Chatzikomninos Ioannis, Pappa Eleni, Zafeiris Christos P, Zygogiannis Konstantinos, Antonopoulos Spyridon I, Trantos Ioannis Angelos, Kakridonis Fotios, Tsafantakis Emmanouil
Spine and Scoliosis Department, KAT General Hospital, Athens, GRC.
5th Orthopaedic Department, KAT General Hospital, Athens, GRC.
Cureus. 2024 Mar 1;16(3):e55353. doi: 10.7759/cureus.55353. eCollection 2024 Mar.
White cord syndrome is a rare entity, as there are very few cases described in the current literature. Postoperative MRI examination reveals cord intrinsic changes, including edema and ischemia. It is also described as a reperfusion injury of the spinal cord. This report depicts a rare case of "white cord syndrome" with tetraplegia after posterior laminectomy and fusion of the cervical spine in a patient with Klippel-Feil syndrome. A 33-year-old male patient with Klippel-Feil syndrome presented to our department with cervical myelopathy, claudication, deteriorating neurological status, imbalance, and lower limb spasticity. Due to kyphotic malformation of the cervical spine, a two-stage surgical intervention was scheduled. The patient first underwent anterior spinal fusion of C4-C6 with corpectomy of C5, where many anatomical and visceral differentiations were signed, so the surgical team was enhanced by a vascular surgeon. The postoperative period was uneventful and the patient was discharged after a week of hospitalization without any neurological deterioration. A second surgical intervention was scheduled after two months where laminectomy of C5-C7 and posterior fusion of C5-T1 were carried out. However, due to intraoperative spinal instability and various anatomical spinal variations, a third surgery, which would be occipitocervical fusion, was decided as the final surgical solution. During the third surgical operation, after the laminectomy of C1 to C5 and the placement of the occipital plate, the screws, and the two rods in situ, complete nullification of the intraoperative neurophysiologic control was signed. The internal fixation was removed immediately, the wake-up test revealed tetraplegia below C5, and the patient was transferred to the ICU. Immediate MRI revealed no spinal cord hematoma; however, spinal cord edema was present. The patient underwent a tracheostomy and remained quadriplegic with a sensory level of T8 and motor level of C5 and was discharged to a rehabilitation center. The possibility of white cord syndrome should be explained by surgeons before any cervical decompression surgery, as well as a thorough neurological examination should be performed postoperatively. The early recognition and prompt management of white cord syndrome is recommended.
白脊髓综合征是一种罕见的病症,因为目前文献中描述的病例很少。术后MRI检查显示脊髓内部变化,包括水肿和缺血。它也被描述为脊髓的再灌注损伤。本报告描述了一例罕见的“白脊髓综合征”病例,该病例发生在一名患有Klippel-Feil综合征的患者行颈椎后路椎板切除术和融合术后出现四肢瘫痪。一名33岁患有Klippel-Feil综合征的男性患者因颈椎脊髓病、间歇性跛行、神经功能状态恶化、平衡失调和下肢痉挛前来我院就诊。由于颈椎后凸畸形,计划进行两阶段手术干预。患者首先接受了C4-C6前路椎体融合术并切除C5椎体,术中涉及许多解剖和内脏结构的辨别,因此手术团队增加了一名血管外科医生。术后恢复顺利,患者住院一周后出院,无任何神经功能恶化。两个月后安排了第二次手术干预,进行了C5-C7椎板切除术和C5-T1后路融合术。然而,由于术中脊柱不稳定和各种脊柱解剖变异,决定进行第三次手术,即枕颈融合术作为最终手术方案。在第三次手术中,在切除C1至C5椎板并原位放置枕骨板、螺钉和两根棒后,术中神经生理监测完全失效。立即取出内固定物,唤醒试验显示C5以下四肢瘫痪,患者被转入重症监护病房。即刻MRI显示无脊髓血肿;然而,存在脊髓水肿。患者接受了气管切开术,仍四肢瘫痪,感觉平面为T8,运动平面为C5,随后出院至康复中心。在任何颈椎减压手术前,外科医生都应说明白脊髓综合征的可能性,术后也应进行全面的神经学检查。建议对白脊髓综合征进行早期识别和及时处理。