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Optical palpation for the visualization of tumor in human breast tissue.

Abstract
Accurate and effective removal of tumor in one operation is an important goal of breast-conserving surgery. However, it is not always achieved. Surgeons often utilize manual palpation to assess the surgical margin and/or the breast cavity. Manual palpation, however, is subjective and has relatively low resolution. Here, we investigate a tactile imaging technique, optical palpation, for the visualization of tumor. Optical palpation generates maps of the stress at the surface of tissue under static preload compression. Stress is evaluated by measuring the deformation of a contacting thin compliant layer with known mechanical properties using optical coherence tomography. In this study, optical palpation is performed on 34 freshly excised human breast specimens. Wide field-of-view (up to ~46 × 46 mm) stress images, optical palpograms, are presented from four representative specimens, demonstrating the capability of optical palpation to visualize tumor. Median stress reported for adipose tissue, 4 kPa, and benign dense tissue, 8 kPa, is significantly lower than for invasive tumor, 60 kPa. In addition, we demonstrate that optical palpation provides contrast consistent with a related optical technique, quantitative micro-elastography. This study demonstrates that optical palpation holds promise for visualization of tumor in breast-conserving surgery.
AuthorsWes M Allen, Philip Wijesinghe, Benjamin F Dessauvagie, Bruce Latham, Christobel M Saunders, Brendan F Kennedy
JournalJournal of biophotonics (J Biophotonics) Vol. 12 Issue 1 Pg. e201800180 (01 2019) ISSN: 1864-0648 [Electronic] Germany
PMID30054979 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Topics
  • Breast Neoplasms (diagnostic imaging, pathology, surgery)
  • Humans
  • Image Processing, Computer-Assisted
  • Mastectomy
  • Optical Imaging
  • Palpation (methods)
  • Tomography, Optical Coherence

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