Singh Suyash, Bhaisora Kamlesh Singh, Sardhara Jayesh, Das Kuntal Kanti, Attri Gagandeep, Mehrotra Anant, Srivastava Arun Kumar, Jasiwal Awadesh Kumar, Behari Sanjay
Department of Neurosurgery, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
J Craniovertebr Junction Spine. 2019 Jan-Mar;10(1):64-71. doi: 10.4103/jcvjs.JCVJS_12_19.
Spinal arachnoid cyst is an uncommon entity, presenting with radiculopathy or paraparesis. These cysts are usually found in intradural extramedullary region; and the extradural region is a rare location. The exact pathogenesis in the existence of these cysts in the extradural region is still debated. In this article, we have retrospectively analyzed the clinical profile of the rare extradural arachnoid cyst (EDAC).
In this study, 19 patients of EDAC operated at our institute between January 2006 to June 2016 are analyzed. All patients with the Oswestry disability index score of >20 were managed surgically (open laminectomy and cyst excision). The clinical outcome was assessed at using 5-point satisfaction scale and McCormick grading.
All 13 operated patients had EDACs with communication with the intradural compartment. In 11 (84.6%) patients, cyst wall was excised completely, in 2 (15.3%) patients underwent partial excision of cyst wall; dural communication was closed in all patients ( = 13). None of the patients had clinical deterioration or radiological recurrence till the last follow-up. Mean follow-up was 52.2 months (range 1-160); all patients were satisfied after surgery (median score was 3).
Symptomatic EDACs account <2% of all spinal tumors. The EDACs have communication with the intradural compartment. In our article, we have discussed the approach and management of EDAC, including minimally invasive percutaneous procedures.
One should aim for preoperative or intraoperative localization of dural communication and try to disconnect the extradural cyst from the intradural connection to prevent recurrence. Surgical treatment is complete excision of the cyst.
脊髓蛛网膜囊肿是一种罕见的疾病,表现为神经根病或轻截瘫。这些囊肿通常位于硬脊膜内髓外区域;而硬脊膜外区域则是罕见的发病部位。硬脊膜外区域存在这些囊肿的确切发病机制仍存在争议。在本文中,我们回顾性分析了罕见的硬脊膜外蛛网膜囊肿(EDAC)的临床特征。
在本研究中,对2006年1月至2016年6月期间在我院接受手术的19例EDAC患者进行了分析。所有奥斯威斯功能障碍指数评分>20的患者均接受手术治疗(开放性椎板切除术和囊肿切除术)。使用5分满意度量表和麦考密克分级法评估临床结果。
所有13例接受手术的患者均患有与硬脊膜内腔相通的EDAC。11例(84.6%)患者的囊肿壁被完全切除,2例(15.3%)患者接受了囊肿壁部分切除;所有患者(n = 13)的硬脊膜相通处均被封闭。直到最后一次随访,所有患者均未出现临床病情恶化或影像学复发。平均随访时间为52.2个月(范围1 - 160个月);所有患者术后均感到满意(中位数评分为3分)。
有症状的EDAC占所有脊柱肿瘤的比例<2%。EDAC与硬脊膜内腔相通。在我们的文章中,我们讨论了EDAC的治疗方法,包括微创经皮手术。
应在术前或术中对硬脊膜相通处进行定位,并尝试将硬脊膜外囊肿与硬脊膜内连接断开,以防止复发。手术治疗是完全切除囊肿。