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Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions

机译:透明细胞乳头状肾细胞癌的临床特征和生存分析:来自两家机构的十年回顾性研究

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摘要

Clear cell papillary renal cell carcinoma (CCPRCC) is a recently recognized subtype of renal cell carcinoma entity, however, little is known about its clinical features. In the present study, 26 cases of CCPRCC were screened out from two institutions. The patient data, tissue pathology, immunohistochemical phenotype, computed tomographic images and survival analysis were studied. The mean age was 53.3 years and the average tumor size was 2.5 cm. A total of 17 patients' body mass indexes were higher than the normal level. A total of 11 patients had hypertension and 6 patients had a smoking history. Histopathologically, all cases of CCPRCC exhibited a tubular and papillary architecture, small to medium-sized cuboidal tumor cells with clear cytoplasms, and a low Fuhrman nuclear grade. All tumors were encapsulated by variably thick fibrous capsules. Immunohistochemistry showed diffuse and moderate to strong cytoplasmic staining for CK7, CA IX and vimentin, but negative for AMACR and CD10 (sometimes focally positive) in all cases. According to the results of Ki67 labeling index, the expression of Ki67 in CCPRCC was much lower than that in clear cell renal cell carcinoma (CCRCC) (2.19 vs. 7.07%, P<0.001) and that in papillary renal cell carcinoma (PRCC) (2.19 vs. 6.65%, P<0.001). Radiographically, the tumors were shown as small masses with smooth contour and mixed enhancement pattern. The multiphasic attenuation curve for CCPRCC, like that for CCRCC, increased in the corticomedullary phase markedly and decreased in the nephrographic phase and excretory phase gradually. At a median follow-up period of 50 months, no cancer-specific death or tumor recurrence was observed. Considering the favorable prognosis of CCPRCC, preoperative biopsy in order to make clear the diagnosis is particularly important. In light of the present findings, partial nephrectomy for patients with CCPRCC is recommended. If the patients cannot tolerate surgery, closed monitoring or radiofrequency ablation may be considered.
机译:透明细胞乳头状肾细胞癌(CCPRCC)是近来公认的肾细胞癌实体亚型,但对其临床特征知之甚少。在本研究中,从两个机构中筛选出26例CCPRCC病例。研究了患者数据,组织病理学,免疫组织化学表型,计算机断层扫描图像和生存分析。平均年龄为53.3岁,平均肿瘤大小为2.5厘米。共有17名患者的体重指数高于正常水平。共有11例患有高血压,6例有吸烟史。在组织病理学上,所有CCPRCC病例均显示为管状和乳头状结构,具有透明细胞质的中小型立方体肿瘤细胞和较低的Fuhrman核级。所有的肿瘤都被不同厚度的纤维囊包裹。免疫组织化学显示,CK7,CA IX和波形蛋白的细胞质呈弥漫性和中度至强度染色,但在所有情况下,AMACR和CD10均为阴性(有时为阳性)。根据Ki67标记指数的结果,CCPRCC中Ki67的表达远低于透明细胞肾细胞癌(CCRCC)(2.19 vs. 7.07%,P <0.001)和乳头状肾细胞癌(PRCC)。 (2.19 vs.6.65%,P <0.001)。影像学上,肿瘤显示为小肿块,轮廓光滑,混合增强模式。 CCPRCC的多相衰减曲线与CCRCC一样,在肾小管相中显着增加,而在肾病相和排泄相中则逐渐降低。在中位随访期为50个月时,未观察到癌症特异性死亡或肿瘤复发。考虑到CCPRCC的良好预后,术前活检以明确诊断尤为重要。根据目前的发现,建议对CCPRCC患者进行部分肾切除术。如果患者不能忍受手术,则可以考虑进行封闭监测或射频消融。

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