Pigmented microcystic chromophobe renal cell carcinoma

被引:15
作者
Dundr, Pavel
Pesl, Michael
Povysil, Ctibor
Tvrdik, Daniel
Pavlik, Ivan
Soukup, Viktor
Dvoracek, Jan
机构
[1] Charles Univ Prague, Inst Pathol, Fac Med 1, Prague 12800, Czech Republic
[2] Charles Univ Prague, Gen Fac Hosp, Prague 12800, Czech Republic
[3] Charles Univ Prague, Dept Urol, Fac Med 1, Prague 12800, Czech Republic
关键词
kidney; chromophobe renal cell carcinoma; pigmented; microcystic;
D O I
10.1016/j.prp.2007.05.005
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We report a case of a 60-year-old female with a pigmented microcystic chromophobe renal cell carcinoma (PMCRCC). The tumor was 4.5 cm in diameter, and was located in the right kidney. Grossly, on cross section, the tumor was light gray with multiple small brown to black pigmented foci up to 0.2 cm in diameter. Histologically, the tumor showed a microcystic arrangement with cribriform areas and formation of adenomatous structures. The microcystic and cribriform areas were composed of larger pale cells and smaller eosinophilic cells, with cytological features of conventional chromophobe renal cell carcinoma (CRCC). The cytological features of the cells within the adenomatous structures were different. These cells were mostly columnar with nuclei at the base, and had a variable amount of pale to eosinophilic cytoplasm. There were foci of ample brown pigmentation located in the cytoplasm of the tumor cells and extracellularly. In addition, microscopic calcifications were present. Immunohistochemically, the tumor cells were positive for EMA, E-cadherin, cytokeratin CAM5.2, and cytokeratin AE1/AE3. Cytokeratin 7 was positive only focally. S-100 protein, melan A, HMB 45, vimentin, and CD117 were negative. PMCRCC is a rare tumor. To the best of our knowledge, only one series containing 20 cases of this variant of CRCC has been described to date. The important feature is that PMCRCC seems to have a relatively benign biological behavior, and distant metastases and sarcomatoid transformation are absent. (c) 2007 Elsevier GmbH. All rights reserved.
引用
收藏
页码:593 / 597
页数:5
相关论文
共 23 条
[1]   Sarcomatoid renal cell carcinoma: The chromophobe connection [J].
Akhtar, M ;
Tulbah, A ;
Kardar, AH ;
Ali, MA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (10) :1188-1195
[2]  
BONSIB SM, 1996, J UROL PATHOL, V4, P9
[3]  
CochandPriollet B, 1997, ARCH PATHOL LAB MED, V121, P1081
[4]   CHROMOPHOBE CELL RENAL-CARCINOMA - CLINICOPATHOLOGICAL FEATURES OF 50 CASES [J].
CROTTY, TB ;
FARROW, GM ;
LIEBER, MM .
JOURNAL OF UROLOGY, 1995, 154 (03) :964-967
[5]  
FUKUDA T, 1997, HISTOPATHOLOGY, V25, P38
[6]  
Gong Yun, 2003, Arch Pathol Lab Med, V127, pe38
[7]   Survival in patients with rare subtypes of renal cell carcinoma [J].
Grabowski, M ;
Huzarski, T ;
Lubinski, J ;
Sikorski, A .
BJU INTERNATIONAL, 2002, 89 (06) :599-600
[8]   Chromophobe renal cell carcinoma with microcystic and adenomatous arrangement and pigmentation - a diagnostic pitfall. Morphological, immunohistochemical, ultrastructural and molecular genetic report of 20 cases [J].
Hes, O ;
Vanecek, T ;
Perez-Montiel, DM ;
Cabrero, IA ;
Hora, M ;
Suster, S ;
Lamovec, J ;
Curik, R ;
Mandys, V ;
Michal, M .
VIRCHOWS ARCHIV, 2005, 446 (04) :383-393
[9]   PIGMENTED RENAL-CELL CARCINOMA [J].
KAMISHIMA, T ;
FUKUDA, T ;
EMURA, I ;
TANIGAWA, T ;
NAITO, M .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1995, 19 (03) :350-356
[10]  
Kovacs G, 1997, J PATHOL, V183, P131, DOI 10.1002/(SICI)1096-9896(199710)183:2<131::AID-PATH931>3.0.CO