Solomou Aikaterini, Panagiotopoulos Vasileios, Kraniotis Pantelis, Apostolopoulou Katerina, Tzortzidis Fotis
Department of Radiology, University Hospital of Patras, Patras, Greece.
Department of Neurosurgery, University Hospital of Patras, Patras, Greece.
BJR Case Rep. 2017 Jun 14;3(4):20170009. doi: 10.1259/bjrcr.20170009. eCollection 2017.
Spinal cord intramedullary lipomas are rare, comprising 2% of intramedullary tumours. They are more often associated with spinal dysraphism, while lipomas not associated with spinal dysraphism are even less frequent, accounting for 1% of cases. The pathogenesis of spinal cord intramedullary lipomas remains unclear. MRI is the gold standard for the evaluation of these lesions. We hereby present a case of a 37-year-old male, who underwent MRI due to spastic paraparesis. MRI revealed a bilocular, spinal cord intramedullary lesion at the level of - , with dilatation of the spinal canal and signal characteristics compatible with lipoma. There was no clear imaging evidence of spinal dysraphism. The patient underwent surgery and diagnosis was confirmed histopathologically.
脊髓髓内脂肪瘤较为罕见,占髓内肿瘤的2%。它们更常与脊髓发育异常相关,而与脊髓发育异常无关的脂肪瘤则更为少见,占病例的1%。脊髓髓内脂肪瘤的发病机制尚不清楚。MRI是评估这些病变的金标准。我们在此报告一例37岁男性患者,因痉挛性截瘫接受了MRI检查。MRI显示在 - 水平有一个双房性脊髓髓内病变,伴有椎管扩张,信号特征符合脂肪瘤。没有明确的影像学证据表明存在脊髓发育异常。患者接受了手术,组织病理学确诊。