Cassidy R Carter, Shaffer William O
University of Kentucky Medical Center, K-401, Kentucky Clinic, 740 South Limestone Street, Lexington, KY 40536, USA.
Spine J. 2008 Jul-Aug;8(4):691-5. doi: 10.1016/j.spinee.2007.04.005. Epub 2007 May 22.
Congenital insensitivity to pain is a rare disorder that can lead to neuropathic arthropathy of any joint including the spine. Most of the case reports in the literature are in the pediatric population.
This case report emphasizes the importance of anterior and posterior fusion in patients with congenital insensitivity to pain. The patient was initially treated as if the deformity was postinfectious. STUDY DESIGN SETTING: The patient was treated in a university-based tertiary care center.
The patient underwent an anterior decompression and fusion with instrumentation that failed with ambulation. An anterior and posterior revision with instrumentation was then performed to stabilize the Charcot spine.
The patient had an excellent final outcome. At 2 years postoperatively, he is solidly fused and back to his normal occupation.
Anterior and posterior fusion is essential in neuropathic spinal arthropathy. Congenital insensitivity to pain can manifest problems into adulthood.
先天性无痛觉是一种罕见的疾病,可导致包括脊柱在内的任何关节发生神经性关节病。文献中的大多数病例报告都来自儿科人群。
本病例报告强调了先天性无痛觉患者前后路融合的重要性。该患者最初被当作感染后畸形进行治疗。研究设计与背景:该患者在一家大学附属三级护理中心接受治疗。
患者接受了前路减压及器械辅助融合术,但术后行走时手术失败。随后进行了前后路翻修及器械辅助固定术以稳定夏科氏脊柱。
患者最终获得了良好的疗效。术后2年,他实现了牢固融合并重返正常工作岗位。
前后路融合术在神经性脊柱关节病中至关重要。先天性无痛觉可在成年期出现问题。