用 p53 和波形蛋白双重免疫染色法区分高级别尿路上皮癌细胞和良性非典型细胞

Acta Cytologica Pub Date : 2024-05-21 DOI:10.1159/000539417
Hiroko Ose, Akihiro Nakamura, T. Nukaya, T. Sofue, Reiji Haba, Tomoo Itoh, Shingo Kamoshida, Hiroyuki Ohsaki
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引用次数: 0

摘要

导言:尿液细胞学检查是检测高级别尿路上皮癌(HGUC)不可或缺的检查方法;然而,如何区分HGUC细胞和形态相似的良性非典型细胞给临床带来了挑战。在本研究中,我们对 p53 和波形蛋白进行了双重免疫染色,以建立一种能准确区分 HGUC 细胞和良性非典型细胞的诊断方法:本研究包括41例经组织病理学或临床诊断的HGUC、11例尿路结石和22例肾小球疾病。从排空的尿液样本中制备尿液细胞学标本后,进行 p53 免疫染色,并计算 p53 阳性强度和 p53 阳性率。随后,对同一标本进行波形蛋白免疫染色,计算波形蛋白阳性率:结果:HGUC细胞组的平均p53阳性强度为2.40,平均p53阳性率为73.2%,平均波形蛋白阳性率为5.1%。相比之下,良性非典型细胞组的平均 p53 阳性强度、p53 阳性率和波形蛋白阳性率分别为 1.63%、36.7% 和 66.2%。两组在各项参数上均存在明显差异。此外,与单纯评估 p53 阳性强度、阳性率和波形蛋白阳性率相比,结合这三个参数结果的两个多重逻辑回归模型显示出更高的灵敏度和特异性:结论:p53 和波形蛋白双重免疫染色可将 HGUC 细胞与良性非典型细胞区分开来,因此可用于提高尿液细胞学诊断的准确性。
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p53 and vimentin double immunostaining to differentiate between high-grade urothelial carcinoma cells and benign atypical cells
Introduction: Urine cytology is an indispensable test for detecting high-grade urothelial carcinoma (HGUC); however, the distinction between HGUC cells and morphologically similar benign atypical cells poses clinical challenges. In this study, we performed double immunostaining for p53 and vimentin to establish a diagnostic method to accurately distinguish HGUC cells from benign atypical cells. Methods: This study included 41 cases of HGUC, 11 of urolithiasis, and 22 of glomerular disease diagnosed histopathologically or clinically. After preparing urine cytology specimens from voided urine samples, p53 immunostaining was performed, and the p53 positive intensity and p53 positivity rate were calculated. Subsequently, vimentin immunostaining was performed on the same specimens to calculate the rate of vimentin positivity. Results: The HGUC cell group had a mean p53 positive intensity of 2.40, a mean p53 positivity rate of 73.2%, and a mean vimentin positivity rate of 5.1%. In contrast, the mean p53 positive intensity, p53 positivity rate, and vimentin-positivity rate was 1.63, 36.7%, and 66.2%, respectively, in the benign atypical cell group. There were significant differences between the two groups for each parameter. Moreover, two multiple logistic regression models combining the results of these three parameters exhibited higher sensitivity and specificity than solely assessing the p53 positive intensity, positivity rate, and vimentin positivity rate. Conclusion: Since double immunostaining with p53 and vimentin distinguishes HGUC cells from benign atypical cells, it could be used to improve the diagnostic accuracy of urine cytology.
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p53 and vimentin double immunostaining to differentiate between high-grade urothelial carcinoma cells and benign atypical cells
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