Published online May 26, 2022. doi: 10.12998/wjcc.v10.i15.4942
Peer-review started: September 30, 2021
First decision: January 11, 2022
Revised: January 20, 2022
Accepted: April 3, 2022
Article in press: April 3, 2022
Published online: May 26, 2022
Processing time: 236 Days and 0.7 Hours
Ewing’s sarcoma (ES) is a highly aggressive bone malignancy. Extraskeletal ES (EES) originating in the spinal canal is extremely rare. Herein, we report on a rare case of EES with a primary lumbar spinal nerve root including the complete diagnosis and treatment.
A young female patient presented with a complaint of right lower limb pain for 1 mo. Magnetic resonance imaging (MRI) revealed an 11 mm × 14 mm × 31 mm mass in the lumbar epidural region extending at the fifth lumbar spine (L5) level toward the right L5 neural foramen. Our initial diagnosis was an epidural schwannoma. The patient underwent total laminectomy, tumor resection and pedicle screw internal fixation and the L5 root tumor was found to have been completely removed intraoperatively. Histopathological examination of the lesion showed a typical ES with a large number of small, round cells. Immunohistochemistry analysis indicated positive CD99 and S100. After surgery, the patient received chemotherapy and radiotherapy with a 1 year of follow-up and no recurrent tumors or new lesions were found upon spine MRI and positron emission tomography/computed tomography reexamination.
Clinically, ES outside the bone should be considered when nerve root tumors are encountered inside and outside the spinal canal and the diagnosis should be determined by pathological biopsy. After surgical resection, chemotherapy and radiotherapy should be performed. After treatment, active follow-up and regular review should be completed.
Core Tip: Ewing’s sarcoma (ES) is a very aggressive primary bone malignancy. Extraskeletal ES (EES) itself is rare, and primary intraspinal EES is even rarer, accounting for only 5% of all ES cases. Within the spine, these malignancies are typically located in the paravertebral and epidural spaces. Both domestically and internationally, most reported cases of EES have been found in the spinal canal. Primary nerve root EES is rare with only a few cases reported. Involvement of the lumbar nerve roots in EES has not been previously reported. Herein, we report a case of EES with primary intramedullary lumbar 5 nerve root including complete diagnosis and treatment.