Hemangioblastoma
Hemangioblastoma is a rare, benign tumor of the central nervous system that originates from the vascular system, usually in the cerebellum, brainstem or spinal cord. This tumor is most commonly found in adults aged 20-50 years. Hemangioblastomas are associated with Von Hippel-Lindau disease, a genetic disorder that leads to the development of multiple tumors.
Symptoms[edit | edit source]
The symptoms of hemangioblastoma can vary depending on the location of the tumor. Common symptoms include headache, nausea, vomiting, ataxia (lack of muscle coordination), vertigo (dizziness), and nystagmus (involuntary eye movement). In some cases, hemangioblastomas can cause hydrocephalus (accumulation of fluid in the brain), leading to increased intracranial pressure.
Diagnosis[edit | edit source]
Diagnosis of hemangioblastoma is typically made through magnetic resonance imaging (MRI) or computed tomography (CT) scans. These imaging tests can reveal the presence and location of the tumor. In some cases, a biopsy may be performed to confirm the diagnosis.
Treatment[edit | edit source]
Treatment for hemangioblastoma usually involves surgical removal of the tumor. In cases where surgery is not possible, radiation therapy may be used. The prognosis for patients with hemangioblastoma is generally good, as these tumors are benign and slow-growing. However, they can cause serious complications if they are not treated.
See also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD