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获得性免疫缺陷综合征中的原发性肾淋巴瘤

Primary lymphoma of the kidney in the acquired immunodeficiency syndrome.

作者信息

Tsang K, Kneafsey P, Gill M J

机构信息

Department of Pathology, Foothills Hospital, Calgary, Alberta, Canada.

出版信息

Arch Pathol Lab Med. 1993 May;117(5):541-3.

PMID:8489348
Abstract

An increased incidence of lymphoma has been reported in patients with the acquired immunodeficiency syndrome. Malignant lymphomas that develop within this setting of impaired immune surveillance have distinctive clinical, histologic, and molecular biologic characteristics. Histologically, the majority of these lymphomas are small noncleaved cell or immunoblastic lymphomas, and are B-cell phenotype by immunophenotypic and immunoglobulin gene rearrangement studies. In contrast with malignant lymphoma occurring in the general population, extranodal origin is common in acquired immunodeficiency syndrome-related non-Hodgkin's lymphomas, with the central nervous system, bone marrow, gastrointestinal tract, and liver being the most common sites. To the best of our knowledge, there has been no description in the literature of primary renal lymphoma occurring in patients with the acquired immunodeficiency syndrome. We report an unusual case of primary non-Hodgkin's lymphoma (diffuse B-cell immunoblastic type) of the kidney in a patient with the acquired immunodeficiency syndrome.

摘要

据报道,获得性免疫缺陷综合征患者淋巴瘤的发病率有所增加。在这种免疫监视受损的情况下发生的恶性淋巴瘤具有独特的临床、组织学和分子生物学特征。组织学上,这些淋巴瘤大多数为小无裂细胞或免疫母细胞淋巴瘤,通过免疫表型和免疫球蛋白基因重排研究显示为B细胞表型。与普通人群中发生的恶性淋巴瘤不同,结外起源在获得性免疫缺陷综合征相关的非霍奇金淋巴瘤中很常见,中枢神经系统、骨髓、胃肠道和肝脏是最常见的部位。据我们所知,文献中尚无关于获得性免疫缺陷综合征患者发生原发性肾淋巴瘤的描述。我们报告了一例获得性免疫缺陷综合征患者发生的不寻常的原发性肾非霍奇金淋巴瘤(弥漫性B细胞免疫母细胞型)。

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