Imaging Features of Intramedullary Spinal Cord Lesions with Histopathological Correlation

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Purpose Most of the intramedullary spinal cord lesions have a component of insidious myelopathic changes at the time of diagnosis. Among the spinal cord lesions, intramedullary neoplasms are rare (25%). They represent 4 to 10% of all central nervous system tumors. But due to involvement of tracts, they are associated with significant neurological symptoms. Their imaging features can help early diagnosis and predict prognosis. We aim to narrow down differential diagnoses of intramedullary lesions based on imaging findings.

Materials and Methods This retrospective study included 40 patients as a sample that underwent magnetic resonance imaging spine at our institution (on 3T machine). Patient population had varied clinical complaints, ranging from headache, nausea, vomiting, motor weakness, bladder and bowel involvement, progressive paraparesis to paraplegia. Lesions were evaluated site, size, margin, associated cysts, signal intensity, enhancement, and associated syringohydromyelia.

Results This study obtained majority of the lesions to be ependymoma (15) and astrocytoma (11), followed by infection (4), hemangioblastoma (3), and metastasis (2). Five patients were either lost to follow-up or not operated on.

Conclusion Most of the intramedullary lesions were malignant and were showing postcontrast enhancement. Ependymomas were more frequently present in cervical region, central in location with well-defined margins and focal postcontrast enhancement. Among the total of 15 ependymomas, three cases were associated with neurofibromatosis-2. Ependymomas were more frequently associated with syringohydromyelia and peripheral hemorrhage (cap sign). Astrocytoma was more frequently seen in children, thoracic and eccentric in location with ill-defined margins. Enhancement in astrocytoma was dependent on the grade of tumor. Metastasis was a differential, with imaging characteristics dependent on type of primary. Intramedullary granuloma due to infection can also be confusing mimics of neoplasm. High-velocity signal loss due to flow voids is seen in the hemangioblastomas.

Keywords spinal cord lesions - MRI - spinal cord lesions - ependymoma - astrocytoma - metastasis - granuloma Ethics Approval and Consent to Participate

Granted; OBSERVATIONAL STUDY. The patients' information was kept confidential.


Consent for Publication

The written informed consent was obtained from all research participants after a full explanation of the study.


Availability of Data and Materials

The datasets during and/or analyzed during the current study are available from the corresponding author on a reasonable request.


Authors' Contributions

BS was involved in conceptualization, design, the definition of intellectual content, literature search, clinical studies, experimental studies, data acquisition, data analysis, statistical analysis, manuscript preparation, and manuscript editing. GR contributed to designing, definition of intellectual content and literature search. AC was involved in definition of intellectual content, statistical analysis, manuscript editing, and manuscript review. All the authors contributed to study design, data collection, drafting of the manuscript, revision and reading of the manuscript and approved its final version.


Ethical Approval

This study was approved by Institutional Ethics Committee. All MRI examinations performed in the studies involving human participants were in accordance with the ethical standards of the Institutional Ethics Committee.

Publication History

Article published online:
14 July 2022

© 2022. Spring Hope Cancer Foundation & Young Oncologist Group of Asia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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