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X 线淋巴肉芽肿病(LgrX)/血管免疫母细胞性淋巴结病(AILD)中的染色体异常

Chromosomal abnormalities in lymphogranulomatosis X (LgrX)/angioimmunoblastic lymphadenopathy (AILD).

作者信息

Gödde-Salz E, Feller A C, Lennert K

出版信息

Leuk Res. 1987;11(2):181-90. doi: 10.1016/0145-2126(87)90024-5.

Abstract

Histologically, lymphogranulomatosis X (LgrX) is a Morbus Hodgkin-like disease which until now has been considered as an abnormal immune reaction or a prelymphoma. Chromosome analyses showed that LgrX and angioimmunoblastic lymphadenopathy AILD) are characterized by chromosomal aberrations. Chromosome analyses of 18 cases of LgrX with sequential banding techniques showed abnormalities in 13 out of 18 cases. They were monoclonal in 7 cases. The most frequent abnormalities were trisomies of chromosomes Nos 3 and 5 and duplication of the X-chromosome. The abnormal karyotypes always appeared with normal mitosis in single or clonal cells. They were found in unstimulated and in PHA-stimulated cultures from lymph node and peripheral blood. Thus, it can be concluded that at least some cases of LgrX are monoclonal cell proliferations. An attempt is made to define the role of chromosomal abnormalities in the development of malignant lymphomas.

摘要

从组织学上看,X 线淋巴肉芽肿病(LgrX)是一种类霍奇金病,迄今为止一直被视为一种异常免疫反应或淋巴瘤前期病变。染色体分析表明,LgrX 和血管免疫母细胞性淋巴结病(AILD)的特征是染色体畸变。采用连续显带技术对 18 例 LgrX 进行染色体分析,结果显示 18 例中有 13 例存在异常。其中 7 例为单克隆性。最常见的异常是 3 号和 5 号染色体三体以及 X 染色体重复。异常核型总是出现在单个或克隆细胞的正常有丝分裂中。在未刺激的以及来自淋巴结和外周血的PHA 刺激培养物中均发现了这些异常。因此,可以得出结论,至少部分 LgrX 病例是单克隆细胞增殖。本文试图明确染色体异常在恶性淋巴瘤发生发展中的作用。

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