Abstract
Purpose
Types 1 and 2 by Delahunt of papillary renal cell carcinoma (PRCC) are traditionally differentiated. An oncocytic variant of PRCC (O-PRCC) has recently been described. We compare clinical data of O-PRCC with other subtypes of PRCC such as the main tumour size, necrotic changes, presence of pseudocapsula and real extrarenal growth in retrospective study.
Methods
From 1/1992 to 10/2009, 1,398 patients with 1,436 renal tumours were surgically treated in our institution. PRCCs were described in 109 (7.6%). Among PRCC, O-PRCCs were in 12 (11%), PRCC type 1 in 86 (78.9%), PRCC type 2 in 8 (7.3%) and others in 3 (2.8%) cases.
Results
The patient’s mean age with O-PRCC (M:F ratio = 2:1) was 67.5 ± 10.9 versus 63.5 ± 14.1 in type 1 and 57.9 ± 5.7 in type 2, the mean tumour size was 35 ± 12 mm versus 47 ± 22 and 37 ± 17, respectively. The follow-up of O-PRCC is 35.3 ± 12.3 months and all cases are without recurrence. We did not find any pseudocapsula in O-PRCC but it was a major sign of PRCC type 1 (32.6%). Huge microscopic necrotic changes were described in 33.3% of O-PRCC, in 33.7% of PRCC type 1 and 62.5% of PRCC type 2. Extrarenal growth was found only in 16.7% O-PRCC versus 40.7% in PRCC type I.
Conclusions
None of the O-PRCC had pseudocapsula and none had massive necroses in comparison of O-PRCC with PRCC types I and II. Extrarenal growth in O-PRCC is relatively rare. The malignant potential of O-PRCC is low.
Similar content being viewed by others
References
Mancilla-Jimenez R, Stanley RJ, Balth RA (1976) Papillary renal cell carcinoma. A clinical, radiological, and pathologic study of 34 cases. Cancer 38(6):2469–2480
Delahunt B, Eble JN (1997) Papillary renal cell carcinoma: a clinicopathologic and immunohistochemical study of 105 tumours. Mod Pathol 10:537–544
Young AN, Amin MB, Moreno CS, Lim SD, Cohen C, Petros JA, Marshall FF, Neish AS (2001) Expression profiling of renal epithelial neoplasms: a method for tumour classification and discovery of diagnostic molecular markers. Am J Pathol 158:1639–1651
Mejean A, Hopirtean V, Bazin JP, Larousserie F, Benoit H, Chreátien Y, Thiounn N, Dufour B (2003) Prognostic factors for the survival of patients with papillary renal cell carcinoma: meaning of histological typing and multifocality. J Urol 170:764–767
Yang XJ, Tan MH, Kim HL, Ditlev JA et al (2005) A molecular classification of papillary renal cell carcinoma. Cancer Res 65(13):5628–5637
Delahunt B, Eble JN, McCredie MR, Bethwaite PB, Stewart JH, Bilous AM (2001) Morphologic typing of papillary renal cell carcinoma: comparison of growth kinetics and patient survival in 66 cases. Hum Pathol 32:590–595
Yang F, Richter J, Schraml P, Bubendorf L, Gasser T, Kauter G, Mihatsch MJ, Moch H (1998) Chromosomal imbalances in papillary renal cell carcinoma: genetic differences between histological subtypes. Am J Pathol 153(5):1767–1773
Pignot G, Elie C, Cunquy S et al (2007) Survival analysis of 130 patients with papillary renal cell carcinoma: prognostic utility of type 1 and type 2 subclassification. Urology 69(2):230–235
Lefévre M, Couturier J, Sibony M, Bazille C, Boyer K, Callard P, Vieillefond A, Allory Y (2005) Adult papillary renal tumour with oncocytic cells: clinicopathologic, immunohistochemical, and cytogenetic features of 10 cases. Am J Surg Pathol 29(12):1576–1581
Hes O, Brunelli M, Michal M, Cossu Rocca P, Hora M, Chilosi M, Mina M, Boudova L, Menestrina F, Martignoni G (2006) Oncocytic papillary renal cell carcinoma: a clinicopathologic, immunohistochemical, ultrastructural, and interphase cytogenetic study of 12 cases. Ann Diagn Pathol 10(3):133–139
Kunju LP, Wonjo K, Wolf JS, Cheby L et al (2008) Papillary renal cell carcinoma with oncocytic cells and nonoverlapping low grade nuclei: expanding the morphologic spectrum with emphasis on clinicopathologic, immunohistochemical and molecular features. Hum Pathol 39:96–101
Park BH, Ro JY, Park WS et al (2009) Oncocytic papillary renal cell carcinoma with inverted nuclear pattern: distinct subtype with an indolent clinical course. Pathol Int 59:137–146
Mai KT, Kohler DM, Robertson SJ et al (2008) Oncocytic papillary renal cell carcinoma with solid architecture: mimic of renal oncocytoma. Pathol Int 58(3):164–168
Masuzawa N, Kishimoto M, Nishimura A, Shichiri Y, Yanagisawa A (2008) Oncocytic renal cell carcinoma having papillotubular growth: rare morphological variant of papillary renal cell carcinoma. Pathol Int 58:300–305
Hora M, Hes O, Reischig T, Ürge T, Klečka J, Ferda J, Michal M, Eret V (2008) Tumours in end-stage kidney. Transplant Proc 40(10):3354–3358
Hora M, Hes O, Klečka J, Boudová L, Chudáček Z, Kreuzberg B, Michal M (2004) Rupture of papillary renal cell carcinoma. Scan J Urol Nephrol 38(6):481–484
Schafter LR, Bach AM, Snyder ME, Kattan MW, Russo P (2006) The impact of tumour location on the histological subtype of renal cortical tumours. BJU Int 98:63–66
Hora M, Hes O, Ürge T, Klečka J, Eret V, Ferda J, Chudáček Z (2007) Papillary renal cell carcinoma are treated more frequently by laparoscopic partial nephrectomy due to their exophytic growth than non-papillary tumours. Eur Urol Suppl 6(2):236C
Ferda J, Hora M, Hes O, Ferdovaá E, Kreuzberg B (2007) Assessment of the kidney tumour vascular supply by two-phase MDCT-angiography. Eur J Radiol 62(2):295–301
Israel G, Bosniak M (2005) An update of the Bosniak renal cyst classification system. Urology 66:484–488
Acknowledgments
The work was supported by Czech government research project MSM 0021620819. 28th February 2010. Authors have not a financial relationship with the organisation that sponsored the research.
Conflict of interest statement
None.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Ürge, T., Hes, O., Ferda, J. et al. Typical signs of oncocytic papillary renal cell carcinoma in everyday clinical praxis. World J Urol 28, 513–517 (2010). https://doi.org/10.1007/s00345-010-0563-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00345-010-0563-1