Baruah Satyakam, Dubey Sudhir, Ghavghave Utkarsh, Jha Ajaya Nand
Department of Neurosurgery, Institute of Neurosciences, Medanta the Medicity, Gurgaon, Haryana, India.
Department of Neurosurgery, Institute of Neurosciences, Medanta the Medicity, Gurgaon, Haryana, India.
World Neurosurg. 2019 Feb;122:272-277. doi: 10.1016/j.wneu.2018.10.201. Epub 2018 Nov 4.
Neurologic complications are increasingly being reported in dengue epidemics. Intraspinal hematomas are rare, and those associated with dengue fever are still rarer with only 1 being reported in the literature.
We report a case of dengue fever presenting with acute-onset quadriparesis (upper limbs Medical Research Council [MRC] 4/5 and lower limbs 0/5) and urinary incontinence. The patient was radiologically diagnosed with cervicodorsal acute to subacute anterior epidural hematoma. On the basis of clinical and radiologic evaluations, the patient underwent an anterior cervical approach via a split-manubriotomy, C6-D4 right anterolateral partial oblique corpectomies for evacuation of the hematoma. Intraoperatively, however, there was no evidence of anterior epidural collection and the dura revealed a bluish hue. A durotomy revealed a subdural hematoma. After evacuation of the hematoma, the patient remained paraplegic and her upper limb power worsened by MRC 1 grade. Postoperative magnetic resonance imaging revealed good evacuation and no new bleed; however, the intramedullary T2-weighted signal hyperintensities extending up to C2 persisted. She was on ventilatory support for almost 5 months. For diaphragmatic incapacity she underwent bilateral cervical phrenic nerve stimulation (diaphragmatic pacing). Despite initial improvement, she succumbed to multiple underlying comorbidities.
Acute spontaneous spinal subdural hematoma (SSDH) is extremely rare but should be kept in mind in patients with dengue hemorrhagic fever. The radiologic findings could be deceptive and plain computed tomography and magnetic resonance imaging should be used as complementary studies to establish the diagnosis of acute spontaneous SSDH. The outcomes of SSDH are guarded, and elaborate patient counseling should be done preoperatively, keeping these in perspective.
登革热流行期间,神经系统并发症的报道日益增多。脊髓内血肿较为罕见,与登革热相关的则更为罕见,文献中仅报道过1例。
我们报告1例登革热患者,出现急性四肢瘫(上肢医学研究委员会[MRC]肌力4/5,下肢0/5)及尿失禁。患者经影像学检查诊断为颈胸段急性至亚急性硬膜外血肿。基于临床和影像学评估,患者通过劈开胸骨入路行前路颈椎手术,进行C6 - D4右侧前外侧部分斜行椎体次全切除以清除血肿。然而,术中未发现硬膜外血肿,硬膜呈蓝色。切开硬膜后发现硬膜下血肿。清除血肿后,患者仍截瘫,上肢肌力下降1级。术后磁共振成像显示血肿清除良好且无新出血;然而,延至C2水平的髓内T2加权像信号高增强持续存在。她接受了近5个月的通气支持。因膈肌功能不全,她接受了双侧颈膈神经刺激(膈肌起搏)。尽管最初有改善,但她最终因多种基础合并症死亡。
急性自发性脊髓硬膜下血肿(SSDH)极为罕见,但在登革出血热患者中应予以考虑。影像学表现可能具有欺骗性,应使用平扫计算机断层扫描和磁共振成像作为辅助检查以明确急性自发性SSDH的诊断。SSDH的预后不佳,术前应详细向患者说明情况,并考虑到这些因素。