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A rare case of Ewing's sarcoma primary of the cervical spine in a 1-year-old child: A case report and literature review.

Authors :
Shaker K
Alomar K
Wahoob M
Altabaa K
Omran M
Marwa G
Source :
International journal of surgery case reports [Int J Surg Case Rep] 2024 Sep; Vol. 122, pp. 110020. Date of Electronic Publication: 2024 Jul 14.
Publication Year :
2024

Abstract

Introduction and Significance: Ewing sarcoma is a rare and malignant bone tumor that can primarily affect the cervical spine. Symptoms may not always be present, but muscle weakness is a critical indicator of disease progression and necessitates urgent surgical intervention to relieve pressure on the spinal cord.<br />Case Presentation: We present a case of a child who experienced sudden muscle weakness in the left upper limb. An MRI of the spine revealed a tumor in the cervical spine compressing the spinal cord. Urgent surgical intervention was performed, successfully removing most of the tumor. This was followed by complementary chemotherapy.<br />Clinical Discussion: Tumors located in the cervical spine are challenging to treat due to their location. Urgent surgery may be crucial when muscle weakness is present. This case demonstrates a novel surgical approach through the spinous processes of the vertebrae, avoiding laminectomy and the need for spinal fixation, which can be difficult in children.<br />Conclusion: Our case highlights a rare presentation of Ewing sarcoma in the cervical spine, infrequently reported in medical literature. It also demonstrates the success of a novel surgical approach that avoids spinal fixation in children.<br />Competing Interests: Conflict of interest statement The authors declare that they have no competing interests.<br /> (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Details

Language :
English
ISSN :
2210-2612
Volume :
122
Database :
MEDLINE
Journal :
International journal of surgery case reports
Publication Type :
Academic Journal
Accession number :
39043091
Full Text :
https://doi.org/10.1016/j.ijscr.2024.110020