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蝶骨原发性尤因肉瘤伴不寻常影像学表现:一例报告

Primary Ewing's sarcoma of the sphenoid bone with unusual imaging features: a case report.

作者信息

Sharma Ashwani, Garg Ajay, Mishra Nalini K, Gaikwad Shailesh B, Sharma Mehar C, Gupta Vipul, Suri Ashish

机构信息

Department of NeuroRadiology, Neurosciences Center, All India Institute of Medical Sciences, Ansari Nagar, New Delhi 110029, India.

出版信息

Clin Neurol Neurosurg. 2005 Oct;107(6):528-31. doi: 10.1016/j.clineuro.2004.11.001. Epub 2004 Dec 13.

Abstract

Ewing's sarcomas (ES) account for approximately 10% of primary malignant bone tumors. Primary Ewing's sarcoma of the skull is a very rare entity. We report a case of Ewing's sarcoma of the sphenoid bone in a 5-year-old boy. CT scan showed heterogeneously enhancing mass with associated spiculated new bone formation along the posterolateral wall of the orbit. Magnetic resonance (MR) imaging showed markedly heterogeneously signal intensity mass lesion containing areas of hemorrhage and fluid-fluid levels. Spiculated new bone formation and fluid-fluid levels had not been reported previously in skull Ewing's sarcomas and may be helpful features for preoperative diagnosis.

摘要

尤因肉瘤(ES)约占原发性恶性骨肿瘤的10%。颅骨原发性尤因肉瘤是一种非常罕见的疾病。我们报告一例5岁男孩蝶骨尤因肉瘤病例。CT扫描显示不均匀强化肿块,沿眼眶后外侧壁有相关的毛刺状新骨形成。磁共振(MR)成像显示明显不均匀信号强度的肿块病变,含有出血区和液-液平面。毛刺状新骨形成和液-液平面此前在颅骨尤因肉瘤中尚未见报道,可能是术前诊断的有用特征。

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