Yokota Kazuya, Kawano Osamu, Kaneyama Hironari, Maeda Takeshi, Nakashima Yasuharu
Department of Orthopaedic Surgery, Japan Labor Health and Welfare Organization Spinal Injuries Center.
Departments of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University, Japan.
Medicine (Baltimore). 2020 May;99(19):e20032. doi: 10.1097/MD.0000000000020032.
Spontaneous spinal subdural hematoma (SSDH) is a rare disease that can cause severe permanent neurological dysfunction. Here we present a case of spontaneous SSDH, in which a series of magnetic resonance images (MRIs) taken through the course of the disease facilitated understanding of the resolution process of the hematoma and the diagnosis of SSDH.
A 59-year-old male presented with sudden severe back pain and rapid onset of paraplegia. This symptom had continued developing while he was transferred to the emergency department. Initial physical examination showed flaccid paralysis of both lower limbs with areflexia and loss of all sensation below T6 bilaterally. MRI images showed an anterior subdural hematoma from C7 to T7 with spinal cord compression.
Based on MRI findings, the diagnosis was SSDH.
We chose conservative treatment of 1-week bed rest and intensive rehabilitation for the patient due to the presence of sacral sparing and the slight motor recovery at 24 hours after the onset.
Frequent MRI images demonstrated that the spinal cord compression was surprisingly mitigated only 2 days and mostly absorbed 4 days after the onset. The patient's motor function was recovered completely and he was discharged after 8 weeks of hospitalization.
Our chronological MRI findings provide crucial information for diagnosing SSDH and also suggest that spinal surgeons should consider the potential option of a conservative approach for treating SSDH. Although prompt selection of a therapeutic strategy for SSDH could be challenging, the surgeons could observe the course of the patient's neurological status for a few days to detect signs of spontaneous recovery.
自发性脊髓硬膜下血肿(SSDH)是一种罕见疾病,可导致严重的永久性神经功能障碍。在此,我们报告一例自发性SSDH病例,在该病例中,通过疾病过程中拍摄的一系列磁共振成像(MRI)有助于理解血肿的消退过程及SSDH的诊断。
一名59岁男性突发严重背痛并迅速出现截瘫。在转至急诊科的过程中,该症状持续发展。初始体格检查显示双下肢弛缓性瘫痪,无反射,双侧T6以下所有感觉丧失。MRI图像显示C7至T7水平硬膜下血肿并伴有脊髓受压。
根据MRI表现,诊断为SSDH。
由于存在骶部感觉保留且发病后24小时有轻微运动恢复,我们为该患者选择了为期1周的卧床休息及强化康复的保守治疗。
频繁的MRI图像显示,发病仅2天后脊髓压迫令人惊讶地减轻,4天后大部分血肿吸收。患者运动功能完全恢复,住院8周后出院。
我们按时间顺序的MRI表现为诊断SSDH提供了关键信息,也提示脊柱外科医生应考虑对SSDH采用保守治疗的潜在选择。尽管为SSDH迅速选择治疗策略可能具有挑战性,但外科医生可以观察患者神经状态几天以发现自发恢复的迹象。