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Clinical Image of a Spinal Ependymoma Discovered 8 Years after Initial Misdiagnosis as an Idiopathic Syringomyelia

机译:初始误诊初始误诊8年后脊柱突瘤的临床形象作为特发性掺入症

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摘要

With the increasing frequency of neuroimaging, incidental intramedullary cavities are diagnosed more frequently. We present a case of asymptomatic incidental intramedullary cervical cavity diagnosed as an idiopathic syringomyelia as initial magnetic resonance imaging (MRI) showed an isolated cystic image without contrasted component. The patient had no subsequent MRI follow-up, but eventually showed symptoms 8 years later. By this stage of the disease, the MRI appearance had changed, showing a solid and enhanced component. The patient underwent surgical resection and histopathology concluded a papillary ependymoma (grade 2). This case illustrates how asymptomatic intramedullary cavities may hide an underlying tumoral process and why these cavities should not be considered as idiopathic syringomyelia by default, except after prolonged MRI follow-up.
机译:随着神经影像学检查频率的增加,偶发性髓腔的诊断率也越来越高。我们报告一例无症状的偶发性颈椎髓内空洞诊断为特发性脊髓空洞症,最初的磁共振成像(MRI)显示一个孤立的囊性图像,没有对比成分。该患者没有后续的MRI随访,但最终在8年后出现症状。到了疾病的这个阶段,MRI的外观已经发生了变化,显示了一个坚实的增强成分。该患者接受了手术切除,组织病理学诊断为乳头状室管膜瘤(2级)。本病例说明了无症状髓内腔如何隐藏潜在的肿瘤过程,以及为什么这些腔在默认情况下不应被视为特发性脊髓空洞症,除非经过长时间的MRI随访。

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