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Pax-2作为细胞病理学中肾细胞癌免疫组化标志物的效用。

The utility of Pax-2 as an immunohistochemical marker for renal cell carcinoma in cytopathology.

作者信息

Gokden Neriman, Kemp Susan A, Gokden Murat

机构信息

Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.

出版信息

Diagn Cytopathol. 2008 Jul;36(7):473-7. doi: 10.1002/dc.20842.

Abstract

Pax-2 is a homeogene expressed during kidney development. Its expression in renal cell carcinoma (RCC) has been previously evaluated in histologic samples with a high sensitivity and specificity. Here, we investigated the utility of Pax-2 immunohistochemistry (IHC) for RCC in cytologic material, in comparison with a variety of other neoplasms. Pax-2 IHC was performed on cell block sections of 33 RCCs (14 primary, 19 metastatic) and 35 non-RCC malignancies, including 26 carcinomas, five mesenchymal tumors, one neuroblastoma, two melanomas, and one lymphoma, from fine-needle aspirations and body fluids. The presence or absence of nuclear staining and its intensity and distribution in positive cases were evaluated. Of 33 RCCs, Pax-2 was positive in 20 (61%) and negative in 13 (39%). All staining was nuclear, with an admixture of weakly or strongly staining nuclei. Only an endometrial adenocarcinoma was positive in the non-RCC group. The sensitivity and specificity of Pax-2 IHC for RCC were 61 and 97%, respectively. Pax-2 is a moderately sensitive and highly specific marker for RCC in cytologic material, with a lower sensitivity compared with tissue sections, likely due to a patchy expression pattern, and should be included in the immunohistochemical work-up of malignancies.

摘要

Pax-2是一种在肾脏发育过程中表达的同源基因。此前已在组织学样本中对其在肾细胞癌(RCC)中的表达进行了评估,具有较高的敏感性和特异性。在此,我们研究了Pax-2免疫组织化学(IHC)在细胞学材料中对RCC的应用价值,并与多种其他肿瘤进行了比较。对33例RCC(14例原发性,19例转移性)以及35例非RCC恶性肿瘤(包括26例癌、5例间叶组织肿瘤、1例神经母细胞瘤、2例黑色素瘤和1例淋巴瘤)的细针穿刺和体液的细胞块切片进行了Pax-2 IHC检测。评估了阳性病例中核染色的有无及其强度和分布情况。在33例RCC中,Pax-2阳性20例(61%),阴性13例(39%)。所有染色均为核染色,核染色有弱染或强染混合情况。非RCC组中只有1例子宫内膜腺癌呈阳性。Pax-2 IHC对RCC的敏感性和特异性分别为61%和97%。Pax-2是细胞学材料中RCC的一种中度敏感且高度特异的标志物,与组织切片相比敏感性较低,可能是由于其呈斑片状表达模式,应纳入恶性肿瘤的免疫组织化学检查中。

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