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聚合酶链反应在小B细胞非霍奇金淋巴瘤诊断中的应用

The Polymerase Chain Reaction in Diagnosis of Small B-Cell Non-Hodgkin Lymphomas.

作者信息

Antoro Ester Lianawati, Dwianingsih Ery Kus, Triningsih Fx Ediati

机构信息

Department of Anatomical Pathology, Faculty of Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia E-mail :

出版信息

Asian Pac J Cancer Prev. 2016;17(2):491-5. doi: 10.7314/apjcp.2016.17.2.491.

Abstract

BACKGROUND

Small B-cell non-Hodgkins lymphoma (NHL) is difficult to be distinguished from non-neoplastic reactive processes using conventional haematoxylin-eosin (HE) staining due to different interpretations among pathologists with diagnosis based on morphologic features. Ancillary examinations such as immunohistochemical (IHC) staining are essential. However, negative or doubtful results are still sometimes obtained due to unsatisfactory tissue processing or IHC technique. The polymerase chain reaction (PCR) as a molecular diagnostic technique is very sensitive and specific. Clonality detection of heavy chain immunoglobulin (IgH) gene rearrangement has been widely used to establish diagnosis of B-cell NHL.

AIMS

To elaborate interobserver variation in small B-cell NHL diagnosis based on morphologic features only and to confirm sensitivity and specificity of the PCR technique as an ancillary method.

MATERIALS AND METHODS

A toptal of 28 samples of small B cell NHL and suspicious lymphoma were interpreted by 3 pathologists in Sardjito General Hospital based on their morphology only. The reliability of assessment and the coefficient of interobserver agreement were calculated by Fleiss kappa statistics. Interpretation results were confirmed with IHC staining (CD20, CD3, Bcl2). PCR was performed to analyze the clonality of IgH gene rearrangement.

RESULTS

Interobserver agreement in morphologic evalution of small B cell NHL and chronic lymphadenitis revealed kappa coefficient 0.69 included in the substantial agreement category. The cases were divided into 3 groups based on morphology and IHC results; lymphoma, reactive process and undetermined group. PCR analysis showed 90% sensitivity and 60% specificity.

CONCLUSIONS

The present study revealed a substantial agreement among pathologists in small B-cell NHL diagnosis. For difficult cases, PCR is useful as complementary method to morphologic and IHC examinations to establish definitive diagnosis.

摘要

背景

小B细胞非霍奇金淋巴瘤(NHL)由于病理学家基于形态学特征进行诊断时存在不同解读,使用传统苏木精-伊红(HE)染色难以与非肿瘤性反应性病变相区分。免疫组织化学(IHC)染色等辅助检查至关重要。然而,由于组织处理或免疫组化技术不理想,有时仍会获得阴性或可疑结果。聚合酶链反应(PCR)作为一种分子诊断技术非常敏感且特异。重链免疫球蛋白(IgH)基因重排的克隆性检测已广泛用于确诊B细胞NHL。

目的

阐述仅基于形态学特征诊断小B细胞NHL时观察者间的差异,并确认PCR技术作为辅助方法的敏感性和特异性。

材料与方法

印度尼西亚日惹萨迪托综合医院的3位病理学家仅根据形态学对28例小B细胞NHL和可疑淋巴瘤样本进行解读。通过Fleiss卡方统计计算评估的可靠性和观察者间一致性系数。用免疫组化染色(CD20、CD3、Bcl2)确认解读结果。进行PCR分析IgH基因重排的克隆性。

结果

小B细胞NHL和慢性淋巴结炎形态学评估的观察者间一致性显示卡方系数为0.69,属于高度一致类别。根据形态学和免疫组化结果将病例分为3组;淋巴瘤组、反应性病变组和未确定组。PCR分析显示敏感性为90%,特异性为60%。

结论

本研究显示病理学家在小B细胞NHL诊断方面具有高度一致性。对于疑难病例,PCR作为形态学和免疫组化检查的补充方法有助于确立明确诊断。

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