Choroid plexus papilloma
Choroid Plexus Papilloma
Choroid Plexus Papilloma (pronunciation: /ˈkɔːrɔɪd ˈplɛksəs pəˈpɪləmə/) is a rare type of brain tumor that originates in the choroid plexus of the brain.
Etymology
The term 'Choroid Plexus Papilloma' is derived from the Greek words 'chorion' meaning skin, 'plexis' meaning braid, and 'papilloma' meaning small wart.
Definition
A Choroid Plexus Papilloma is a benign, slow-growing tumor that arises from the cells of the choroid plexus. These tumors are most commonly found in children, but can occur at any age.
Symptoms
Symptoms of Choroid Plexus Papilloma can vary depending on the location and size of the tumor. Common symptoms include headache, nausea, vomiting, and problems with balance or coordination.
Diagnosis
Diagnosis of Choroid Plexus Papilloma typically involves a combination of neurological examination, imaging studies such as MRI or CT scan, and sometimes biopsy of the tumor.
Treatment
Treatment for Choroid Plexus Papilloma usually involves surgical removal of the tumor. In some cases, radiation therapy or chemotherapy may be used as well.
Prognosis
The prognosis for Choroid Plexus Papilloma is generally good, especially if the tumor can be completely removed. However, long-term follow-up is necessary due to the risk of recurrence.
Related Terms
- Choroid plexus carcinoma
- Brain tumor
- Neurological examination
- MRI
- CT scan
- Biopsy
- Radiation therapy
- Chemotherapy
External links
- Medical encyclopedia article on Choroid plexus papilloma
- Wikipedia's article - Choroid plexus papilloma
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