,患腹部疼痛和腹泻一年,最近15天便血。结肠镜检查发现整个结肠和盲肠有多个息肉样肿块。腹部计算机断层扫描显示,盲肠和升结肠有较大的软组织肿块,弥漫性息肉样壁增厚,累及横结肠,乙状结肠,降结肠,肠系膜淋巴结肿大。结肠镜检查息肉从升结肠和横结肠切除。组织学诊断为非霍奇金淋巴瘤伴多发性淋巴瘤性息肉。在免疫组织化学中,CD20,CD 5和细胞周期蛋白D1呈阳性染色,提示其为B型淋巴瘤细胞。 MCL是一种侵袭性淋巴瘤,通常表现为晚期。肠系膜和外周淋巴结,脾脏,骨髓和外周血常受累6。

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