急性和亚急性骨质疏松椎体骨折不同愈合时期骨组织形态学分析
Bone histomorphologic analysis at different healing stages of sub and acute osteoporotic vertebral fracture
  
DOI:10.3969/j.issn.1006-7108.2020.12.018
中文关键词:  骨质疏松性椎体压缩骨折  活检  骨组织形态计量学
英文关键词:osteoporotic vertebral compression fracture  biopsy  bone histomorphometry
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作者单位
张芸1 齐浩然2 高观4 姜强4 王磊 3 王文波3 孙建民2 王均宁1 薛景才3* 1.山东中医药大学中医学院 山东 济南 250012 2.山东大学附属省立医院 山东 济南 250012 3.山东中医药大学第二附属医院脊柱外科山东 济南 250012 4.山东省威海卫人民医院脊柱外科山东威海 261002 
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中文摘要:
      目的 观察急性和亚急性骨质疏松性椎体压缩骨折(osteoporotic vertebral compression fracture,OVCF)发生后,不同愈合时期椎体内骨组织病理特点。方法 将119例(OVCF)患者按发病时间分为四期:I期(0~15 d);II期(15~30 d);III期(30~60 d);IV期(60~90 d)。常规行椎体内骨折区活检骨组织取出,制备脱钙活检标本,运用光镜观察并骨组织形态计量学分析。结果 共获得活检标本119例,其中I期67例(56.3 %)、II期28例(23.5 %)、III期12例(10.8 %)、IV期13例(10.9 %)。所有病理标本均未发现肿瘤或结核。骨折时间与骨组织形态学改变呈显著正相关,镜下表现为骨折区域的修复变化:从早期血肿和炎性浸润到肉芽期织和纤维组织的增生,进一步软骨成骨、钙盐沉积,最终形成新的编织骨。骨组织形态学测量结果显示I期、II期FV/TV(%)显著增高(P<0.0001,r=0.4882),III期OS/BS(%)显著增高(P<0.0001,r= -0.5727),IV期WBV/TV(%)显著增高(P<0.0001,r= -0.5836)。结论 骨折时间是骨折愈合分期重要的预测因素,发病时间不同,其椎体内部的病理变化也不尽相同。
英文摘要:
      Objective To observe the bone pathologic characteristics of sub and acute osteoporotic vertebral compression fracture (OVCF)at different healing stages. Methods According to the time since fracture, 119 patients were divided into four stages: Stage I (0 to 15 days), Stage II (15 days to 30days), Stage III (30 days to 60days), Stage IV (60 days to 90days). Decalcified biopsy specimen was obtained from the cancellous bone core in the fractured vertebral body. The histomorphometry study were analyzed by light microscopy using grid analysis and defined using bone histomorphometry criteria. Results 119 biopsy specimens were obtained, 67 (56.3%) patients in Stage I, 28 (23.5%) in Stage II, 12 (10.8%) in Stage III and 1 (10.9%) in Stage IV. No tumor or tuberculosis was found in all pathological specimens. There was a significant positive correlation between fracture time and bone histomorphometry. Microscopically, the changes were observed: From early hematoma and inflammatory infiltration to granulation weave and fibrous tissue proliferation, further cartilage osteogenesis, calcium salt deposition, and eventually the formation of new woven bone. Bone histomorphometry showed that FV/TV(%) in stage I and II increased significantly (P<0.0001,r=0.4882), OS/BS(%) in stage III increased significantly (P<0.0001,r= -0.5727), and WBV/TV(%) in stage IV increased significantly (P<0.0001,r= -0.5836). Conclusion The fracture time is an important predictor of healing stage. The pathological changes inside the vertebral body were also different with the onset time.
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