Abstract
von Hippel-Lindau (VHL) disease is an autosomaldominant disorder characterized by cysts andcystadenoma in the kidney, pancreas andepididymis and angiomas of the central nervoussystem and retina as well as renal cellcarcinoma (RCC), phaeochromocytoma, islettumors of the pancreas, and endolympatic sactumors. VHL for its multicentric-characteristicand bilateralism often puts the surgeon inchallenging situation. We present a case of VHLwith bilateral RCC and retinal angiomas managedwith right radical nephrectomy and left repeatpartial nephrectomy.
Similar content being viewed by others
References
Hes FJ, Slootweg PJ, van Vroonhoven TJ, Hene RJ, Feldberg MA, Zewald RA, Ploos van Amstel JK, Hoppener JW, Pearson PL, Lips CJ. Management of renal cell carcinoma in von Hippel-Lindau disease. Eur J Clin Invest 1999 Jan; 29(6): 68–75.
Nanri M, Uda M, Iguchi Y, Gouya N, Toma H, Kihara T. A case of renal cell carcinoma associated with von Hippel-Lindau disease and the necessity for family genetic diagnosis. Hinyokika Kiyo 1999 Nov; 45(11): 755–758.
Hretien Y, Chauveau D, Richard S, Droz D, Correas JM, Mejean A, Dufour B, Grunfeld JP. Treatment of von Hippel-Lindau disease with renal involvement. Prog Urol 1997 Dec; 7(6): 939–947.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Ansari, M., Gupta, N. & Kumar, P. von Hippel-Lindau disease with bilateral multiple renal cell carcinoma managed by right radical nephrectomy and left repeat partial nephrectomy. Int Urol Nephrol 35, 471–473 (2003). https://doi.org/10.1023/B:UROL.0000025633.40416.57
Issue Date:
DOI: https://doi.org/10.1023/B:UROL.0000025633.40416.57