Choroid plexus tumor

From WikiMD.org
Jump to navigation Jump to search

Choroid Plexus Tumor

Choroid Plexus Tumor (pronunciation: koh-royd plek-sus too-mer) is a rare type of brain tumor that originates in the choroid plexus, a network of cells that produce the cerebrospinal fluid (CSF) in the ventricles of the brain.

Etymology

The term "Choroid Plexus Tumor" is derived from the Greek words "chorion" meaning skin or membrane, and "plexus" meaning braid or network, referring to the network of cells in the brain where these tumors originate.

Types

There are three types of Choroid Plexus Tumors:

Symptoms

Symptoms of a Choroid Plexus Tumor can vary depending on the size and location of the tumor, but may include:

Diagnosis

Diagnosis of a Choroid Plexus Tumor typically involves a neurological examination, imaging tests such as MRI or CT scan, and a biopsy to examine the cells of the tumor.

Treatment

Treatment for a Choroid Plexus Tumor may include surgery to remove the tumor, radiation therapy, and/or chemotherapy.

Prognosis

The prognosis for a Choroid Plexus Tumor depends on a variety of factors, including the type of tumor, its size and location, and the patient's overall health.

See Also

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski