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南非的原发性肠道淋巴瘤。

Primary intestinal lymphoma in South Africa.

作者信息

Novis B H

出版信息

Isr J Med Sci. 1979 Apr;15(4):386-9.

PMID:109420
Abstract

All adult cases of primary intestinal lymphoma seen during the years 1953--77 at Groote Schuur Hospital, South Africa, were reviewed. Seventy percent of patients with solitary lymphoma and 80% with immunoproliferative small intestinal disease were mulatto. Patients in the latter group presented with malabsorption and those with a solitary lymphoma presented with intestinal obstruction. Four of 15 patients tested for the presence of alpha-heavy-chains were found to have alpha-heavy-chain disease. Family studies of potential genetic and immunologic factors showed some significant differences in IgA and IgG levels in the families of two patients with alpha-heavy-chain disease. Elevated alkaline phosphatase of intestinal origin was found in four of six patients with immunoproliferative small intestinal disease and in a high proportion of relatives. Fifty percent of the six patients were of blood group B. Minor blood groups, ABH secretor state and Pi phenotype distribution were similar to those of the control subjects. HLA gene frequency was particularly increased in the HLA-A9 antigen. These studies suggest that genetic factors may be relevant to the pathogenesis of immunoproliferative small intestinal disease.

摘要

对1953年至1977年期间在南非格罗特·舒尔医院就诊的所有原发性肠道淋巴瘤成年病例进行了回顾。孤立性淋巴瘤患者中有70%以及免疫增殖性小肠疾病患者中有80%是混血儿。后一组患者表现为吸收不良,而孤立性淋巴瘤患者表现为肠梗阻。在15名检测α重链的患者中,有4人被发现患有α重链病。对潜在遗传和免疫因素的家族研究表明,两名α重链病患者的家族中,IgA和IgG水平存在一些显著差异。在6名免疫增殖性小肠疾病患者中有4人以及相当比例的亲属中发现肠道来源的碱性磷酸酶升高。这6名患者中有50%是B血型。次要血型、ABH分泌状态和Pi表型分布与对照组相似。HLA基因频率在HLA - A9抗原中尤其升高。这些研究表明,遗传因素可能与免疫增殖性小肠疾病的发病机制有关。

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