Choroid plexus tumors

Authors

  • Yuriy Orlov Romodanov Neurosurgery Institute, Kiev, Ukraine
  • Andrii Shaverskyi Romodanov Neurosurgery Institute, Kiev, Ukraine https://orcid.org/0000-0002-3776-5563
  • Аndriy Svyst Romodanov Neurosurgery Institute, Kiev, Ukraine

DOI:

https://doi.org/10.25305/unj.59041

Keywords:

choroid plexus tumor, hydrocephalus, cerebrospinal fluid-shunting operations, children, adults

Abstract

Introduction. In the article the data of literature are summarized and age-related features of choroid plexus tumors clinical flow, diagnostics, localization and outcomes in children and adults are considered.

Materials and methods. The research is based on retrospective analysis of case reports of patients been treated in Institute for period of 30 years.

Results. Choroid plexus tumors — are rare primary neoplasms from neuroepithelial tissue. They make from 0.4 to 1% in structure of all intracranial tumors. Most often they are found in infants.

Conclusions. Treatment of these patients is complicated by chorioid plexus tumors’ high vascularity, accompanying hydrocephalus and ineffective adjuvant therapy of choroid plexus carcinomas.

Author Biographies

Yuriy Orlov, Romodanov Neurosurgery Institute, Kiev

Pediatric Neurosurgery Department

Andrii Shaverskyi, Romodanov Neurosurgery Institute, Kiev

Pediatric Neurosurgery Department

Аndriy Svyst, Romodanov Neurosurgery Institute, Kiev

Pediatric Neurosurgery Department

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Published

2012-06-26

How to Cite

Orlov, Y., Shaverskyi, A., & Svyst А. (2012). Choroid plexus tumors. Ukrainian Neurosurgical Journal, (2), 13–17. https://doi.org/10.25305/unj.59041

Issue

Section

Original articles