نتایج جستجو برای: cerebellar hemangioblastoma

تعداد نتایج: 27003  

Journal: :Journal of neurology, neurosurgery, and psychiatry 1989
C A Clelland C S Treip

Two cases of von Hippel-Lindau's disease with special reference to the occurrence of renal carcinoma are presented. The first case demonstrates the difficulty of differentiating cerebellar haemangioblastoma from metastatic renal carcinoma affecting the cerebellum. The valuable differentiating histological features were positive staining of metastatic renal carcinoma by antiepithelial membrane a...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1982
R V Jeffreys J A Napier S H Reynolds

Using an in vitro bioassay, erythropoiesis stimulating activity has been measured in serum, cyst fluids and tumour homogenates from fourteen patients with cerebellar haemangioblastoma. Only two patients had elevated peripheral blood red cell counts and haemoglobin concentrations. Significantly elevated serum erythropoiesis stimulating activity was found in only one patient. High level, however,...

Journal: :Journal of medical genetics 1990
E R Maher J R Yates M A Ferguson-Smith

Analysis of the age incidence curves for unilateral and bilateral retinoblastoma led Knudson to propose that hereditary tumours may arise by a single event and sporadic tumours by a two stage mutation process. It has been suggested recently that sporadic renal cell carcinoma may arise from a two stage mutation process. We analysed the age incidence curves for symptomatic renal cell carcinoma (n...

Journal: :Hormone research 2006
M Priesemann K M Davies L A Perry W M Drake S L Chew J P Monson M O Savage L B Johnston

Von Hippel-Lindau (VHL) is a rare autosomal dominant syndrome characterised by the association of retinal and CNS haemangioblastomas, phaeochromocytoma and renal cell carcinoma. If a child of an affected parent has inherited a VHL mutation or the parent's mutation cannot be identified, then clinical screening is recommended. We report the clinical features in three parent-offspring pairs where ...

2017
A. Cervio J. F. Villalonga R. Mormandi S. Condomí Alcorta G. Sevlever J. Salvat

BACKGROUND Hemangioblastomas (HBL) are uncommon tumors of the central nervous system (CNS), corresponding to 1-2.5% of all intracranial tumors. They can present sporadically or in patients with von Hippel-Lindau (VHL) disease and are most often located in the cerebellum, brainstem, and spinal cord. VHL disease is a multiple neoplasia syndrome inherited in an autosomal dominant fashion and cause...

2017
Yan Zhao Xin Jin Xiaomeng Gong Bingqin Guo Nan Li

Hemangioblastoma (HB) is an unusual benign, of uncertain histogenesis neoplasm predominantly affect adulthood. It typically occurs in the central nervous system (CNS), predominantly in the cerebellum, occasionally in the meninges, spinal cord, corpus callosum, lateral ventricle and pituitary gland. Besides, it occurs in peripheral nerves and extraneural tissues such as soft tissue, retroperiton...

Journal: :Neurosurgical Focus 2014

2015
Gun-Ill Lee Jae-Min Kim Kyu-Sun Choi Choong-Hyun Kim

Hemangioblastomas in the pituitary stalk are especially rare. Most pituitary stalk hemangioblastomas reported in the literature were associated with von Hippel-Lindau (VHL) disease. Here, we report only the 3rd case of sporadic pituitary stalk hemangioblastoma diagnosed in a 60-year-old woman. Despite the danger of potential complications due to excessive vascularity or proximity to important n...

Objectives: Cerebellar infarction is an ischemic type episode involving the three main cerebellar arteries. An infarction in each of these arteries causes different but common symptoms, requiring a particularly important contribution of physiotherapy to its treatment. This overview aimed to investigate the effectiveness of physiotherapy programs on the symptoms of patients with cerebellar infar...

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