Literature DB >> 19293973

Hereditary renal cell carcinoma associated with von Hippel-Lindau disease: a description of a Nova Scotia cohort.

Shannon Bradley1, Nadine Dumas, Mark Ludman, Lori Wood.   

Abstract

BACKGROUND: von Hippel-Lindau (VHL) disease is an autosomal dominant condition characterized by the development of benign and malignant tumours, including cases of renal cell carcinoma (RCC). Early detection of RCC through routine surveillance can lead to decreased morbidity and mortality. Data on the number of patients in Nova Scotia (NS) who have VHL disease, disease manifestations and the frequency and mode of the surveillance have not previously been collected or reported. This project was designed to obtain that information.
METHODS: The number and management of patients with VHL disease was determined by multiple sources: the Maritime Medical Genetics Service, patient charts, and pathology, radiology and laboratory data. The actual surveillance being performed was compared with that recommended in the literature.
RESULTS: Twenty-one patients from 11 families in NS were identified. Manifestations included cases of RCC (31.6%), central nervous system (CNS) hemangioblastoma (73.7%), retinal hemangioma (47.4%), renal cyst (47.4%) and pheochromocytoma (10.5%). Of the 6 patients with RCC, 4 had bilateral tumours, 2 required kidney transplants and 1 developed metastatic disease. Routine surveillance was being done for the CNS in 62.5% of patients, retina in 47.4%, abdomen in 43.8% and urine catecholamines in only 10.5%. Only 1 of the 6 patients who developed RCC was undergoing routine abdominal imaging. Surveillance investigations were ordered by a number of different specialists.
CONCLUSION: Patients with VHL disease in NS have a number of manifestations associated with their disease, including RCC, in a similar frequency to that reported in the literature. The surveillance of these patients is suboptimal in frequency and coordination. von Hippel-Lindau disease is a complex condition that requires a coordinated approach to care to ensure proper surveillance and treatment. Our study highlights current deficiencies and offers an enormous opportunity for improvement.

Entities:  

Year:  2009        PMID: 19293973      PMCID: PMC2645893          DOI: 10.5489/cuaj.1013

Source DB:  PubMed          Journal:  Can Urol Assoc J        ISSN: 1911-6470            Impact factor:   1.862


  14 in total

Review 1.  Role of VHL gene mutation in human cancer.

Authors:  William Y Kim; William G Kaelin
Journal:  J Clin Oncol       Date:  2004-12-15       Impact factor: 44.544

Review 2.  The von Hippel-Lindau tumor suppressor protein and clear cell renal carcinoma.

Authors:  William G Kaelin
Journal:  Clin Cancer Res       Date:  2007-01-15       Impact factor: 12.531

Review 3.  Von Hippel-Lindau disease: strategies in early detection (renal-, adrenal-, pancreatic masses).

Authors:  F J Hes; M A Feldberg
Journal:  Eur Radiol       Date:  1999       Impact factor: 5.315

Review 4.  Von Hippel-Lindau disease: gene to bedside.

Authors:  K B Sims
Journal:  Curr Opin Neurol       Date:  2001-12       Impact factor: 5.710

5.  Clinical features and natural history of von Hippel-Lindau disease.

Authors:  E R Maher; J R Yates; R Harries; C Benjamin; R Harris; A T Moore; M A Ferguson-Smith
Journal:  Q J Med       Date:  1990-11

6.  Identification of the von Hippel-Lindau disease tumor suppressor gene.

Authors:  F Latif; K Tory; J Gnarra; M Yao; F M Duh; M L Orcutt; T Stackhouse; I Kuzmin; W Modi; L Geil
Journal:  Science       Date:  1993-05-28       Impact factor: 47.728

Review 7.  Nephron-sparing surgery and renal transplantation in patients with renal cell carcinoma and von Hippel-Lindau disease.

Authors:  D A Goldfarb
Journal:  J Intern Med       Date:  1998-06       Impact factor: 8.989

Review 8.  Management of von Hippel-Lindau-associated kidney cancer.

Authors:  Robert L Grubb; Peter L Choyke; Peter A Pinto; W Marston Linehan; McClellan M Walther
Journal:  Nat Clin Pract Urol       Date:  2005-05

9.  A rational approach to radiological screening in von Hippel-Lindau disease.

Authors:  R W Harries
Journal:  J Med Screen       Date:  1994-04       Impact factor: 2.136

10.  The natural history of renal lesions in von Hippel-Lindau disease: a serial CT study in 28 patients.

Authors:  P L Choyke; G M Glenn; M M Walther; B Zbar; G H Weiss; R B Alexander; W S Hayes; J P Long; K N Thakore; W M Linehan
Journal:  AJR Am J Roentgenol       Date:  1992-12       Impact factor: 3.959

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  4 in total

1.  Advanced renal cell carcinoma associated with von Hippel-Lindau disease: A case report and review of the literature.

Authors:  Lei Zhang; Bin Xu; Yiduo Wang; Chunhui Liu; Kai Lu; Yeqing Huang; Ning Liu; Xiaowen Zhang; Shuqiu Chen; Ming Chen
Journal:  Oncol Lett       Date:  2015-05-27       Impact factor: 2.967

2.  Canadian guideline on genetic screening for hereditary renal cell cancers.

Authors:  M Neil Reaume; Gail E Graham; Eva Tomiak; Suzanne Kamel-Reid; Michael A S Jewett; Georg A Bjarnason; Normand Blais; Melanie Care; Darryl Drachenberg; Craig Gedye; Ronald Grant; Daniel Y C Heng; Anil Kapoor; Christian Kollmannsberger; Jean-Baptiste Lattouf; Eamonn R Maher; Arnim Pause; Dean Ruether; Denis Soulieres; Simon Tanguay; Sandra Turcotte; Philippe D Violette; Lori Wood; Joan Basiuk; Stephen E Pautler
Journal:  Can Urol Assoc J       Date:  2013 Sep-Oct       Impact factor: 1.862

Review 3.  Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: not a needle in a haystack.

Authors:  João Castro-Teles; Bernardo Sousa-Pinto; Sandra Rebelo; Duarte Pignatelli
Journal:  Endocr Connect       Date:  2021-10-27       Impact factor: 3.335

4.  Knowledge of genetic testing for hereditary kidney cancer in Canada is lacking: The results of the Canadian national hereditary kidney cancer needs assessment survey.

Authors:  Philippe D Violette; Suzanne Kamel-Reid; Gail E Graham; M Neil Reaume; Michael A Jewett; Melanie Care; Joan Basiuk; Stephen E Pautler
Journal:  Can Urol Assoc J       Date:  2014-11       Impact factor: 1.862

  4 in total

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