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使用聚合酶链反应(PCR)分析细胞学材料中的克隆性。

Analysis of clonality in cytologic material using the polymerase chain reaction (PCR).

作者信息

Jeffers M D, McCorriston J, Farquharson M A, Stewart C J, Mutch A F

机构信息

Department of Cytology, Glasgow Royal Infirmary, UK.

出版信息

Cytopathology. 1997 Apr;8(2):114-21. doi: 10.1111/j.1365-2303.1997.tb00593.x.

Abstract

Immunoglobulin heavy chain (IgH) gene rearrangement analysis was performed on 27 fine needle aspiration (FNA) specimens (13 reactive hyperplasia, 11 B cell non-Hodgkin's lymphoma (B-NHL), one Hodgkin's disease and two suspicious of non-Hodgkin's lymphoma). Satisfactory amplification was achieved in 23/27 cases. A polyclonal pattern was seen in 14 cases (11 reactive hyperplasia, one B-NHL, one suspicious of lymphoma, one Hodgkin's disease). A monoclonal band was seen in nine cases (eight B-NHL, one reactive hyperplasia). Amplification was unsuccessful in four cases. Clonal analysis by PCR-based IgH gene rearrangement analysis can be successfully applied to FNA material and can be useful in diagnosis, but the results must be interpreted in conjunction with morphology and other ancillary information.

摘要

对27份细针穿刺(FNA)标本进行了免疫球蛋白重链(IgH)基因重排分析(13例反应性增生、11例B细胞非霍奇金淋巴瘤(B-NHL)、1例霍奇金病和2例疑似非霍奇金淋巴瘤)。27例中有23例获得了满意的扩增。14例呈现多克隆模式(11例反应性增生、1例B-NHL、1例疑似淋巴瘤、1例霍奇金病)。9例出现单克隆条带(8例B-NHL、1例反应性增生)。4例扩增失败。基于PCR的IgH基因重排分析进行的克隆分析可成功应用于FNA材料,对诊断有帮助,但结果必须结合形态学及其他辅助信息进行解释。

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