AB007. Intramedullary schwannoma: a rare case report
Abstract

AB007. Intramedullary schwannoma: a rare case report

Vidia Meiranda Akib1, Yunni Diansari2

1Department of Neurology, Sriwijaya University, Palembang, Indonesia; 2Department of Neurology, Dr. Moh Hoesin Hospital Palembang, Palembang, Indonesia

Correspondence to: Vidia Meiranda Akib, MD. Neurology Resident, Department of Neurology, Sriwijaya University, Palembang, South Sumatera, Indonesia. Email: vidiafkub2010@gmail.com.

Background: Intramedullary schwannomas are a rare case, accounting for only 0.3% of all intraspinal neoplasms and 1.1% of spinal schwannomas. These tumors have most often been reported to involve a single lesion affecting the cervical spinal cord (63%), the thoracic spinal cord (26%), and the lumbar spinal cord (11%). Here we report a very rare case thoracic intramedullary schwannoma.

Case Description: A 24-year-old female patient was admitted with gradual onset weakness of both lower limbs for last 2 years with retention of urine. Neurological examination revealed the motor strengths on both legs were 2. There was a sensibility dissociation below Th8 dermatomal level. Magnetic resonance imaging shows an ill-demarcated intramedullary lesion extending from Th8 to Th9 accompanied by spinal cord edema along Th4 to Th11. The surgery was performed with standard posterior middle approach. Laminectomy decompression was performed and dura opened in the midline. Infiltrative nature of the mass made the total resection impossible. Histopathological result followed by immunohistochemistry confirmed the diagnosis of schwannoma. In the postoperative follow-up, the motor strengths of both legs are absent and no clinical improvement at all until now. Prior to surgery, intramedullary schwannoma is often misdiagnosed as other types of tumour, including ependymoma, astrocytoma and hemangioblastoma, due to its atypical imaging appearance and low incidence. Surgery for spinal intramedullary tumors remains one of the major challenges for surgeons, due to their relative infrequency, and surgical difficulty technique. Worse preoperative McCormick Scale, thoracic tumor location, partial resection, and lack of availability of intraoperative neurophysiology monitoring (IONM) were significant factors for poor prognosis.

Conclusions: Intramedullary schwannomas are slow-growing rare tumors and should be considered as one of the differential diagnoses for the intramedullary spinal lesions. Magnetic resonance imaging may be helpful for diagnosis however clear distinction cannot be made between the intramedullary spinal lesions. Total surgical resection is the treatment choice for this patient but infiltrative lesions cannot be resected completely for which radiotherapy has been suggested.

Keywords: Intramedullary schwannomas; McCormick Scale; laminectomy; case report


Acknowledgments

Funding: None.


Footnote

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at https://cco.amegroups.com/article/view/10.21037/cco-24-ab007/coif). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee(s) and with the Helsinki Declaration (as revised in 2013). Written informed consent was obtained from the patient for the publication of this case report and accompanying images. A copy of the written consent is available for review by the editorial office of this journal.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the noncommercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


Cite this abstract as: Akib VM, Diansari Y. AB007. Intramedullary schwannoma: a rare case report. Chin Clin Oncol 2024;13(Suppl 1):AB007. doi: 10.21037/cco-24-ab007

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