Case Report Volume 15 Issue 9 - 2026

Pilocytic Astrocytoma of the Brainstem in a Child Followed for Hereditary Spherocytosis: A Case Report

Sarah Lembarki*, Fatma Ez Zahrae El Malki, Nazik Allali, Latifa Chat and Siham EL Haddad

Department of Radiology, Pediatric Hospital, CHU Ibn Sina, Faculty of Medicine and Pharmacy of Rabat, Rabat, Morocco

*Corresponding Author: Sarah Lembarki, Department of Radiology, Pediatric Hospital, CHU Ibn Sina, Faculty of Medicine and Pharmacy of Rabat, Rabat, Morocco.
Received: August 10, 2026; Published: August 25, 2026



The majority of pediatric brain tumors originate within the posterior fossa, most commonly including juvenile pilocytic astrocytomas, medulloblastomas (MB), ependymomas, and brainstem gliomas. This report describes the case of a 10-year-old patient with underlying hereditary microspherocytosis presenting with headaches, vomiting, and a cerebellar syndrome. Brain computed tomography (CT) and brain magnetic resonance imaging (MRI) with magnetic resonance spectroscopy (MRS), displaying classic features, revealed a well-circumscribed dual cystic-solid lesion of the medulla oblongata without obstructive hydrocephalus. Pilocytic astrocytoma, ganglioglioma, ependymoma, and hemangioblastoma are among the main differential diagnoses.

Keywords: Pilocytic Astrocytoma; Brainstem; Cerebellar Syndrome; MRI; Magnetic Resonance Spectroscopy; Child

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Sarah Lembarki., et al. “Pilocytic Astrocytoma of the Brainstem in a Child Followed for Hereditary Spherocytosis: A Case Report”. EC Paediatrics 15.9 (2026): 01-05.