Price Anthony, File Christopher, Call-Orellana Francisco, Andrade de Almeida Romulo Augusto, North Robert Y
John Sealy School of Medicine, The University of Texas Medical Branch at Galveston, Texas.
Department of Neurosurgery, The University of Texas Medical Branch at Galveston, Texas.
J Neurosurg Case Lessons. 2024 Jul 22;8(4). doi: 10.3171/CASE24203.
Paget's disease of bone (PDB) is a common bone metabolic pathology in older adults, characterized by mixed osteolytic, osteoblastic, and quiescent periods. Surgical guidelines for PDB involving the spine are not well-defined and are reserved for cases refractory to medical treatments, typically bisphosphonates like zoledronic acid. This case study describes a 52-year-old male with PDB who presented with rapidly progressing myelopathy symptoms refractory to standard medical treatment, warranting surgical decompression.
Surgical decompression and fusion, involving laminectomy with partial facetectomies, placement of pedicle screw instrumentation, and posterolateral arthrodesis spanning beyond the pathological segment, was performed. Follow-up visits indicated progressive improvement in symptoms and mobility, and imaging showed stable postsurgical changes with increased sclerosis in the affected vertebrae on a 2-year postsurgical course.
This case underscores that PDB of the spine can transition from asymptomatic to significant impairment and demonstrates that surgical intervention can provide effective symptomatic relief in myelopathy secondary to PDB. The case contributes to the growing evidence of the effectiveness of surgical decompression in PDB involving the spine. https://thejns.org/doi/10.3171/CASE24203.
骨Paget病(PDB)是老年人常见的骨代谢疾病,其特征为溶骨期、成骨期和静止期交替出现。涉及脊柱的PDB的手术指南尚不明确,通常适用于对药物治疗(如唑来膦酸等双膦酸盐类药物)无效的病例。本病例研究描述了一名52岁患有PDB的男性,他出现了对标准药物治疗无效的快速进展性脊髓病症状,需要进行手术减压。
进行了手术减压和融合术,包括椎板切除术及部分关节突切除术、椎弓根螺钉内固定置入,以及跨越病变节段的后外侧关节融合术。随访显示症状和活动能力逐渐改善,影像学检查显示在术后2年的病程中,手术部位变化稳定,受累椎体硬化增加。
本病例强调脊柱PDB可从无症状转变为严重功能障碍,并表明手术干预可为PDB继发的脊髓病提供有效的症状缓解。该病例为脊柱PDB手术减压有效性的证据不断增加做出了贡献。https://thejns.org/doi/10.3171/CASE24203 。