Choroid Plexus Carcinoma (WHO Grade III): A Rare Case of Central Nervous System Tumour in Two Years Old Girl

Authors

  • Sunderesh Kamal Chander
  • B Vinothkumar
  • P M Yamini
  • Sonti Sulochana

Keywords:

Choroid Plexus Carcinoma, Central Nervous System Tumours, Choroid Plexus Papilloma, Atypical Choroid Plexus

Abstract

Choroid plexus tumours represent 0.3 to 0.6% of all central nervous system tumors. The pediatric age group has a higher prevalence of malignancies originating from the choroid plexus epithelium. We reported a case of 2yr old female child who presented with projectile vomiting for the past 2 weeks to Neurosurgery. On CT scan brain showed a large heterogeneous density mass with perilesional oedema. Craniotomy and debulking of the tumors through a transylvian fissure were done. Intraoperatively, the tumor was fragile, soft, and highly vascular. On HPE, tumor was Grade III choroid plexus.

Downloads

Download data is not yet available.

Downloads

Published

10-10-2023

How to Cite

1.
Chander SK, Vinothkumar B, Yamini PM, Sulochana S. Choroid Plexus Carcinoma (WHO Grade III): A Rare Case of Central Nervous System Tumour in Two Years Old Girl. JK Science [Internet]. 2023 Oct. 10 [cited 2024 Dec. 22];25(4):258-60. Available from: https://journal.jkscience.org/index.php/JK-Science/article/view/231

Issue

Section

CASE REPORTS

Similar Articles

1 2 3 4 5 6 > >> 

You may also start an advanced similarity search for this article.