Jain Viral V, Anadio Jennifer M, Chan Gilbert, Sturm Peter F, Crawford Alvin H
*Cincinnati Children's Hospital Medical Center, Cincinnati, OH †Kosair Children's Hospital, Children's Orthopedics of Louisville, Louisville, KY.
J Pediatr Orthop. 2014 Oct-Nov;34(7):e44-9. doi: 10.1097/BPO.0000000000000186.
We present a case of an incidental finding of dural ectasia in a child diagnosed with Larsen syndrome. Larsen syndrome is a rare inherited disorder of connective tissue characterized by facial dysmorphism, congenital joint dislocations of the hips, knees and elbows, and deformities of the hands and feet. Dural ectasia is as an abnormal expansion of the dural sac surrounding the spinal cord and may result in spinal morphologic changes, instability, and spontaneous dislocation. To the best of our knowledge, the presence of dural ectasia in Larsen syndrome has not previously been reported.
A 6-year-old boy diagnosed with Larsen syndrome presented with an upper thoracic curve measuring 74 degrees, a right thoracic curve measuring 65 degrees, and significant cervicothoracic kyphosis with 50% anterior subluxation of C6 on C7 and C7 on T1. Advanced imaging studies showed dural ectasia (evidenced by spinal canal and dural sac expansion), thinning of pedicles and lamina, and C4 and C6 pars defects with cervical foramen enlargement. The patient received growing rod instrumentation (attached to cervical spine fixation) by a combined anterior/posterior surgical approach using intraoperative halo. Complications included intraoperative medial breach (fully resolved), wound dehiscence, 2 instances of bilateral broken rods, and a broken cervical rod. Following 7 lengthening procedures, the patient underwent definitive fusion.
Surgeons should be aware of the potential for dural ectasia in patients with Larsen syndrome. Its presence will cause difficulties in the surgical intervention for spinal deformity. Multiple factors must be considered, and surgical approach and technique will require modification to avoid complications. Although dural ectasia confounds surgical intervention in these patients, surgery still appears to outweigh the risks associated with delayed intervention. The presence of dural ectasia should not preclude surgical decompression and stabilization. This report adds to the body of knowledge on the treatment of Larsen syndrome by demonstrating the potential existence of dural ectasia and highlights the importance of careful and thorough preoperative evaluation and diagnostic imaging.
我们报告一例在诊断为拉森综合征的儿童中偶然发现硬脊膜扩张的病例。拉森综合征是一种罕见的遗传性结缔组织疾病,其特征为面部畸形、髋、膝和肘关节先天性脱位以及手足畸形。硬脊膜扩张是指脊髓周围硬脊膜囊的异常扩张,可能导致脊柱形态改变、不稳定和自发性脱位。据我们所知,此前尚未有关于拉森综合征中存在硬脊膜扩张的报道。
一名诊断为拉森综合征的6岁男孩,其胸上段侧弯角度为74度,胸右段侧弯角度为65度,并有明显的颈胸段后凸,C6相对于C7以及C7相对于T1向前半脱位50%。高级影像学检查显示硬脊膜扩张(表现为椎管和硬脊膜囊扩张)、椎弓根和椎板变薄,以及C4和C6椎弓根峡部缺损伴颈椎椎间孔扩大。患者通过术中使用头环的前后联合手术方法接受了生长棒内固定术(连接颈椎固定装置)。并发症包括术中内侧破裂(已完全恢复)、伤口裂开、2次双侧棒断裂以及1次颈椎棒断裂。经过7次延长手术后,患者接受了确定性融合手术。
外科医生应意识到拉森综合征患者存在硬脊膜扩张的可能性。其存在会给脊柱畸形的手术干预带来困难。必须考虑多种因素,并且手术入路和技术需要进行调整以避免并发症。尽管硬脊膜扩张给这些患者的手术干预带来了困扰,但手术似乎仍比延迟干预带来的风险更可取。硬脊膜扩张的存在不应排除手术减压和稳定治疗。本报告通过证明硬脊膜扩张的潜在存在,增加了关于拉森综合征治疗的知识体系,并强调了仔细全面的术前评估和诊断性影像学检查的重要性。