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胃肠道原发性淋巴瘤。I. 浆细胞瘤。

Primary lymphomas of the gastrointestinal tract. I. Plasma cell tumours.

作者信息

Henry K, Farrer-Brown G

出版信息

Histopathology. 1977 Jan;1(1):53-76. doi: 10.1111/j.1365-2559.1977.tb01644.x.

DOI:10.1111/j.1365-2559.1977.tb01644.x
PMID:615834
Abstract

The histology of 125 cases of primary gastrointestinal lymphomas arising in the stomach and small and large intestine has been reviewed. The material was gathered from the Bland-Sutton Institute of Pathology at the Middlesex Hospital and from the Westminster Hospital. Of the initial total of 143 cases diagnosed, 18 were rejected. Of the acceptable 125 cases, 51 lymphomas were arising in stomach, 53 in the small intestine and 21 in the large intestine including rectum. Excluding the four children in the series, ages ranged from 18 to 82 and were fairly evenly distributed across the decades. There was no significant sex difference in the Middlesex Hospital cases but in the Westminster Hospital series the male to female ratio was approximately 2.6 to 1. One significant finding to emerge from this histological survey, and which forms the basis of this communication, is the proportion of lymphomas considered to be predominantly of plasma cell type. These plasma cell tumours, or extramedullary plasmacytomas, accounted for 49 out of the 125 cases (39%) of gastrointestinal lymphomas. They were less common in stomach and most common in the intestine, the majority occurring in the ileocaecal region. Conversely, Hodgkin's disease, in contrast to some series, was not encountered. Of the non-Hodgkin's lymphomas, grade I tumours were uncommon and true histiocytic lymphomas were distinctly rare. The high incidence of plasma cell tumours were uncommon and true histiocytic lymphomas were distinctly rare. The high incidence of plasma cell tumours in our series is in keeping with the morphological findings of a previous study carried out in patients with alpha-chain disease and in a small series of primary gastrointestinal lymphomas.

摘要

对125例发生于胃、小肠和大肠的原发性胃肠道淋巴瘤的组织学情况进行了回顾。材料取自米德尔塞克斯医院的布兰德 - 萨顿病理研究所和威斯敏斯特医院。在最初诊断的143例病例中,18例被排除。在可接受的125例病例中,51例淋巴瘤发生于胃,53例发生于小肠,21例发生于包括直肠在内的大肠。该系列中排除4名儿童后,年龄范围为18至82岁,且在各个十年中分布较为均匀。米德尔塞克斯医院的病例中没有明显的性别差异,但在威斯敏斯特医院的系列中,男女比例约为2.6比1。这项组织学调查得出的一个重要发现,也是本交流的基础,是被认为主要为浆细胞类型的淋巴瘤所占比例。这些浆细胞瘤或髓外浆细胞瘤占125例胃肠道淋巴瘤中的49例(39%)。它们在胃中较少见,在肠道中最常见,大多数发生在回盲部。相反,与一些系列不同,未发现霍奇金病。在非霍奇金淋巴瘤中,I级肿瘤不常见,真正的组织细胞淋巴瘤明显罕见。浆细胞瘤的高发病率与先前对α链病患者和一小系列原发性胃肠道淋巴瘤进行的研究的形态学发现一致。

相似文献

1
Primary lymphomas of the gastrointestinal tract. I. Plasma cell tumours.胃肠道原发性淋巴瘤。I. 浆细胞瘤。
Histopathology. 1977 Jan;1(1):53-76. doi: 10.1111/j.1365-2559.1977.tb01644.x.
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Colitis ulcerosa complicated by malignant lymphoma: case report and analysis of published works.溃疡性结肠炎合并恶性淋巴瘤:病例报告及已发表文献分析
Gut. 1995 Feb;36(2):306-10. doi: 10.1136/gut.36.2.306.
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Primary intestinal lymphomas.原发性肠道淋巴瘤
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Primary gastrointestinal lymphoma.原发性胃肠道淋巴瘤
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Rectal malignant lymphoma in chronic ulcerative colitis.慢性溃疡性结肠炎中的直肠恶性淋巴瘤。
Gut. 1982 Feb;23(2):164-8. doi: 10.1136/gut.23.2.164.
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J Clin Pathol. 1978 Nov;31(11):1009-56. doi: 10.1136/jcp.31.11.1009.
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