Patnaik Ashis, Mishra Sudhansu S, Mishra Sanjib, DAS Srikanta, Deo Rama C
Scb Medical College, Department of Neurosurgery, Orissa, India.
Turk Neurosurg. 2014;24(2):253-5. doi: 10.5137/1019-5149.JTN.5595-11.2.
We report a case of ganglioneuroblastoma of the spinal cord in a 25-year-old man. Clinical history was short with paraparesis and bladder involvement. The MRI picture was that of an extradural solid tumor with extension to both intervertebral foramina, more suggestive of nerve sheath tumour rather than malignant embryonal tumour. Diagnosis was established by histopathological study. We could not find such a presentation of spinal ganglioneuroblastoma as an extradural, primary tumour in the literature. We discuss the radio-pathological features, surgical management and post-operative outcome.
我们报告一例25岁男性脊髓神经节神经母细胞瘤。临床病史较短,伴有双下肢轻瘫和膀胱受累。MRI表现为硬膜外实性肿瘤,延伸至双侧椎间孔,更提示神经鞘瘤而非恶性胚胎性肿瘤。通过组织病理学研究确诊。我们在文献中未发现脊髓神经节神经母细胞瘤以硬膜外原发性肿瘤形式出现的此类病例。我们讨论了其放射病理学特征、手术治疗及术后结果。