نتایج جستجو برای: lindau disease

تعداد نتایج: 1491542  

Journal: :Internal medicine 1984
N Mizuno S Naruse M Kitagawa H Ishiguro Y Nakae H Ieda N Iizuka O Ito Y Seki S B Ko T Yoshikawa T Hayakawa T Sano J Kamiya Y Nimura T Nagasaka

We describe a 42-year-old man with von Hippel-Lindau disease and islet cell tumor of the pancreas. He had retinal and cerebellar hemangioblastomas. His sister had pheochromocytoma. A pancreatic tumor was detected by ultrasonography at his periodical medical checkup. Contrast enhanced computed tomography and abdominal angiography revealed a hypervascular tumor in the pancreatic head. Histologica...

2017
Xu-Ting Zhi Qi-Yu Bo Feng Zhao Dong Sun Tao Li

RATIONALE Von Hippel-Lindau (VHL) disease is a rare inherited, autosomal-dominant syndrome caused by heterozygous germline mutations in the VHL gene. VHL patients are prone to develop benign and malignant tumors and cysts in multiple organ systems involving kidneys, pancreas and central nervous system (CNS). The varied and complex clinical manifestations and radiological findings of VHL are of ...

2017
Shuanghe Peng Matthew J. Shepard Jiangyi Wang Teng Li Xianghui Ning Lin Cai Zhengping Zhuang Kan Gong

von Hippel-Lindau (VHL) disease is caused by mutations in the VHL gene and demonstrates marked phenotypic variability. Genotype-phenotype correlations in Chinese VHL patients have been unclear. To establish genotype-phenotype correlations in Chinese VHL patients, we collected VHL mutations and phenotypes of 291 patients with VHL disease from 115 unrelated families. Genotype-phenotype correlatio...

Journal: :Investigative ophthalmology & visual science 2000
M Niemelä S Lemeta M Sainio S Rauma E Pukkala J Kere T Böhling L Laatikainen J Jääskeläinen P Summanen

PURPOSE To assess the prevalence of von Hippel-Lindau (VHL) disease and prognosis of vision in patients with retinal hemangioblastomas (HBs). METHODS Thirty-six consecutive patients with retinal HBs were treated at Helsinki University Hospital between 1974 and 1998. Detailed neurologic, ophthalmologic, and radiologic examinations; pedigree; mutation analyses; and collection of all relevant cl...

Journal: :Oncology research and treatment 2014
Sabine Schmid Silke Gillessen Isabelle Binet Michael Brändle Daniel Engeler Jeannette Greiner Claudia Hader Karl Heinimann Patrik Kloos Willy Krek Ina Krull Sandro J Stoeckli Michael C Sulz Karin van Leyen Johannes Weber Christian Rothermundt Thomas Hundsberger

Von Hippel-Lindau (VHL) disease is an autosomal dominantly inherited tumour predisposition syndrome with an incidence of 1:36,000 newborns, the estimated prevalence in Europe is about 1-9/100,000. It is associated with an increased risk of developing various benign and malignant tumours, thus affecting multiple organs at different time points in the life of a patient. Disease severity and diver...

Journal: :The Journal of the Japanese Association for Chest Surgery 2010

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