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CC BY-NC-ND 4.0 · Asian J Neurosurg 2017; 12(01): 139-141
DOI: 10.4103/1793-5482.153501
CASE REPORT

Choroid plexus papilloma

Divya Sethi
Department of Pathology, VMMC and Safdarjang Hospital, New Delhi
,
Rashmi Arora
Department of Pathology, VMMC and Safdarjang Hospital, New Delhi
,
Ketan Garg
Department of Pathology, VMMC and Safdarjang Hospital, New Delhi
,
Parul Tanwar
Department of Pathology, VMMC and Safdarjang Hospital, New Delhi
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Choroid plexus tumors are rare intracranial tumors which account for only 0.4-0.6% of all brain tumors. These are intraventricular papillary neoplasms derived from choroid plexus epithelium and range from choroid plexus papillomas (World Health Organisation (WHO) grade I) to choroid plexus carcinomas (WHO grade III). It is an important albeit rare cause of hydrocephalous. We present to you the case of a 1-year-old child who presented with the signs and symptoms of hydrocephalous and was diagnosed as choroid plexus papilloma on histopathology.

Key-words:

Choroid plexus - lateral ventricle - papilloma


Publikationsverlauf

Artikel online veröffentlicht:
20. September 2022

© 2017. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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