Zhang Liang, Qiao Guangyu, Shang Aijia, Yu Xinguang
Medical School of Nankai University, No. 94, Weijin Road, Naikai District, Tianjin 300071, Tianjin, People's Republic of China; Department of Neurosurgery, Chinese PLA General Hospital, No. 28, Fuxing Road, Haidian District, Beijing 100853, People's Republic of China.
Department of Neurosurgery, Chinese PLA General Hospital, No. 28, Fuxing Road, Haidian District, Beijing 100853, People's Republic of China.
J Clin Neurosci. 2020 Jul;77:25-30. doi: 10.1016/j.jocn.2020.05.052. Epub 2020 May 23.
Spinal dural arteriovenous fistula (dAVF) is an extremely rare vascular entity that is usually misdiagnosed. We sought to determine the long-term clinical outcomes of patients undergoing microsurgical treatment for delayed diagnosis of spinal dAVF. This retrospective study identified patients with delayed diagnosed spinal dAVF at our institution from 2009 to 2018. Patients' data, including demographics, imaging, and follow-up data, were evaluated. This cohort included 65 consecutive patients with 68 dAVFs and a male-to-female ratio of 4:1 and a mean age of 53.5 ± 13.7 years. The presenting symptoms consisted of limb weakness (n = 42, 64.6%), paraparesis (n = 34, 52.3%), sphincter disturbances (n = 8, 12.3%), and pain (n = 13, 20.0%). The proportion of patients with each symptom significantly increased and patients experienced increased disability when the diagnosis was finalized. The mean length of delay of diagnosis was 20.7 ± 30.0 months. Surgery resulted in complete occlusion of the fistula on the first attempt in all patients. Three patients developed recurrent fistulas, and three died in the follow-up period. Improved motor function was achieved in 38 patients (59.5%). Other symptoms, such as sensory disorders, sphincter dysfunction, and pain, improved by 37.3%, 32.3%, and 66.7%, respectively. Patients with spinal dAVF usually exhibit progressive ascending myelopathy and often remain misdiagnosed for months to years. Some patients' increased disability cannot be reversed through surgery.
脊髓硬脊膜动静脉瘘(dAVF)是一种极其罕见的血管病变,通常会被误诊。我们试图确定因脊髓dAVF诊断延迟而接受显微外科治疗的患者的长期临床结局。这项回顾性研究确定了2009年至2018年在我们机构中诊断延迟的脊髓dAVF患者。对患者的数据进行了评估,包括人口统计学、影像学和随访数据。该队列包括65例连续患者,共68个dAVF,男女比例为4∶1,平均年龄为53.5±13.7岁。主要症状包括肢体无力(n = 42,64.6%)、双下肢轻瘫(n = 34,52.3%)、括约肌功能障碍(n = 8,12.3%)和疼痛(n = 13,20.0%)。当最终确诊时,每种症状的患者比例显著增加,患者的残疾程度也有所加重。诊断延迟的平均时长为20.7±30.0个月。手术使所有患者的瘘管在首次尝试时即完全闭塞。3例患者出现复发性瘘管,3例在随访期间死亡。38例患者(59.5%)的运动功能得到改善。其他症状,如感觉障碍、括约肌功能障碍和疼痛,分别改善了37.3%、32.3%和66.7%。脊髓dAVF患者通常表现为进行性上升性脊髓病,且常常在数月至数年的时间里一直被误诊。一些患者增加的残疾程度无法通过手术逆转。