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CASE REPORT
Year : 2017  |  Volume : 12  |  Issue : 1  |  Page : 139-141

Choroid plexus papilloma


Department of Pathology, VMMC and Safdarjang Hospital, New Delhi, India

Correspondence Address:
Divya Sethi
Senior Resident, Department of Pathology, VMMC and Safdarjang Hospital, New Delhi
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1793-5482.153501

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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.


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