Literature DB >> 11705642

Clinical management of Von Hippel-Lindau (VHL) disease.

F J Hes1, R B van der Luijt, C J Lips.   

Abstract

Von Hippel-Lindau (VHL) disease is an autosomal, dominant inherited tumour syndrome with an estimated prevalence of 2-3 per 100,000 persons. A germline mutation in the VHL gene predisposes carriers to tumours in multiple organs. These tumours may include haemangioblastoma in the retina and central nervous system (CNS), renal cell carcinoma, phaeochromocytoma, islet cell tumours of the pancreas, and endolymphatic sac tumours, as well as cysts and cystadenoma in the kidney, pancreas, epididymis and broad ligament. Penetrance of VHL disease is high, most carriers of a VHL germline mutation develop one or more tumours by the age of 60 years. The most common symptoms include: loss of vision, raised intracranial pressure, neurological deficits, paroxysmal raised blood pressure and local pain. At present, metastases from renal cell carcinoma and neurological complications from cerebellar haemangioblastoma are the most common causes of death. However, it is anticipated that intensive radiological and clinical monitoring, and advanced operation techniques will reduce both morbidity and mortality in patients with VHL disease.

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Year:  2001        PMID: 11705642     DOI: 10.1016/s0300-2977(01)00165-6

Source DB:  PubMed          Journal:  Neth J Med        ISSN: 0300-2977            Impact factor:   1.422


  11 in total

1.  Identification of membrane type-1 matrix metalloproteinase as a target of hypoxia-inducible factor-2 alpha in von Hippel-Lindau renal cell carcinoma.

Authors:  Brenda L Petrella; Jouko Lohi; Constance E Brinckerhoff
Journal:  Oncogene       Date:  2005-02-03       Impact factor: 9.867

2.  Pazopanib therapy for cerebellar hemangioblastomas in von Hippel-Lindau disease: case report.

Authors:  Betty Y S Kim; Eric Jonasch; Ian E McCutcheon
Journal:  Target Oncol       Date:  2012-02-29       Impact factor: 4.493

3.  Inactivation of the arylhydrocarbon receptor nuclear translocator (Arnt) suppresses von Hippel-Lindau disease-associated vascular tumors in mice.

Authors:  Erinn B Rankin; Debra F Higgins; Jacqueline A Walisser; Randall S Johnson; Christopher A Bradfield; Volker H Haase
Journal:  Mol Cell Biol       Date:  2005-04       Impact factor: 4.272

4.  Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort.

Authors:  Juliann M Savatt; Nicole M Ortiz; Gretchen M Thone; Whitney S McDonald; Melissa A Kelly; Alexander S F Berry; Madiha M Alvi; Miranda L G Hallquist; Jennifer Malinowski; Nicholas C Purdy; Marc S Williams; Amy C Sturm; Adam H Buchanan
Journal:  BMC Med       Date:  2022-06-07       Impact factor: 11.150

Review 5.  Familial syndromes associated with intracranial tumours: a review.

Authors:  Adrianna M Ranger; Yatri K Patel; Navjot Chaudhary; Ram V Anantha
Journal:  Childs Nerv Syst       Date:  2013-11-06       Impact factor: 1.475

6.  Von Hippel-Lindau disease: an evaluation of natural history and functional disability.

Authors:  Alberto Feletti; Mariagiulia Anglani; Bruno Scarpa; Francesca Schiavi; Francesca Boaretto; Stefania Zovato; Elisa Taschin; Mario Gardi; Elisabetta Zanoletti; Stefano Piermarocchi; Alessandra Murgia; Giacomo Pavesi; Giuseppe Opocher
Journal:  Neuro Oncol       Date:  2016-01-12       Impact factor: 12.300

7.  Tumor cell invasion of von Hippel Lindau renal cell carcinoma cells is mediated by membrane type-1 matrix metalloproteinase.

Authors:  Brenda L Petrella; Constance E Brinckerhoff
Journal:  Mol Cancer       Date:  2006-12-01       Impact factor: 27.401

8.  Hemangioblastoma of the Central Nervous System: A Case Series of Patients Surgically Treated at Shohada-e-Tajrish Hospital, Tehran, Iran during 2004-2014.

Authors:  Mahsa Ahadi; Hanieh Zham; Azadeh Rakhshan; Mitra Rafizadeh; Davood Talebi Bayazi; Masoud Baikpour; Afshin Moradi
Journal:  Iran J Child Neurol       Date:  2019

9.  Intra-Familial Phenotypic Heterogeneity and Telomere Abnormality in von Hippel- Lindau Disease: Implications for Personalized Surveillance Plan and Pathogenesis of VHL-Associated Tumors.

Authors:  Jiangyi Wang; Xiang Peng; Cen Chen; Xianghui Ning; Shuanghe Peng; Teng Li; Shengjie Liu; Baoan Hong; Jingcheng Zhou; Kaifang Ma; Lin Cai; Kan Gong
Journal:  Front Genet       Date:  2019-04-24       Impact factor: 4.599

10.  A patient with bilateral pheochromocytoma as part of a Von Hippel-Lindau (VHL) syndrome type 2C.

Authors:  Jennifer M J Schreinemakers; Bernard A Zonnenberg; Jo W M Höppener; Frederik J Hes; Inne H M Borel Rinkes Rinkes; Cornelis J M Lips
Journal:  World J Surg Oncol       Date:  2007-10-08       Impact factor: 2.754

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