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原发性枕部尤因肉瘤伴随后期脊柱播散。

Primary Occipital Ewing's Sarcoma with Subsequent Spinal Seeding.

作者信息

Alqahtani Ali, Amer Roaa, Bakhsh Eman

机构信息

College of Medicine, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.

Radiology Department, King Fahad Medical City, Riyadh, Saudi Arabia.

出版信息

Case Rep Pediatr. 2017;2017:1521407. doi: 10.1155/2017/1521407. Epub 2017 Jun 13.

Abstract

Ewing's sarcoma is a primary bone cancer that mainly affects the long bones. This malignancy is particularly common in pediatric patients. Primary cranial involvement accounts for 1% of cases, with occipital involvement considered extremely rare. In this case study, primary occipital Ewing's sarcoma with a posterior fossa mass and subsequent relapse resulting in spinal seeding is reported. A 3-year-old patient presented with a 1-year history of left-sided headaches, localized over the occipital bone with progressive torticollis. Computed tomography (CT) imaging showed a mass in the left posterior fossa compressing the brainstem. The patient then underwent surgical excision followed by adjuvant chemoradiation therapy. Two years later, the patient presented with severe lower back pain and urinary incontinence. Whole-spine magnetic resonance imaging (MRI) showed cerebrospinal fluid (CSF) seeding from the L5 to the S4 vertebrae. Primary cranial Ewing's sarcoma is considered in the differential diagnosis of children with extra-axial posterior fossa mass associated with destructive permeative bone lesions. Although primary cranial Ewing's sarcoma typically has good prognosis, our patient developed metastasis in the lower spine. Therefore, with CNS Ewing's sarcoma, screening of the entire neural axis should be taken into consideration for early detection of CSF seeding metastasis in order to decrease the associated morbidity and mortality.

摘要

尤因肉瘤是一种主要影响长骨的原发性骨癌。这种恶性肿瘤在儿科患者中尤为常见。原发性颅骨受累占病例的1%,枕骨受累极为罕见。在本病例研究中,报告了一例原发性枕部尤因肉瘤伴后颅窝肿块,随后复发导致脊髓播散。一名3岁患者有1年左侧头痛病史,疼痛局限于枕骨,伴有进行性斜颈。计算机断层扫描(CT)成像显示左后颅窝有一肿块压迫脑干。该患者随后接受了手术切除,随后进行辅助放化疗。两年后,患者出现严重下背痛和尿失禁。全脊柱磁共振成像(MRI)显示脑脊液(CSF)从L5至S4椎体播散。在鉴别诊断伴有破坏性浸润性骨病变的轴外后颅窝肿块儿童时,应考虑原发性颅骨尤因肉瘤。虽然原发性颅骨尤因肉瘤通常预后良好,但我们的患者发生了下脊柱转移。因此,对于中枢神经系统尤因肉瘤,应考虑对整个神经轴进行筛查,以便早期发现脑脊液播散转移,从而降低相关的发病率和死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3126/5485299/0a1ff625f578/CRIPE2017-1521407.001.jpg

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