Shihadeh Omar M, Khan Muhammad Mohsin, Salih Hayel, Thabet Abdelnaser, Belkhair Sirajeddin
Neurosurgery, Hamad Medical Corporation, Doha, QAT.
Neurosurgery, Weill Cornell Medicine-Qatar, Doha, QAT.
Cureus. 2023 Jul 30;15(7):e42687. doi: 10.7759/cureus.42687. eCollection 2023 Jul.
Ewing sarcoma is a rare neoplasm that mostly grows in bones or soft tissues around bones. Most cases of Ewing sarcoma occur in intra-skeletal locations (long bones, pelvis, or ribs) and rarely in extra-skeletal regions such as paravertebral or epidural space, whereas a primary intradural extramedullary Ewing sarcoma (IEES) is extremely rare. Fifty cases of primary IEES including our case were identified in the literature, so far, of which two-thirds are in the lumbosacral region, while only 12 reports described a cervical location of the tumor. Herein, we are presenting a case of C7-T1 primary IEES for a 24-year-old male, followed by a review of updated literature about the primary IEES in the cervical spine.
尤因肉瘤是一种罕见的肿瘤,主要生长于骨骼或骨骼周围的软组织。大多数尤因肉瘤病例发生于骨骼内部(长骨、骨盆或肋骨),很少发生于椎旁或硬膜外间隙等骨骼外区域,而原发性硬脊膜内髓外尤因肉瘤(IEES)极为罕见。迄今为止,文献中已报道了包括我们的病例在内的50例原发性IEES病例,其中三分之二位于腰骶部,而仅有12篇报道描述了肿瘤位于颈椎。在此,我们报告一例24岁男性C7-T1原发性IEES病例,并对颈椎原发性IEES的最新文献进行综述。