Department of Neurological Surgery, Oregon Health & Science University, Portland, Oregon 97239, USA.
Neurosurgery. 2009 Dec;65(6):1161-4; discussion 1164-5. doi: 10.1227/01.NEU.0000359223.11215.D9.
Spinal catheter granulomas are a rare and, most likely, underreported complication of intrathecal opioid therapy. Such granulomas can be associated with devastating neurological sequelae if not treated in a timely fashion. Most neurosurgeons, however, are unlikely to have had experience in the surgical management of this condition.
The authors present 3 surgical cases of patients with spinal catheter granulomas with neurological deficits. One patient's intraoperative video illustrates the challenges of diagnosis, radiological assessment, and surgery for spinal catheter granulomas.
All 3 patients had implanted opioid pumps for management of chronic spinal pain secondary to fracture, tethered cord, and back pain. Increasing back pain and a progressive myelopathy was observed in all patients. A clear radiological diagnosis was made more difficult because of instrumentation artifact in 1 case and claustrophobia in another. Computed tomographic myelography was necessary in 1 case. The surgical findings were: 1 extradural catheter with granuloma and 2 intradural catheters encased with granuloma and adherent to the cord. The extradural catheter was trimmed of granuloma and replaced intradurally in 1 case. The patients with intradural catheter granulomas required judicious dissection of the granulomas from the dorsum of the cord, duroplasty, and catheter section. Critical intraoperative stages were recorded and are presented in digital movie format. Two patients had neurological improvement after surgery; however, 1 patient remained paraplegic. The 2 patients with catheter section required opioid withdrawal treatment.
The operative management of spinal intrathecal granulomas associated with opioid infusion pumps can be challenging and depends on a high degree of clinical suspicion, imaging results, and operative findings.
椎管内导管肉芽肿是鞘内阿片类药物治疗的一种罕见且极有可能被低估的并发症。如果不及时治疗,此类肉芽肿可能会导致严重的神经后遗症。然而,大多数神经外科医生可能没有处理这种情况的手术经验。
作者介绍了 3 例因脊髓导管肉芽肿导致神经功能缺损的手术病例。1 例患者的术中视频说明了诊断、影像学评估和治疗脊髓导管肉芽肿的挑战。
所有 3 例患者均因骨折、脊髓栓系和腰痛导致慢性脊髓疼痛而植入阿片类药物输注泵。所有患者均出现背痛加重和进行性脊髓病。1 例因器械伪影和另 1 例因幽闭恐惧症使明确的放射学诊断变得更加困难。1 例需要进行 CT 脊髓造影。手术发现:1 例硬膜外导管伴肉芽肿,2 例硬膜内导管被肉芽肿包裹并与脊髓粘连。1 例患者将带肉芽肿的硬膜外导管修剪后重新植入硬膜内。对于有硬膜内导管肉芽肿的患者,需要从脊髓背侧谨慎分离肉芽肿、硬脑膜成形术和导管分段。记录了关键的手术阶段并以数字电影格式呈现。2 例患者术后神经功能改善,1 例仍截瘫。2 例需要进行导管分段的患者需要进行阿片类药物戒断治疗。
与输注泵相关的脊髓内鞘内肉芽肿的手术治疗具有挑战性,取决于高度的临床怀疑、影像学结果和手术发现。