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Intramedullary primary spinal cord melanoma: illustrative case
Akash Mishra1, Danielle Golub2, Daniel Schneider2
1Zucker School of Medicine at Hofstra University/Northwell Health, Hempstead, New York.
Journal of Neurosurgery. Case Lessons
|March 10, 2025
Summary
Intramedullary primary spinal melanoma (IPSM) is a rare spinal tumor. Diagnosis requires surgical pathology, and optimal treatment may involve resection, radiation, and systemic therapies.
Area of Science:
- Neuro-oncology
- Spinal Surgery
- Oncology
Background:
- Intramedullary primary spinal melanoma (IPSM) is an exceptionally rare spinal tumor.
- Limited data exists on its clinical, radiographic, histopathological, and genetic characteristics, as well as management strategies.
Purpose of the Study:
- To describe a case of intramedullary primary spinal melanoma (IPSM).
- To highlight the diagnostic challenges and potential treatment pathways for this rare condition.
Main Methods:
- A 49-year-old male with progressive upper-extremity radiculopathy underwent MRI, revealing an intramedullary C6-T1 tumor.
- Surgical resection was performed using intraoperative dorsal column mapping for safe myelotomies.
- Histopathological analysis confirmed melanoma, with further workup excluding other primary sites.
Main Results:
- Gross-total resection of the intramedullary tumor was achieved.
- Postoperatively, the patient experienced mild sensory deficits but maintained full motor strength.
- Diagnosis of IPSM was confirmed, and the patient was planned for adjuvant radiation and immunotherapy.
Conclusions:
- Fewer than 40 cases of IPSM have been reported globally.
- Diagnosis relies on surgical pathology, often preceded by progressive symptoms and characteristic imaging.
- Multimodal treatment including surgery, radiation, and systemic therapies is likely optimal, with potential for molecular markers to guide future treatment.

