Paediatric Ependymoma- A Rare Case Report
DOI:
https://doi.org/10.46858/vimshsj.110407Keywords:
Paediatric ependymoma, Sellar tumour, Intracranial tumours, Hydrocephalus managementAbstract
Ependymomas are rare central nervous system (CNS) tumours originating from ependymal cells lining the ventricles and spinal cord. This case report details a unique presentation of a sellar ependymoma in a 2-year-old male presenting with acute symptoms, including inability to walk and vomiting. Magnetic resonance imaging (MRI) revealed a large sellar and suprasellar mass causing hydrocephalus. The patient underwent a parieto-occipital craniotomy with complete tumour excision and placement of a ventriculoperitoneal shunt to manage hydrocephalus.
Downloads
References
Lavrador J, Oliveira E, Teixeira J, et al. Adult supratentorial extraventricular anaplastic ependymoma: therapeutic approach and clinical review. Asian J Neurosurg 2018;13:105–109.
Wang M, Zhang R, Liu X, et al. Supratentorial cortical ependymomas: a retrospective series of 13 cases at a single center. World Neurosurg 2018;112:e772–e777.
Leng X, Tan X, Zhang C, et al. Magnetic resonance imaging findings of extraventricular anaplastic ependymoma: a report of 11 cases. Oncol Lett 2016;12:2048–54.
Newton HB, Henson J, Walker RW. Extraneural metastases in ependymoma. J Neurooncol. 1992; 14: 135-142. PubMed
Nazar GB, Hoffman HJ, Becker LE, Jenkin D, Humphreys RP, Hendrick EB: Infratentorial ependymomas in childhood: Prognostic factors and treatment. J Neurosurg 1990;72:408–417.
Cohen ME, Duffner PK: Brain Tumors in Children. Principles of Diagnosis and Treatment. New York, Raven Press, 1994.
Published
How to Cite
Issue
Section
Copyright (c) 2025 Dr. Rishab Singh Deo, Dr. V. G. Deshpande , Dr. G. B. Machale, Dr. Suresh Waydande, Dr. Sunil Natha Mhaske
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.