Baldwin Avionna, Mesfin Addisu
Department of Orthopaedic Surgery, University of Rochester Medical Center, Rochester, NY 14642, USA.
Department of Orthopaedic Surgery, University of Rochester Medical Center, Rochester, NY 14642, USA.
Spine Deform. 2017 Nov;5(6):435-439. doi: 10.1016/j.jspd.2017.04.006.
Case report.
To report the clinical and imaging findings of a patient with lumbar stenosis 44 years after posterior spinal fusion for congenital lumbar kyphosis.
To our knowledge, there are no long-term follow-up reports after posterior spine fusion (PSF) for congenital kyphosis. Congenital kyphosis is an uncommon deformity with the potential to progress rapidly and result in deformity and neurologic deficits.
We report the patient's history, physical examination, imaging findings, and management in addition to providing a literature review.
A 54-year-old-male who underwent T8-L3 PSF in 1972 because of congenital kyphosis presented 44 years after surgery with lower back pain, buttock, and bilateral posterior leg pain. On physical examination, no weakness was elicited and magnetic resonance imaging demonstrated L4-L5 lumbar stenosis. The patient was enrolled in physical therapy and responded well to medical/interventional management.
To our knowledge, this is the longest follow-up of surgical management of congenital lumbar kyphosis. Posterior fusion only halted the progression of the kyphosis with subsequent developed of adjacent segment disease distal to the fusion.
Level IV.
病例报告。
报告一名先天性腰椎后凸患者在脊柱后路融合术后44年出现腰椎管狭窄的临床及影像学表现。
据我们所知,尚无先天性后凸脊柱后路融合术(PSF)的长期随访报告。先天性后凸是一种罕见的畸形,有迅速进展并导致畸形和神经功能缺损的可能。
我们报告该患者的病史、体格检查、影像学表现及治疗情况,并进行文献综述。
一名54岁男性,1972年因先天性后凸接受T8-L3脊柱后路融合术,术后44年出现下背部疼痛、臀部及双侧下肢后侧疼痛。体格检查未引出肌力减弱,磁共振成像显示L4-L5腰椎管狭窄。该患者接受了物理治疗,对药物/介入治疗反应良好。
据我们所知,这是先天性腰椎后凸手术治疗最长的随访。后路融合仅阻止了后凸的进展,但随后在融合节段远端出现了相邻节段疾病。
四级。