Paisan Gabriella M, Buell Thomas J, Raper Daniel, Asthagiri Ashok
Department of Neurosurgery, University of Virginia, Charlottesville, Virginia, USA.
Department of Neurosurgery, University of Virginia, Charlottesville, Virginia, USA.
World Neurosurg. 2017 Dec;108:993.e13-993.e17. doi: 10.1016/j.wneu.2017.08.189. Epub 2017 Sep 7.
Spinal subdural hematomas (SSDHs) are rare and usually associated with bleeding diatheses, trauma, iatrogenic injury, spinal vascular malformations, or intraspinal tumors.
We report a case of a 75-year-old man who developed a symptomatic lumbosacral SSDH after undergoing resection of a right temporal glioblastoma multiforme. The patient subsequently recovered and was discharged home. Over the next 2 weeks, he developed progressively worsening symptoms of lower back pain, lower extremity weakness, and urinary retention. Although the patient had no known risk factors for developing a SSDH, magnetic resonance imaging on postoperative day 16 revealed an extensive L2-sacrum SSDH. The patient underwent L2-L5 total laminectomies for evacuation of the SSDH. His symptoms resolved after surgery. Literature review produced 26 other cases of SSDHs after intracranial surgery in patients without obvious risk factors. In our case, the lumbosacral SSDH may have originated from downward migration of intracranial blood in a gravity-dependent fashion. Radiographic evidence of blood within the posterior thecal sac of the patient's cervical spine supports this hypothesis.
In most cases, SSDHs after intracranial surgery resolve with conservative treatment; however, as shown in our case, surgery may be required if there is progressive neurologic decline. Neurosurgeons should be aware of this potential complication after intracranial surgery; a magnetic resonance imaging of the spine may be indicated if there is unexplained lower extremity pain or weakness.
脊髓硬膜下血肿(SSDHs)较为罕见,通常与出血性疾病、创伤、医源性损伤、脊髓血管畸形或脊髓内肿瘤有关。
我们报告一例75岁男性,在接受右侧颞叶多形性胶质母细胞瘤切除术后出现有症状的腰骶部SSDH。患者随后康复并出院回家。在接下来的2周内,他出现了逐渐加重的下背部疼痛、下肢无力和尿潴留症状。尽管该患者没有已知的发生SSDH的危险因素,但术后第16天的磁共振成像显示广泛的L2 - 骶骨SSDH。患者接受了L2 - L5全椎板切除术以清除SSDH。术后他的症状得到缓解。文献回顾发现另外26例无明显危险因素的患者在颅内手术后发生SSDH的病例。在我们的病例中,腰骶部SSDH可能是以重力依赖方式由颅内血液向下迁移所致。患者颈椎硬膜囊后部内血液的影像学证据支持这一假设。
在大多数情况下,颅内手术后的SSDH通过保守治疗可缓解;然而,如我们的病例所示,如果出现进行性神经功能衰退,可能需要手术治疗。神经外科医生应意识到颅内手术后这种潜在并发症;如果出现无法解释的下肢疼痛或无力,可能需要进行脊柱磁共振成像检查。