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腰椎神经根原发性骨外尤文肉瘤:一例报告。

Primary extraskeletal Ewing's sarcoma of the lumbar nerve root: A case report.

作者信息

Lei Li-Hui, Li Feng, Wu Tao

机构信息

Department of Spinal Surgery, Huaihua First People's Hospital, Huaihua 418000, Hunan Province, China.

Department of Technology, Hunan University of Medicine, Huaihua 418000, Hunan Province, China.

出版信息

World J Clin Cases. 2022 May 26;10(15):4942-4948. doi: 10.12998/wjcc.v10.i15.4942.

DOI:10.12998/wjcc.v10.i15.4942
PMID:35801040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9198884/
Abstract

BACKGROUND

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.

CASE SUMMARY

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.

CONCLUSION

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.

摘要

背景

尤因肉瘤(ES)是一种侵袭性很强的骨恶性肿瘤。起源于椎管的骨外尤因肉瘤(EES)极为罕见。在此,我们报告一例罕见的原发性腰段脊神经根EES病例,包括完整的诊断和治疗过程。

病例摘要

一名年轻女性患者因右下肢疼痛1个月就诊。磁共振成像(MRI)显示腰段硬膜外区域有一个11mm×14mm×31mm的肿块,在第五腰椎(L5)水平向右侧L5神经孔延伸。我们最初的诊断是硬膜外神经鞘瘤。患者接受了全椎板切除术、肿瘤切除术和椎弓根螺钉内固定术,术中发现L5神经根肿瘤已被完全切除。病变的组织病理学检查显示为典型的ES,有大量小圆形细胞。免疫组织化学分析显示CD99和S100呈阳性。术后,患者接受了化疗和放疗,随访1年,脊柱MRI和正电子发射断层扫描/计算机断层扫描复查未发现复发性肿瘤或新病变。

结论

临床上,当在椎管内外遇到神经根肿瘤时,应考虑骨外ES,诊断应通过病理活检确定。手术切除后,应进行化疗和放疗。治疗后,应积极随访并定期复查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/914c/9198884/07dfd041a1d9/WJCC-10-4942-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/914c/9198884/13f74eae10df/WJCC-10-4942-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/914c/9198884/477a621ceebd/WJCC-10-4942-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/914c/9198884/07dfd041a1d9/WJCC-10-4942-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/914c/9198884/13f74eae10df/WJCC-10-4942-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/914c/9198884/477a621ceebd/WJCC-10-4942-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/914c/9198884/07dfd041a1d9/WJCC-10-4942-g003.jpg

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