Li Wai-Yung, Brock Penelope, Saunders Dawn E
Departments of Radiology, Great Ormond Street Hospital for Children, Great Ormond Street, London, WC1N 3JH, UK.
Pediatr Radiol. 2005 Jun;35(6):612-8. doi: 10.1007/s00247-005-1438-2. Epub 2005 Apr 7.
Ewing sarcoma accounts for 10-15% of all childhood malignant bone tumours and is second in prevalence to osteosarcoma. The skull bones are an unusual site of origin of primary Ewing sarcoma in children. Previous reports concentrate on the neurosurgical aspects and relatively good outcome compared to other bone tumours of the calvarium. Reported cases mainly describe the imaging characteristics on CT.
To describe the MRI and CT features of primary cranial Ewing sarcoma.
The neuroimaging of three cases of primary cranial Ewing sarcoma are reviewed.
Our three cases show an extra-axial mass that is high attenuation on CT and low signal on T2-weighted MRI. Haemorrhagic components, dural extension and contrast enhancement are also characteristic features.
CT attenuation and magnetic resonance signal characteristics reflect sheets of densely packed cells seen in Ewing sarcoma.
尤因肉瘤占所有儿童恶性骨肿瘤的10% - 15%,在发病率上仅次于骨肉瘤。颅骨是儿童原发性尤因肉瘤不常见的起源部位。既往报道主要集中在神经外科方面以及与颅骨其他骨肿瘤相比相对较好的预后。报道的病例主要描述了CT上的影像学特征。
描述原发性颅骨尤因肉瘤的MRI和CT特征。
回顾了3例原发性颅骨尤因肉瘤的神经影像学表现。
我们的3例病例显示为轴外肿块,在CT上呈高密度,在T2加权MRI上呈低信号。出血成分、硬膜受累及强化也是其特征性表现。
CT密度和磁共振信号特征反映了尤因肉瘤中密集排列的细胞片。