Gupta Mayank, Chhabra Harvinder Singh
Department of Spine Surgery, Indian Spinal Injuries Centre, Sector C, Vasant Kunj, Delhi, India, PIN 110070.
Int J Spine Surg. 2020 Jun 30;14(3):391-396. doi: 10.14444/7051. eCollection 2020 Jun.
Fibrocartilaginous embolic myelopathy (FCEM) is a rare cause of spinal cord infarction. It has been confirmed by autopsy in postmortem cases. Herein we describe a case of FCEM diagnosed based on clinical grounds.
A 58-year-old man presented with acute onset of complete paraplegia with bladder and bowel involvement developing a few hours after a trivial trauma. There were no upper motor neuron signs. His magnetic resonance imaging (MRI) was suggestive of longitudinally extensive transverse myelitis from T5 to the conus. There was left paracentral disc protrusion at the T4-T5 level. However, no features of inflammatory, infectious, or autoimmune etiology were found on history, on examination, or in blood or cerebrospinal fluid analysis, and there was no contrast enhancement on MRI.
A diagnosis of anterior spinal artery occlusion was made based on clinical examination with sparing of posterior column sensations in the lower limbs, predominant involvement of anterior half of the spinal cord on MRI, and accompanying new onset of back pain with rapid symptom progression to nadir as opposed to inflammatory etiology. Fibrocartilaginous embolism was suspected after ruling out all other causes of vascular compromise and presence of disc herniation at T4-T5. He was managed with rehabilitation and showed no signs of recovery.
FCEM, though rare, should be kept in mind as a differential diagnosis of acute medical myelopathy when no other cause can be identified.
纤维软骨栓塞性脊髓病(FCEM)是脊髓梗死的一种罕见病因。在尸检病例中已通过尸检得到证实。在此我们描述一例基于临床诊断的FCEM病例。
一名58岁男性,在轻微创伤后数小时出现急性完全性截瘫,并伴有膀胱和肠道功能障碍。无上位运动神经元体征。他的磁共振成像(MRI)提示从T5至圆锥的纵向广泛横贯性脊髓炎。在T4 - T5水平有左旁中央椎间盘突出。然而,在病史、体格检查、血液或脑脊液分析中均未发现炎症、感染或自身免疫病因的特征,且MRI上无强化表现。
基于临床检查,下肢后柱感觉保留,MRI显示脊髓前半部分为主受累,且伴有新发背痛且症状迅速进展至最低点,与炎症病因不同,诊断为脊髓前动脉闭塞。在排除所有其他血管损伤原因及T4 - T5椎间盘突出后,怀疑为纤维软骨栓塞。给予康复治疗,患者无恢复迹象。
FCEM虽罕见,但当无法确定其他病因时,应作为急性脊髓病的鉴别诊断之一予以考虑。