We report herein a case of cerebellar hemangioblastoma complicated by pregnancy and concerns about the period in which surgery could be performed successfully. A 19-year-old woman, who was also 35 weeks pregnant, was admitted to our hospital with headache, nausea, and general fatigue. Neurological examination on admission revealed disturbed consciousness, and the patient's general condition was...

We report a very rare case of hemangioblastomatosis that developed after surgical removal of a solitary cerebellar hemangioblastoma (HB). A 51-yr-old man presented with back pain 10 yr after undergoing surgery for cerebellar HB. Magnetic resonance imaging showed numerous mass lesions along the entire neuraxis accompanied by prominent leptomeningeal enhancement. Genomic DNA analysis showed no mu...

CASE The patient is a 37 year-old female who was diagnosed with Von Hippel-Lindau disease at the age of 28 years. At presentation the patient had an abdominal sonogram showing pancreatic cysts and a single liver hemangioma, normal ophthalmologic examination and normal CT scan of the brain. One year later, she had an episode of vertigo and severe headache and a new CT scan of the brain showed an...

Abstract Von Hippel-Lindau disease is an autosomal dominant disorder characterized by development of variety benign and malignant tumors cysts including brain stem, cerebellum, spinal cord as well pancreas, kidneys, retina. The most common associated with the are hemangioblastomas. Symptomatic CNS hemangioblastomas maybe first presentation disease. Initial during pregnancy uncommon presents uni...