نتایج جستجو برای: von hippel lindau syndrome

تعداد نتایج: 713978  

2014
Punit Sharma Varun Singh Dhull Chandrasekhar Bal Arun Malhotra Rakesh Kumar

Von Hippel-Lindau (VHL) syndrome is a rare neoplastic disorder characterized by central nervous system (CNS) and visceral tumors. We here present (68)Ga-labelled [1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid]-1-Nal3-Octreotide positron emission tomography computed tomography findings in a 52 year old female with VHL syndrome, demonstrating both CNS and visceral tumors.

1998
Andrew R Webster Richard B Fisher Lionel Ginsberg Eamonn R Maher

A probable diagnosis of von HippelLindau disease was made in a two generation family in which the proband had a phaeochromocytoma, renal cysts, and multiple cerebral cavernomas. His sister had multiple similar cerebral vascular lesions and his father died from renal carcinoma aged 42. Although the family did not satisfy the conventional diagnostic criteria for von Hippel-Lindau disease, an unde...

Journal: :Pediatric Neurology Briefs 1992

Journal: :Journal of Brain and Spine Foundation Nepal 2020

Journal: :Journal of Kidney Cancer and VHL 2017

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :Nephrology nursing journal : journal of the American Nephrology Nurses' Association 2007
Michele Inglese

Von Hippel-Lindau disease is a rare, familial disease consisting of multiple tumors, which can present in the eyes, brain, adrenal gland, pancreas, liver, spinal cord, kidneys, or other areas of the body. The renal tumors are primarily renal cell carcinoma. Renal involvement may be the primary manifestation, but most frequently it is a secondary manifestation. This article presents an overview ...

2017
Shimpei Maeda Fuyuhiko Motoi Shuhei Oana Kyohei Ariake Masamichi Mizuma Takanori Morikawa Hiroki Hayashi Kei Nakagawa Takashi Kamei Takeshi Naitoh Michiaki Unno

BACKGROUND von Hippel-Lindau disease is a dominantly inherited multi-system syndrome with neoplastic hallmarks. Pancreatic lesions associated with von Hippel-Lindau include serous cystic neoplasms, simple cysts, and neuroendocrine tumors. The combination of pancreatic neuroendocrine tumors and serous cystic neoplasms is relatively rare, and the surgical treatment of these lesions must consider ...

2017
Neha Varshney Amanuel A. Kebede Harry Owusu-Dapaah Jason Lather Manu Kaushik Jasneet S. Bhullar

Von Hippel-Lindau syndrome (VHL) is a familial neoplastic condition seen in approximately 1 in 36,000 live births. It is caused by germline mutations of the tumor suppressor gene VHL, located on the short arm of chromosome 3. While the majority of the affected individuals have a positive family history, up to 20% of cases arise from de novo mutations. VHL syndrome is characterized by the presen...

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