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Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions
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, immunohistoc...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019899/ https://www.ncbi.nlm.nih.gov/pubmed/29963177 http://dx.doi.org/10.3892/ol.2018.8752 |
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author | Wang, Yiqiu Ding, Ying Wang, Jian Gu, Min Wang, Zengjun Qin, Chao Han, Conghui Li, Hongxia Liu, Xia Wu, Pengfei Li, Guangchao |
author_facet | Wang, Yiqiu Ding, Ying Wang, Jian Gu, Min Wang, Zengjun Qin, Chao Han, Conghui Li, Hongxia Liu, Xia Wu, Pengfei Li, Guangchao |
author_sort | Wang, Yiqiu |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6019899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-60198992018-06-29 Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions Wang, Yiqiu Ding, Ying Wang, Jian Gu, Min Wang, Zengjun Qin, Chao Han, Conghui Li, Hongxia Liu, Xia Wu, Pengfei Li, Guangchao Oncol Lett Articles 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. D.A. Spandidos 2018-07 2018-05-21 /pmc/articles/PMC6019899/ /pubmed/29963177 http://dx.doi.org/10.3892/ol.2018.8752 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Wang, Yiqiu Ding, Ying Wang, Jian Gu, Min Wang, Zengjun Qin, Chao Han, Conghui Li, Hongxia Liu, Xia Wu, Pengfei Li, Guangchao Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions |
title | Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions |
title_full | Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions |
title_fullStr | Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions |
title_full_unstemmed | Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions |
title_short | Clinical features and survival analysis of clear cell papillary renal cell carcinoma: A 10-year retrospective study from two institutions |
title_sort | clinical features and survival analysis of clear cell papillary renal cell carcinoma: a 10-year retrospective study from two institutions |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019899/ https://www.ncbi.nlm.nih.gov/pubmed/29963177 http://dx.doi.org/10.3892/ol.2018.8752 |
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