Guidelines for surveillance of patients with von Hippel‐Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance

Von Hippel‐Lindau disease is a rare inherited cancer‐predisposition syndrome. The authors report the updated recommendations for the multiorgan surveillance protocols.

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Bibliographic Details
Published in	Cancer Vol. 129; no. 19; pp. 2927 - 2940
Main Authors	Daniels, Anthony B., Tirosh, Amit, Huntoon, Kristin, Mehta, Gautam U., Spiess, Philippe E., Friedman, Debra L., Waguespack, Steven G., Kilkelly, Jill E., Rednam, Surya, Pruthi, Sumit, Jonasch, Eric A., Baum, Laura, Chahoud, Jad
Format	Journal Article
Language	English
Published	United States Wiley Subscription Services, Inc 01.10.2023
Subjects	endolymphatic sac tumors Guidelines hemangioblastomas Kidney cancer Oncology Pancreatic cancer pancreatic neuroendocrine tumors pheochromocytoma renal cell cancer Surveillance Tumors VHL von Hipple‐Lindau syndrome kidney cancer pancreatic neuroendocrine tumors renal cell cancer pheochromocytoma hemangioblastomas VHL von Hipple-Lindau syndrome endolymphatic sac tumors
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ISSN	0008-543X 1097-0142 1097-0142
DOI	10.1002/cncr.34896

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Summary:	Von Hippel‐Lindau disease is a rare inherited cancer‐predisposition syndrome. The authors report the updated recommendations for the multiorgan surveillance protocols.
Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23
ISSN:	0008-543X 1097-0142 1097-0142
DOI:	10.1002/cncr.34896