Hereditary Papillary Renal Carcinoma: Pathology and Pathogenesis

Author(s):  
L. Schmidt ◽  
I. Lubensky ◽  
W.M. Linehan ◽  
B. Zbar
2012 ◽  
Vol 11 (3) ◽  
pp. 535-537 ◽  
Author(s):  
Karin A. W. Wadt ◽  
Anne-Marie Gerdes ◽  
Thomas V. O. Hansen ◽  
Birgitte G. Toft ◽  
Lennart Friis-Hansen ◽  
...  

2004 ◽  
Vol 172 (4 Part 1) ◽  
pp. 1256-1261 ◽  
Author(s):  
LAURA S. SCHMIDT ◽  
MICHAEL L. NICKERSON ◽  
DEBORA ANGELONI ◽  
GLADYS M. GLENN ◽  
McCLELLAN M. WALTHER ◽  
...  

2004 ◽  
Vol 4 (8) ◽  
pp. 855-868 ◽  
Author(s):  
Pathirage Dharmawardana ◽  
Alessio Giubellino ◽  
Donald Bottaro

2006 ◽  
Vol 164 (2) ◽  
pp. 142-147 ◽  
Author(s):  
Esther Prat ◽  
Marta Bernués ◽  
Javier del Rey ◽  
Jordi Camps ◽  
Immaculada Ponsa ◽  
...  

Author(s):  
Claudia E. Rübe ◽  
Bernadine R. Donahue ◽  
Jay S. Cooper ◽  
Caspian Oliai ◽  
Yan Yu ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-11 ◽  
Author(s):  
Glen W. Barrisford ◽  
Eric A. Singer ◽  
Inger L. Rosner ◽  
W. Marston Linehan ◽  
Gennady Bratslavsky

Familial renal cancer (FRC) is a heterogeneous disorder comprised of a variety of subtypes. Each subtype is known to have unique histologic features, genetic alterations, and response to therapy. Through the study of families affected by hereditary forms of kidney cancer, insights into the genetic basis of this disease have been identified. This has resulted in the elucidation of a number of kidney cancer gene pathways. Study of these pathways has led to the development of novel targeted molecular treatments for patients affected by systemic disease. As a result, the treatments for families affected by von Hippel-Lindau (VHL), hereditary papillary renal carcinoma (HPRC), hereditary leiomyomatosis renal cell carcinoma (HLRCC), and Birt-Hogg-Dubé (BHD) are rapidly changing. We review the genetics and contemporary surgical management of familial forms of kidney cancer.


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