1 / 62

Computational Medical Imaging Analysis Chapter 7: Biomedical Applications

Computational Medical Imaging Analysis Chapter 7: Biomedical Applications. Jun Zhang Laboratory for Computational Medical Imaging & Data Analysis Department of Computer Science University of Kentucky Lexington, KY 40506. 7.1a: Neuronal Microanatomy and Function.

nigel
Download Presentation

Computational Medical Imaging Analysis Chapter 7: Biomedical Applications

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Computational Medical Imaging Analysis Chapter 7: Biomedical Applications Jun Zhang Laboratory for Computational Medical Imaging & Data Analysis Department of Computer Science University of Kentucky Lexington, KY 40506 Chapter 7: CS689

  2. 7.1a: Neuronal Microanatomy and Function • Rapid growth of 3D visualization of microscopic structures happens with the advent of • Light and electron microscopy (classical) • Confocal microscopy • Atomic force microscopy • Tunneling microscopy Chapter 7: CS689

  3. 7.1b: Light and Electron Microscopy • Light microscopy images digitized directly from the microscope can provide a 3D volume image by incrementally adjusting the focal plane • It is usually followed by image processing to deconvolve the image to remove blurred, out-of-focus structures • Electron microscopy can generate multiple planes by controlling the depth of focus • Further processing is necessary for selective focal plane reconstruction Chapter 7: CS689

  4. 7.1b*: Light Microscopes Chapter 7: CS689

  5. 7.1b**: Electron Microscope ($69,000) Chapter 7: CS689

  6. 7.1c: Confocal Microscopy • Confocal microscopy uses incoherent light or laser with precise optical control to selectively image specific parallel sections within the microscopic structure • Multiple image planes can be selected, providing direct volume image acquisition without the need of signal from structures outside of the plane of interest • These images are often acquired using specific fluorescent dyes to selectively image a particular component of the structure under study Chapter 7: CS689

  7. 7.1c*: Confocal Microscope Chapter 7: CS689

  8. 7.1c**: Confocal Microscopy Images Chapter 7: CS689

  9. 7.1c**: Confocal Microscopy Images Chapter 7: CS689

  10. 7.1d: Neuron Visualization • The morphology and function of neurons from selected ganglia in the mammalian peripheral autonomic nervous system can be visualized • Information about a neuron’s shape and dimensions is needed to integrate and localize multiple synaptic inputs • The number and location of selective neurotransmitter receptor sites provides valuable information about the potential response of a neuron to a specific transmitter • Such visualization applications are termed as “spatial physiology” in which the function of microstructures are studies Chapter 7: CS689

  11. 7.1d*: Neuron Illustration Chapter 7: CS689

  12. 7.1d*: Single Neuron Chapter 7: CS689

  13. 7.1f: Imaging Neuron Architecture • Visualization of the architectural relationships between neurons is less well advanced • Nerve plexes, where millions of sensory nerve cells are packed into a few cubic millimeters of tissue, offer an opportunity to image a tractable number of cells in situ • This difficulty underscores the need for computer-assisted techniques to reconstruct neuronal architectures in vivo • They may not be visible directly from the images, but they can be visualized with assisting techniques Chapter 7: CS689

  14. 7.1f*: Rat Neuron Chapter 7: CS689

  15. 7.2a: Corneal Cell Analysis • The density and arrangement of corneal cells is an indicator of the general health of the cornea • These factors are routinely evaluated to determine suitability for transplant • The corneal confocal microscope is a reflected-light scanning aperture microscope fitted for direct contact with a living human cornea • The image is a 3D tomographic optical image of the cornea • Algorithms are developed for automated measurement of local keratocyte nuclear density in the cornea Chapter 7: CS689

  16. 7.2b: Human Cornea Chapter 7: CS689

  17. 7.2c: Local Keratocyte Density • The sectional images represent a section about 15 microns thick and at 1 micron intervals through the entire depth of the cornea • Both global and local automated density counts in rabbit corneas correlate well to those obtained from conventional histologic evaluation of cornea tissue • A decrease in keratocyte density toward the posterior of the cornea was found Chapter 7: CS689

  18. 7.2d: Keratocyte Density Images Left: Corneal confocal image. Right: Nuclei counting Chapter 7: CS689

  19. 7.2e: In Vivo Study of Cornea Density In vivo confocal microscopy images show the presence of densely packed ovoid or elliptical cell bodies, decreasing after birth for a neonate Chapter 7: CS689

  20. 7.2f: Cornea Density of Neonate Laser scanning micrographs of neonatal corneas show decreasing cell density after birth, confirming the in vivo confocal microscopy images Chapter 7: CS689

  21. 7.3a: Trabecular Tissue Analysis in Glaucoma • The trabecular tissue of the eye is a ring of spongy, fluid-filled tissue situated at the junction of cornea, iris, and sclera • This tissue lies in the only outflow path for aqueous humor, it has long been implicated in the eye disease glaucoma • The architecture of the trabecular tissue is so complex that most studies have focused on the architecture of the connected fluid space Chapter 7: CS689

  22. 7.3a*: Trabecular Tissue Image Chapter 7: CS689

  23. 7.3b: Connected Fluid Space Analysis • The fluid space is generally continuous from the anterior chamber through the trabecular tissue into Schlemm’s canal • Morphometric analysis (in which small chambers were successively closed) revealed that the interconnection is maintained by very small chambers • There are a large number of these narrowings, and they occur at all regions of the tissue Chapter 7: CS689

  24. 7.3c: Connected Fluid Space in Human Trabecular Tissue Before (left) and after (right) morphological opening Chapter 7: CS689

  25. 7.4a: Prostate Microvessels • It is common practice to surgically remove cancerous prostates, even though subsequent pathological examination of excised tissues suggest that some surgeries could have been avoided • There is a great need for improved non-invasive preoperative techniques that can more accurately measure tumor volume and extent • The measures of prostate tumor size and microvessel density are useful indicators of the metastatic potential of tumor Chapter 7: CS689

  26. 7.4a*: Prostate Cancer Chapter 7: CS689

  27. 7.4b: 3D Visualization of Microvessels • 3D image analyses show that the ratio of gland volume to vessel length exhibits a twofold increase between benign and malignant tumors • The normal tissue shows a characteristic circumferential pattern of the microvessels relative to the glandular tissue • In region with adenocarcinoma, the pattern of microvessels is tortuous and radically diffused throughout the glandular volume Chapter 7: CS689

  28. 7.4b**: Tumor & Neovasculature Chapter 7: CS689

  29. 7.4b*: Frog Microvessel Chapter 7: CS689

  30. 7.4c: Measurements of Microvessels • Neovasculature exhibits a statistically significantly larger standard deviation of curvature than the normal vessels • These measurements can be done with the images • Volume of tissue required for the histologic analysis is similar to that obtained via needle biospy • 3D image with biospy sample provides a marker for presurgical stage and outcome, improve patient population stratification and eliminate unnecessary surgeries Chapter 7: CS689

  31. 7.4c*: Stages of Prostate Cancer Chapter 7: CS689

  32. 7.5a: Prostate Surgery Planning • Radical prostatectomy is the most commonly performed surgical procedure • The procedure has significant morbidity • Minimizing these negative affects needs a careful balance between completely removal of all cancerous prostate tissue and sparing neural and vascular structures • Routine surgical rehearsal using patient specific data could have significant effect on procedural success Chapter 7: CS689

  33. 7.5b: Prostate Cancer Surgery Chapter 7: CS689

  34. 7.5c: Presurgical Rehearsal • Presurgical MR volume images of patients scanned with a rectal coil can be segmented to identify and locate the prostate, bladder, and other tissues • The segmented images can be constructed into faithful patient-specific models and reviewed by surgeons interactively before the surgery • The approach, margins, and critical tradeoffs can be evaluated and determined upon seeing the pathology localized relative to normal anatomy • Rendered views of patient-specific models of prostate cancer can be used to accurately assess the tumor size and location relative to sensitive structures Chapter 7: CS689

  35. 7.5d: Prostate Surgical Planning Chapter 7: CS689

  36. 7.6a: Craniofacial Surgery Planning and Evaluation • Craniofacial surgery (CFS) involves surgery of the facial and cranial skeleton and soft tissues • Preoperative information is most often acquired using X-ray CT scanning for the bony structures, with MRI used for imaging the soft internal tissues • 3D visualization facilitates accurate measurement of structures of interest, allowing precise design of surgical procedures • It also minimizes the duration of surgery, reducing the risk of postoperative complication and cost Chapter 7: CS689

  37. 7.6b: Craniofacial Surgery (I) Chapter 7: CS689

  38. 7.6c: Craniofacial Surgery (II) Chapter 7: CS689

  39. 7.6d: Craniofacial Surgery Planning Chapter 7: CS689

  40. 7.6e: Craniofacial Reconstruction (I) Chapter 7: CS689

  41. 7.6f: Craniofacial Reconstruction (II) Chapter 7: CS689

  42. 7.7a: Neurosurgery Planning • Neurosurgery needs extended knowledge and understanding of intricate relationships between normal anatomy and pathology • Multimodality scans are coregistered to help neurosurgeon understand anatomy of interest • Specific anatomical objects may be identified and segmented, creating object maps within the digital volumetric dataset • The diagnostic information is used to determine the margins of pathology, to avoid critical structures, e.g., cerebral vasculature and eloquent cortical tissue Chapter 7: CS689

  43. 7.7a*: Virtual Surgery Planning Chapter 7: CS689

  44. 7.7b: Neurosurgery Planning in Epilepsy Chapter 7: CS689

  45. 7.7c: Neurosurgery Planning in Tumor Resection Chapter 7: CS689

  46. 7.7d: Neurosurgery (I) Chapter 7: CS689

  47. 7.7e: Neurosurgery (II) Chapter 7: CS689

  48. 7.7f: Neurosurgery (III) Chapter 7: CS689

  49. 7.7g: Intraoperative Guidance • Interactive computation of line-of-sight oblique planar images for planning neurosurgical approach to large tumor • Neurosurgeon will have direct visualization of image planes along the path of surgical approach • T1-weighted MRI prior to contrast enhancement (2nd row), T1-wieghted MRI with gadolinium to define tumor size (3rd row), MR angiogram to localize position of important vessels (4th row) Chapter 7: CS689

  50. 7.7g*: Neurosurgery (IV) Chapter 7: CS689

More Related