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在影像学显示成功的人体椎间融合器中骨移植融合情况

Bone graft incorporation in radiographically successful human intervertebral body fusion cages.

作者信息

Togawa D, Bauer T W, Brantigan J W, Lowery G L

机构信息

Department of Anatomic Pathology, Cleveland Clinic Foundation, Ohio 44195, USA.

出版信息

Spine (Phila Pa 1976). 2001 Dec 15;26(24):2744-50. doi: 10.1097/00007632-200112150-00025.

Abstract

STUDY DESIGN

Biopsies were obtained from within radiographically successful human intervertebral body fusion cages to document the histology of remodeling bone graft.

OBJECTIVES

The purpose of this study is to describe the tissue within successful human interbody cages with special reference to the viability of bone and the presence or absence of debris particles.

SUMMARY OF BACKGROUND DATA

The use of interbody fusion cages is gaining rapid acceptance, but there is little histologic documentation of the nature of tissue within successful human interbody fusion cages.

METHODS

Needle biopsies were obtained of tissue within radiographically successful intervertebral body fusion cages at the time of pedicle screw removal for back pain or fusion of adjacent spinal level in nine spinal levels of eight patients. Preoperative diagnoses of these eight adult patients included disease conditions in the sagittal plane: spondylosis (5), degenerative disc disease (6), failed laminectomy and discectomy (2), radiculopathy (1), and spondylolisthesis (1). In all cases the cages had been packed with autograft (iliac crest 7, local 1) at the time of insertion. Cage implantation was performed with anterior (anterior lumbar interbody fusion 4, corpectomy and plate fixation 1), and posterior (posterior lumbar interbody fusion 4), segmental instrumentation (plate 1, or pedicle screws 8). All cases except one cervical case had posterolateral fusion or bilateral facet fusion. The cages were composed of carbon fiber-reinforced polymer (Brantigan cage; DePuy AcroMed, Raynham, MA, n = 5) or titanium mesh (Harms Cage; DePuy AcroMed, Raynham, MA, n = 4). Cages had been in situ from 8 to 72 months (mean 28 months). All nine biopsies from eight patients were obtained from within the center of the cages. Specimens were decalcified, routinely embedded in paraffin, stained with hematoxylin and eosin, and viewed qualitatively with transmitted and polarized light.

RESULTS

All needle biopsies were obtained from within the center of the cages, and no patient developed spinal instability after the biopsy. All nine biopsies showed small fragments of necrotic bone associated with viable bone and restoration of hematopoietic bone marrow. Numerous cement lines demarcated the edges of previous cycles of remodeling. The ratio of necrotic to viable bone varied greatly among cases. Small particles of debris were associated with four of the five carbon-fiber cages and one of the four specimens from titanium cages, but there was no visible bone resorption or inflammation.

CONCLUSIONS

Autogenous bone graft was incorporated in these radiographically successful human intervertebral body fusion cages. A few debris particles were observed, but there was no histologic evidence of particle-induced bone resorption or inflammation.

摘要

研究设计

从影像学检查显示成功的人体椎间融合器内获取活检组织,以记录移植骨重塑的组织学情况。

目的

本研究旨在描述成功的人体椎间融合器内的组织,特别关注骨的活力以及是否存在碎片颗粒。

背景资料总结

椎间融合器的应用正在迅速得到认可,但关于成功的人体椎间融合器内组织性质的组织学记录很少。

方法

在8例患者的9个脊柱节段因背痛或相邻节段融合而取出椎弓根螺钉时,从影像学检查显示成功的椎间融合器内获取针吸活检组织。这8例成年患者的术前诊断包括矢状面疾病情况:脊柱退变(5例)、椎间盘退变疾病(6例)、椎板切除和椎间盘切除失败(2例)、神经根病(1例)和脊椎滑脱(1例)。所有病例在植入时椎间融合器均已填充自体骨(髂嵴骨7例,局部骨1例)。采用前路(前路腰椎椎间融合术4例,椎体次全切除及钢板固定1例)和后路(后路腰椎椎间融合术4例)节段性内固定(钢板1例,或椎弓根螺钉8例)进行椎间融合器植入。除1例颈椎病例外,所有病例均行后外侧融合或双侧小关节融合。椎间融合器由碳纤维增强聚合物(Brantigan融合器;DePuy AcroMed公司,马萨诸塞州雷纳姆,n = 5)或钛网(Harms融合器;DePuy AcroMed公司,马萨诸塞州雷纳姆,n = 4)制成。融合器在位时间为8至72个月(平均28个月)。8例患者的9份活检组织均取自融合器中心。标本经脱钙处理,常规石蜡包埋,苏木精-伊红染色,并用透射光和偏振光进行定性观察。

结果

所有针吸活检组织均取自融合器中心,活检后无患者出现脊柱不稳定。所有9份活检组织均显示有与存活骨相关的坏死骨小碎片以及造血骨髓的恢复。大量骨水泥线界定了先前重塑周期的边缘。坏死骨与存活骨的比例在各病例中差异很大。5个碳纤维融合器中的4个以及4个钛网融合器标本中的1个有小碎片颗粒,但未见明显的骨吸收或炎症。

结论

自体骨移植已融入这些影像学检查显示成功的人体椎间融合器中。观察到少量碎片颗粒,但无组织学证据表明颗粒引起骨吸收或炎症。

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