中国吉林省(白求恩医科大学)非霍奇金淋巴瘤研究

雅潔 張, 昌宏 斉藤, 佳敬 上坂, 勤 綿貫
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摘要

我们对原发性结外非霍奇金淋巴瘤(NHL),特别是胃肠道,以及原发性肠和肠系膜淋巴结淋巴瘤进行了详细的组织病理学和免疫组织化学研究。材料采自中国吉林省。结果:结外NHL 52例,其中胃12例,肠22例(小肠16例,回盲5例,盲肠1例),Waldeyer环11例,其他7例。组织学上弥漫性(D) 45例,滤泡性(F) 7例,D/F比值为6.4:1。表型上,B/T比为25:1。WF分型中恶性43例(82.7%),其中弥漫性大非裂性24例(46.2%)为最优势类型。34例原发性胃肠道淋巴瘤中有5例(14.7%)被重新分类为mocosa-associated lymphoid tissue (MALT)淋巴瘤。3例为中心细胞样细胞(CCL), 2例为大胚样细胞。在所有病例中,淋巴上皮病变(LEL)和反应性或肿瘤性滤泡结构在组织学上都被注意到,并且在CCL和母细胞样细胞中都发现了LN-1的核旁斑点。34例原发性胃肠道淋巴瘤中2例(5.9%)表现为多发性淋巴瘤性息肉病。一个被认为是MALT淋巴瘤播散的结果,因为LEL明显地表现出来,中等大小的细胞核有明显的分裂。另一种确定为多中心起源的套带淋巴瘤,因为模糊结节内的主要成分细胞是小而圆的核,有轻微的分裂,LN-1阴性,LN-2阳性,未发现LEL。原发性小肠和原发性肠系膜淋巴结淋巴瘤之间没有明显的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
中国吉林省(白求恩医科大学)における非ホジキンリンパ腫の研究
A detailed histopathologic and immunohistochemical study has been carried out on primary extranodal non-Hodgkin's lymphoma (NHL), especially in gastrointestinal (GI) tract, and on primary intestinal and mesenteric lymph nodal lymphoma, comparatively. The material were collected from Jilin Provience, China. The results obtained were as follows:A total of 52 cases with extranodal NHL were consisted of 12 of stomach, 22 of intestine (16 of small intestine, 5 of ileocecum and 1 of cecum), 11 of Waldeyer's ring, and 7 of the others.Histologically, 45 cases were diffuse (D) type and the other 7 were follicular (F). D/F ratio was 6.4:1. Phenotypically, B/T ratio was 25:1.According to WF classification, the intermediate grade of malignancy was 43 cases (82.7%) including 24 cases (46.2%) of diffuse, large non-cleaved which was the most preponderant type.Five of 34 cases (14.7%) of primary GI lymphoma were reclassified as mocosa-associated lymphoid tissue (MALT) lymphoma. Three cases were composed of centrocyte-like (CCL) cells and the other 2 were of large blast-like cells. In all cases, the lymphoepithelial lesion (LEL) and reactive or neoplastic follicular structure were noted histologically, and positive finding of paranuclear dot for LN-1, both in CCL and blast-like cells, was found immunohistochemically.Two of 34 cases (5.9%) of primary GI lymphoma showed an appearance of multiple lymphomatous polyposis. The one was recognized as the results of dissemination of MALT lymphoma, because the LEL was distinctively exhibited and the medium-sized cell with nucleus showing marked cleavation. The other was identified as mantle zone lymphoma of multicentric origin, since the main component cells within the vague nodules were small and round nucleus with slight cleavation, negative for LN-1 and positive for LN-2, and no LEL was found.No evident association between the primary small intestinal and the primary mesenteric lymph nodal lymphoma had been recorded.
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