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Investigation of optical coherence microelastography as a method to visualize cancers in human breast tissue

机译:研究光学相干微弹性成像作为一种可视化人乳腺组织癌症的方法

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摘要

An accurate intraoperative identification of malignant tissue is a challenge in the surgical management of breast cancer. Imaging techniques that help address this challenge could contribute to more complete and accurate tumor excision, and thereby help reduce the current high reexcision rates without resorting to the removal of excess healthy tissue. Optical coherence microelastography (OCME) is a three-dimensional, high-resolution imaging technique that is sensitive to microscale variations of the mechanical properties of tissue. As the tumor modifies the mechanical properties of breast tissue, OCME has the potential to identify, on the microscale, involved regions of fresh, unstained tissue. OCME is based on the use of optical coherence tomography (OCT) to measure tissue deformation in response to applied mechanical compression. In this feasibility study on 58 ex vivo samples from patients undergoing mastectomy or wide local excision, we demonstrate the performance of OCME as a means to visualize tissue microarchitecture in benign and malignant human breast tissues. Through a comparison with corresponding histology and OCT images, OCME is shown to enable ready visualization of features such as ducts, lobules, microcysts, blood vessels, and arterioles and to identify invasive tumor through distinctive patterns in OCME images, often with enhanced contrast compared with OCT. These results lay the foundation for future intraoperative studies. Cancer Res; 75(16); 3236-45. ©2015 AACR.
机译:在乳腺癌的外科手术处理中,准确的术中恶性组织识别是一个挑战。有助于解决这一难题的成像技术可有助于更完整,更准确地切除肿瘤,从而有助于降低当前的高切除率,而无需诉诸于去除多余的健康组织。光学相干微弹性成像(OCME)是一种三维高分辨率成像技术,对组织的机械特性的微小变化敏感。由于肿瘤改变了乳腺组织的机械性能,OCME有潜力在微观上识别新鲜,未染色组织的受累区域。 OCME基于光学相干断层扫描(OCT)来测量响应于施加的机械压缩的组织变形。在对来自进行乳房切除术或广泛局部切除术的患者的58个离体样本的可行性研究中,我们证明了OCME的性能,可作为可视化良性和恶性人乳腺组织微结构的一种手段。通过与相应的组织学图像和OCT图像进行比较,显示OCME可以使血管,小叶,微囊肿,血管和小动脉等特征随时可视化,并通过OCME图像中的独特图案识别侵入性肿瘤,与10月。这些结果为将来的术中研究奠定了基础。癌症研究; 75(16); 3236-45。 ©2015 AACR。

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