Go Taihei, Tsutsui Toshiyuki, Iida Yasuaki, Fukutake Katsunori, Fukano Ryoichi, Ishigaki Kosei, Tsuchiya Kazuaki, Takahashi Hiroshi
Department of Orthopedic Surgery, Sagamihara Chuo Hospital, Kanagawa, Japan.
Department of Orthopedic Surgery, Toho University, Tokyo, Japan.
Case Rep Orthop. 2019 Mar 13;2019:7384701. doi: 10.1155/2019/7384701. eCollection 2019.
A 76-year-old woman with a spinal subdural hematoma (SDH) was presented with severe back pain without headache. Magnetic resonance imaging (MRI) performed 4 days after onset showed SDH extending from Th2 to L3. She was diagnosed with spontaneous SDH without neurological manifestation, and conservative treatment was selected. Transient disturbance of orientation appeared 7 days after onset. Small subarachnoid hemorrhage (SAH) was detected on head CT, and strict antihypertensive therapy was started. Symptoms changed for the better. Back pain disappeared 4 weeks after onset. On follow-up MRI at 6 months after onset, the SDH had been resolved spontaneously. Although adhesive arachnoiditis was observed at Th4-6, the recurrence of clinical symptoms was not observed at one year and a half after onset. Spinal subdural space is almost avascular; a hematoma in a subdural space is considered to come from a subarachnoid space when it is a lot. A hemorrhage in subarachnoid space was flushed by cerebral spinal fluid; hematoma or arachnoiditis was not formed in general. In our case, hemorrhage was a lot and expansion of SDH was large enough to cause cranial SAH and arachnoiditis. But longitudinally expanded SDH did not show neurological manifestation and resolved spontaneously in our case.
一名76岁患有脊髓硬膜下血肿(SDH)的女性,表现为严重背痛但无头痛。发病4天后进行的磁共振成像(MRI)显示SDH从胸2延伸至腰3。她被诊断为无神经表现的自发性SDH,并选择了保守治疗。发病7天后出现短暂的定向障碍。头部CT检测到小的蛛网膜下腔出血(SAH),并开始严格的降压治疗。症状好转。发病4周后背痛消失。发病6个月后的随访MRI显示SDH已自发消退。虽然在胸4 - 6观察到粘连性蛛网膜炎,但发病一年半后未观察到临床症状复发。脊髓硬膜下间隙几乎无血管;当硬膜下间隙有大量血肿时,认为其来源于蛛网膜下腔。蛛网膜下腔出血被脑脊液冲走;一般不会形成血肿或蛛网膜炎。在我们的病例中,出血量大且SDH扩展范围大到足以导致颅内SAH和蛛网膜炎。但在我们的病例中,纵向扩展的SDH未显示神经表现且自发消退。