| Hemangioblastoma | |
|---|---|
| Classification and external resources | |
Micrograph of a cerebellar hemangioblastoma. HPS stain. |
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| ICD-O: | M9161/1 |
| DiseasesDB | 31512 |
| eMedicine | med/2991 radio/326 |
| MeSH | D018325 |
Hemangioblastomas (also known as capilliary hemangioblastomas[1]) are tumors of the central nervous system that originate from the vascular system usually during middle-age. Sometimes these tumors occur in other sites such as the spinal cord and retina.[2] They may be associated with other diseases such as polycythemia (increased blood cell count), pancreatic cysts and Von Hippel-Lindau syndrome (VHL syndrome). Hemangioblastomas are most commonly composed of stromal cells in small blood vessels and usually occur in the cerebellum, brain stem or spinal cord. They are classed as grade one tumors under the World Health Organisation's classification system.[1]
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The primary diagnosis is made with a computed tomography scan (CT scan). On a scan, hemangioblastoma shows as a well-defined, black region in the cerebellum with a white nodule on the wall. Sometimes multiple lesions are present.[2]
The treatment for hemangioblastoma is surgical excision of the tumour. Although usually straightforward to carry out, recurrence of the tumor or more tumors at a different site develop in approximately 20% of patients.[2] Gamma Knife Radiosurgery as well as LINAC have also been employed to successfully treat recurrence and control tumor growth of cerebellar hemangioblastomas.
The outcome for hemangioblastoma is very good, if surgical extraction of the tumor can be achieved; excision is possible in most cases and permanent neurologic deficit is uncommon and can be avoided altogether if the tumor is diagnosed and treated early. Persons with VHL syndrome have a bleaker prognosis than those who have sporadic tumors since those with VHL syndrome usually have more than one lesion.[1]
Hemangioblastomas can cause polycythemia.
Hemangioblastomas usually occur in adults, yet tumors may appear in VHL syndrome at much younger ages. Men and women are approximately at the same risk. Although they can occur in any section of the central nervous system, they usually occur in either side of the cerebellum, the brain stem or the spinal cord.[1]