J Korean Neurosurg Soc.  1988 Aug;17(4):717-728.

Primary Third Ventricular Tumors

Affiliations
  • 1Department of Neurosurgery, College of Medicine, Seoul National University, Korea.

Abstract

Intrathird ventricular tumors that mainly occupy the ventricle cavity without extending to the neighbouring structures are rare. These tumors are developed from the choroids plexus, tela, ependyma, subjacent neuroglia and embryonic cell rest. The authors experienced 11 cases of rare intrathird ventricular tumors during the past 10 years. During the same period, number of surgically proven brain tumors were 990 and intrathird ventricular tumors comprised 1.1%. These are two cases of choroids plexus papillomas, three craniopharyngiomas, two germ cell tumors, one meningioma, one glioependymal cyst, one ependymoma, one astrocytoma. Suprasellar craniopharyngiomas, thalamic gliomas, optic and hypothalamic gliomas were excluded. The age distribution was from 6 years old to 59 years old. The clinical manifestation was characteristic in that they usually had the sudden intermittent headache without specific localizing signs. Surgical approach to this area is by transcallosal or transcortical approach. Surgical total removal was quite feasible by either approach and outcome was rather favorable.

Keyword

Third ventricle tumor; Choroid plexus papilloma; Craniopharyngioma; Meningioma; Germ cell tumor

MeSH Terms

Age Distribution
Astrocytoma
Brain Neoplasms
Child
Choroid
Craniopharyngioma
Ependyma
Ependymoma
Glioma
Headache
Humans
Meningioma
Middle Aged
Neoplasms, Germ Cell and Embryonal
Neuroglia
Optic Nerve Glioma
Papilloma
Papilloma, Choroid Plexus
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