Nguyen Ha Son, Lozen Andrew, Doan Ninh, Gelsomin Michael, Shabani Saman, Maiman Dennis
Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, USA.
J Craniovertebr Junction Spine. 2015 Oct-Dec;6(4):219-22. doi: 10.4103/0974-8237.167887.
Dural ectasia is frequently associated with connective tissue disorders or inflammatory conditions. Presentation in a patient without known risk factors is rare. Moreover, the literature regarding the treatment options for symptomatic dural ectasia is controversial, variable, and limited. A 62-year-old female presents with intractable, postural headaches for years. A lumbar puncture revealed opening pressure 3 cm of water. A computed tomography myelogram of the spine demonstrated erosion of her sacrum due to a large lumbosacral dural ectasia. An initial surgery was attempted to reduce the size of the expansile dura, and reconstruct the dorsal sacrum with a titanium plate (Depuy Synthes, Westchester, PA, USA) to prevent recurrence of thecal sac dilatation. Her symptoms initially improved, but shortly thereafter recurred. A second surgery was then undertaken to obliterate the thecal sac distal to the S2 nerve roots. This could not be accomplished through simple ligation of the thecal sac circumferentially as the ventral dura was noted to be incompetent and attempts to develop an extradural tissue plane were unsuccessful. Consequently, an abundance of fibrin glue was injected into the thecal sac distal to S2, and the dural ectasia was marsupialized rostrally, effectively obliterating the distal thecal sac while further reducing the size of the expansile dura. This approach significantly improved her symptoms at 5 months follow-up. Treatment of dural ectasia is not well-defined and has been variable based on the underlying manifestations. We report a rare patient without risk factors who presented with significant lumbosacral dural ectasia. Moreover, we present a novel method to treat postural headaches secondary to dural ectasia, where the thecal sac is obliterated distal to the S2 nerve roots using an abundance of fibrin glue followed by marsupialization of the thecal sac rostally. This method may offer an effective therapy option as it serves to limit the expansile dura, reducing the cerebrospinal fluid sump and the potential for intracranial hypotension.
硬脊膜扩张症常与结缔组织疾病或炎症性疾病相关。在无已知危险因素的患者中出现这种情况较为罕见。此外,关于有症状的硬脊膜扩张症的治疗选择,文献存在争议、各不相同且有限。一名62岁女性多年来一直患有顽固性体位性头痛。腰椎穿刺显示初压为3厘米水柱。脊柱计算机断层扫描脊髓造影显示,由于巨大的腰骶部硬脊膜扩张症,她的骶骨受到侵蚀。最初尝试进行手术以减小扩张硬脊膜的大小,并用钛板(美国宾夕法尼亚州韦斯特切斯特的Depuy Synthes公司生产)重建骶骨背侧,以防止硬膜囊扩张复发。她的症状最初有所改善,但不久后又复发了。随后进行了第二次手术,以闭塞S2神经根远端的硬膜囊。由于发现腹侧硬脊膜功能不全,无法通过简单地环形结扎硬膜囊来完成,并且试图形成硬膜外组织平面也未成功。因此,向S2远端的硬膜囊内注入了大量纤维蛋白胶,并将硬脊膜扩张症向头侧袋形缝合,有效地闭塞了远端硬膜囊,同时进一步减小了扩张硬脊膜的大小。这种方法在5个月的随访中显著改善了她的症状。硬脊膜扩张症的治疗尚无明确的定义,且因潜在表现而异。我们报告了一名无危险因素但出现明显腰骶部硬脊膜扩张症的罕见患者。此外,我们提出了一种治疗硬脊膜扩张症继发体位性头痛的新方法,即使用大量纤维蛋白胶闭塞S2神经根远端的硬膜囊,然后将硬膜囊向头侧袋形缝合。这种方法可能提供一种有效的治疗选择,因为它有助于限制扩张的硬脊膜,减少脑脊液池和颅内低压的可能性。