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[聚合酶链反应在细针穿刺细胞学标本诊断B型非霍奇金淋巴瘤中的应用]

[Application of PCR in the diagnosis of B-type non-Hodgkin's lymphomas in cytological specimens from fine-needle aspiration].

作者信息

Movilia A, De Servi B, Assi A

机构信息

Unità Operativa di Anatomia e Istologia Patologica, Azienda Ospedaliera, Ospedale Civile di Legnano.

出版信息

Pathologica. 2000 Jun;92(3):172-6.

Abstract

UNLABELLED

The application of PCR to detect monoclonality at the immunoglobulin heavy chain gene locus in FNA cytologic specimens was evaluated.

MATERIALS AND METHODS

Immunoglobulin heavy chain gene rearrangement analysis was performed by a nested PCR for the VDJ region on 27 lymph nodes FNA paraffin embedded by cell blocking technique specimens (1 suspicious of NOS lymphoma, 1 Hodgkin's disease, 6 B cell non Hodgkin's lymphomas, 10 reactive hyperplasias).

RESULTS

A monoclonal band was seen in 13 of 17 suspicious or positive malignant cases. The other 4 specimens gave a policlonal pattern. Specimens from reactive lymph nodes produced policlonal bands in 8 cases, no product in 1 case and 1 specimen gave a monoclonal band. When needed, the results of PCR examinations were compared with the subsequent histologic evaluation of the same lymph-node.

CONCLUSIONS

From our experience we can see that clonal analysis by PCR based IgH gene rearrangement analysis can be applied to FNA material and can be useful in diagnosis.

摘要

未标记

评估了聚合酶链反应(PCR)在细针穿刺(FNA)细胞学标本的免疫球蛋白重链基因位点检测单克隆性中的应用。

材料与方法

采用巢式PCR对27例经细胞块技术包埋的FNA石蜡包埋淋巴结标本(1例疑似未另行分类淋巴瘤、1例霍奇金病、6例B细胞非霍奇金淋巴瘤、10例反应性增生)的VDJ区域进行免疫球蛋白重链基因重排分析。

结果

17例可疑或阳性恶性病例中有13例出现单克隆条带。其他4份标本呈现多克隆模式。反应性淋巴结标本8例产生多克隆条带,1例无产物,1份标本出现单克隆条带。必要时,将PCR检测结果与同一淋巴结随后的组织学评估结果进行比较。

结论

根据我们的经验,基于PCR的免疫球蛋白重链基因重排分析进行的克隆分析可应用于FNA材料,对诊断有帮助。

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