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

被引:25
|
作者
Wang, Yiqiu [1 ,2 ]
Ding, Ying [3 ]
Wang, Jian [4 ]
Gu, Min [1 ]
Wang, Zengjun [1 ]
Qin, Chao [1 ]
Han, Conghui [5 ]
Li, Hongxia [3 ]
Liu, Xia [6 ]
Wu, Pengfei [7 ]
Li, Guangchao [8 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Urol, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Southeast Univ, Coll Med, Affiliated Xuzhou Hosp, Dept Surg Oncol, Xuzhou 221009, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 1, Dept Pathol, Nanjing 210029, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Affiliated Hosp 1, Dept Oncol, Nanjing 210029, Jiangsu, Peoples R China
[5] Southeast Univ, Coll Med, Affiliated Xuzhou Hosp, Dept Urol, Xuzhou 221009, Jiangsu, Peoples R China
[6] Southeast Univ, Coll Med, Affiliated Xuzhou Hosp, Dept Pathol, Xuzhou 221009, Jiangsu, Peoples R China
[7] Nanjing Med Univ, Affiliated Hosp 1, Dept Radiol, Nanjing 210029, Jiangsu, Peoples R China
[8] Southeast Univ, Coll Med, Affiliated Xuzhou Hosp, Dept Radiol, Xuzhou 221009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
clear cell papillary renal cell carcinoma; clinical features; survival analysis; SINGLE INSTITUTION; KIDNEY-DISEASE; DISTINCT; CANCER; TUMOR; EMPHASIS; OBESITY; RISK; CLASSIFICATION; HYBRIDIZATION;
D O I
10.3892/ol.2018.8752
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
引用
收藏
页码:1010 / 1022
页数:13
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