Renal oncocytoma with and without intravascular extension into the branches of renal vein have the same morphological, immunohistochemical, and genetic features

被引:19
作者
Hes, Ondrej [1 ,2 ,3 ]
Michal, Michal [3 ]
Sima, Radek [3 ]
Vanecek, Tomas [3 ]
Brunelli, Matteo [4 ]
Martignoni, Guido [4 ]
Kuroda, Naoto [5 ]
Alvarado Cabrero, Isabel [6 ]
Perez-Montiel, Delia [7 ]
Hora, Milan [8 ]
Uerge, Tomas [8 ]
Dvorak, Miroslav [9 ]
Jarosova, Marie [10 ]
Yang, Ximing [11 ]
机构
[1] Fac Med, Lab Spec Diagnost, Dept Pathol, Plzen 32318, Czech Republic
[2] Univ Hosp, Plzen 32318, Czech Republic
[3] Charles Univ Prague, Hosp Plzen, Dept Pathol, Plzen, Czech Republic
[4] Univ Verona, Dept Pathol, I-37100 Verona, Italy
[5] Red Cross Hosp Kochi, Dept Pathol, Kochi, Japan
[6] Ctr Med Mexico City, Dept Pathol, Mexico City, DF, Mexico
[7] Inst Nacl Cancerol, Dept Pathol, Mexico City, DF, Mexico
[8] Charles Univ Prague, Hosp Plzen, Dept Urol, Plzen, Czech Republic
[9] Charles Univ Prague, Dept Forens Med, Plzen, Czech Republic
[10] Univ Hosp Olomouc, Dept Hematooncol, Olomouc, Czech Republic
[11] Northwestern Univ, Feinberg Sch Med, Dept Pathol, Chicago, IL 60611 USA
关键词
kidney; renal oncocytoma; intravascular; intravenous extension; molecular biology;
D O I
10.1007/s00428-007-0541-1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We attempted to investigate the clinicopathological correlation of renal oncocytoma (RO) with renal vein extension. We identified seven ROs with extension into the branches of renal vein. The age of seven patients ranged from 61 to 82 years. Five cases were identified incidentally; two patients had gross hematuria. After surgery, all patients were alive and free of tumors with follow-up of 1 to 5 years (mean=3.6). Oncocytomas measured from 2.2 to 7.5 cm. Renal vein extension was grossly suspected in five of seven cases and histologically confirmed in all seven cases. Tumor cells were positive for cytokeratins, mitochondrial-antigen (MIA), epithelial membrane antigen (EMA), and parvalbumin; five of seven tumors were focally positive for CD117. Ultrastructurally, the cytoplasm was packed by mitochondria. Molecular genetic analysis did not detect abnormal numbers of chromosomes 1, 2, 6, 7, 10, 17, and XY by fluorescence in situ hybridization, loss of heterozygosity on 3p and mutation of von Hippel-Lindau gene in all cases. Array comparative genomic hybridization analysis of two cases did not show any major genetic changes. Our conclusions are as follows: (1) renal oncocytomas may have intravascular extension to the branches of the renal vein; (2) renal oncocytomas with intravascular extension to the branches of the renal vein have the same morphological, immunohistochemical, and cytogenetic findings as have their counterparts without evidence of intravascular invasion; (3) the absence of metastases suggests an overall benign behavior of this tumor, but this has to be substantiated by further studies with a long-term follow-up; and (4) in a renal tumor with granular cytoplasm showing renal vein extension, it is necessary to carefully exclude renal cell carcinomas such as chromophobe RCC, oncocytic variant of papillary RCC, and granular variant of clear cell RCC.
引用
收藏
页码:193 / 200
页数:8
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