Institute for Science and Technology in Medicine, Keele University, and Department of Pathology, University Hospital of North Staffordshire, Thornburrow Drive, Hartshill, Stoke-on-Trent ST4 7QB, UK.
Phys Med Biol. 2010 Jul 7;55(13):3777-87. doi: 10.1088/0031-9155/55/13/014. Epub 2010 Jun 15.
The objective of this study was to develop a method based on polarization-sensitive optical coherent tomography (PSOCT) for the imaging and quantification of degenerative changes associated with Achilles tendon rupture. Ex vivo PSOCT examinations were performed in 24 patients. The study involved samples from 14 ruptured Achilles tendons, 4 tendinopathic Achilles tendons and 6 patellar tendons (collected during total knee replacement) as non-ruptured controls. The samples were imaged in both intensity and phase retardation modes within 24 h after surgery, and birefringence was quantified. The samples were fixed and processed for histology immediately after imaging. Slides were assessed twice in a blind manner to provide a semi-quantitative histological score of degeneration. In-depth micro structural imaging was demonstrated. Collagen disorganization and high cellularity were observable by PSOCT as the main markers associated with pathological features. Quantitative assessment of birefringence and penetration depth found significant differences between non-ruptured and ruptured tendons. Microstructure abnormalities were observed in the microstructure of two out of four tendinopathic samples. PSOCT has the potential to explore in situ and in-depth pathological change associated with Achilles tendon rupture, and could help to delineate abnormalities in tendinopathic samples in vivo.
本研究旨在开发一种基于偏振敏感光相干断层扫描(PS-OCT)的方法,用于成像和定量分析与跟腱断裂相关的退行性变化。对 24 例患者进行了离体 PSOCT 检查。研究涉及 14 例跟腱断裂、4 例腱病跟腱和 6 例髌腱(在全膝关节置换期间收集)作为非断裂对照的样本。在手术后 24 小时内,以强度和相位延迟模式对样本进行成像,并对双折射进行定量。成像后立即对样本进行固定和处理,以便进行组织学评估。采用双盲法对幻灯片进行了两次评估,以提供退行性变的半定量组织学评分。展示了深入的微观结构成像。PS-OCT 可以观察到胶原组织紊乱和高细胞密度,这是与病理特征相关的主要标志物。双折射和穿透深度的定量评估发现非断裂和断裂肌腱之间存在显著差异。在 4 例腱病样本中的 2 例中观察到微观结构异常。PS-OCT 具有探索与跟腱断裂相关的原位和深度病理变化的潜力,并有助于在体内描绘腱病样本的异常。