Intracranial Ewing sarcoma with obstructive hydrocephalus in pediatric patient: a rare case report
-
Published:2023-12-10
Issue:3
Volume:12
Page:3404-3406
-
ISSN:2302-2914
-
Container-title:Bali Medical Journal
-
language:
-
Short-container-title:Bali Med J.
Author:
Prasetya Galan Budi,Parenrengi Muhammad Arifin,Suryaningtyas Wihasto
Abstract
Link of Video Abstract: https://youtu.be/b4jB7Jos8tw
Background: Ewing’s sarcoma is the second most common primary bone tumor presenting in childhood and adolescence. Ewing's sarcoma of the skull bones is an unusual occurrence (6 to 9% of all Ewing’s. sarcoma cases). Here, we present a rare case of Ewing's sarcoma involving the central nervous system (CNS) in a 13-month-old child and share our experience with its management.
Case Presentation: We report a case of a 13-month-old girl with a chief complaint of gradually progressive head size. There is a history of seizures once a week before admission. The head CT scan with contrast administration revealed non-communicating hydrocephalus with bone defect in the occipital region and an intraaxial tumor of the posterior fossa due to Ewing’s sarcoma.
Conclusion: Primary cranial Ewing's sarcoma of the cranium is a rare occurrence; its extension to intraparenchymal is even rare. This diagnosis can be considered in the differential diagnosis in children with a tumor involving the skull with destruction of the bone.
Publisher
DiscoverSys, Inc.