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