Astrocytoma (patient information): Difference between revisions
No edit summary |
No edit summary |
||
Line 18: | Line 18: | ||
{{SI}} | {{SI}} | ||
'''Editor-in-Chief:''' Jinhui Wu, MD | '''Editor-in-Chief:'''{{CMG}}; Jinhui Wu, MD | ||
{{EJ}} | {{EJ}} |
Revision as of 13:47, 13 October 2009
For the WikiDoc page for this topic, click here
Template:DiseaseDisorder infobox
'Editor-in-Chief:'Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Jinhui Wu, MD
Please Join in Editing This Page and Apply to be an Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Overview of astrocytoma?
Astrocytoma is a type of glioma that origins from astrocytes. Astrocytes can support and nourish neurons and help repair the damage when the brain is injured. Astrocytoma occupies 30% of brain tumors. Usual symptoms include headache, nausea and vomiting, seizure, hydrocephalus, weakness, or numbness in the extremities. Sometimes astrocytoma may spread along the cerebrospinal fluid pathways, but rare spread outside of the brain or spinal cord. Head magnetic resonance imaging (MRI) is the best way for diagnosis. Treatments include surgery, radiation therapy, chemotherapy, gene therapy, or a combination of them. Becayse most astrocytomas can spread widely throughout the normal brain tissue, it may be very hard to remove by surgery. Prognosis depends on the grade of the cancer.
See also
Where to find medical care for astrocytoma?
Directions to Hospitals Treating astrocytoma