“ Multislice CT has made 3D imaging a routine procedure and virtual endoscopy a clinical reality” |

| A 3-dimensional reconstruction (in colour) of the abdominal blood vessels. The spine and rib cage is also visible. The images were obtained from a multislice CT Scan | 
| This is a coronal plane reconstruction of the abdomen from CT scan images obtained in the transverse plane | 
| The picture on your left is a photo of a fleshy polyp obtained during conventional colonoscopy (using an endoscope) while that on the right is that obtained using virtual colonoscopy from images obtained from CT Scan. In a CT Scan, no scope needs to be inserted through your anus into the large bowel (the colon). From the images obtained, computerized software is used to obtain a virtual colonoscopy |
The increasing computer power in cross-sectional imaging has facilitated the acquisition of 3-dimensional data, permitting high resolution volumetric acquisition of images, thus facilitating diagnosis. Multi-row detector Computed Tomography and 3D Magnetic Resonance Imaging (MRI) have also made virtual endoscopy an increasingly accepted clinical imaging technique. This technique is presently being applied to practically every anatomic channel: colon, esophagus, stomach, small bowel, bronchial tree, blood vessels, urinary tract (including the bladder) etc. Virtual endoscopy promises to reduce the number of invasive procedures and limit conventional, invasive endoscopic procedures to targeted biopsy if the virtual studies disclose abnormalities. Fusion of images generated from different imaging modalities, such as MR, CT and PET is showing that advantages of two techniques can be maximized. Several large equipment manufacturers are already marketing PET-CT scanners for clinical use. The advantages of PET's ability to detect malignant lymph nodes are thus combined with the superior spatial resolution of CT. Several companies are presently designing combined MR-PET instruments which will have important applications particularly in the brain. Fusion of MR and CT is currently used in radiation therapy planning. 
| This shows a suite with both PET and CT equipment housed within and viewed from the console room.. |
Proton spectroscopic MR imaging has presently become clinical in the study of brain tumors and prostate carcinoma. A grid is superimposed on the MR image and the voxels can display in color the ratio of choline and NAA for the study of brain tumors. This is particularly valuable in the differentiation of tumor recurrence from necrosis following therapy. For prostate cancer the use of different three dimensional spectroscopic imaging displays of choline and citrate resulted in improved detection, diagnosis of extra-capsular spread, assessment of tumor aggressiveness and evaluation of treatment. In the future, as MRSI (Magnetic Resonance Spectroscopic Imaging) expands its role, other normal function chemical spectroscopic markers will be identified in addition to NAA for the brain and citrate for the prostate. Other MR spectroscopic markers for cancer even more specific than increased choline levels, will be d proteins. This mechanism needs much more research. It does change the original concept that each disease is related to one mutated gene. These factors will need much more study and they do affect the future of medical imaging. also be identified. Extension of these successful MR spectroscopic techniques to breast cancer and brain development and identification of birth injury in neonates is underway in multiple centers. 
| Cross Sectional Brain Images obtained in functional MRI showing areas of activity (in red) when the person does the action of finger apposition |
Mapping of foci of specific brain activity with functional MRI by displaying images of metabolic activity data, as for instance for heat/pain sensation, motor, memory centers etc. is becoming the basis of functionally based medicine and will have an important future role in the study of mental diseases. The development of new imaging modalities like optical coherence tomography, adds new dimensions to medical imaging. It is expected that it will be possible in the future to identify early dysplastic, precancerous changes in many organs. Examples are changes in Barrett's esophagus as well as in the bronchial mucosa of heavy smokers. |
I. Feig S.A., Yafee MJ. Digital mammography, computer-aided diagnosis and tele-mammography. Radiol. Clin. North Am, 1995; 3:1205-1230 2. Moshage WE, Achenbach S, Seese B, Bachmann K, Kirchgeorg M. Coronary artery stenoses: three-dimensional imaging with electrocardiographically triggered, contrast agent-enhanced, electron-beam CT. Radiology, 1995, 196(3):707-714. 3. Collins FS, Patrinos A, Jordan E, et al. New goals for the U.S. human genome project: 1998-2003. Science, 1998; 282:682-689. 4. Johnson C.D.,Dachman AH. CT Colonography: The Next Colon Screening Examination? Radiology 2000;216: 331-341 5. Dachman, AH; Kuniyoshi, JK; Boyle, CM; Samara, Y; Hoffmann, KR; Rubin, DT; Hanan, I. CT colonography with three-dimensional problem solving for detection of colonic polyps. AJR. American Journal of Roentgenology, 1998; 171 (4):989-995. 6. Luboldt W, Bauerfeind P., Wildermuth S., Marincek B., Fried M., Debatin J.E Colonic Masses; Detection with MR Colonography Radiology 2000:216 383-388 7. Tang Y. Yamashita Y, Arakawa A, Namimoto T, Mitsuzaki K., Abe Y, Katahira K, Takahashi M: Pancreaticobiliary Ductal System: Value of Half-Fourier Rapid Acquisition with Relaxation Enhancement MR Cholangiopancreatography for Postoperative Evaluation Radiology 2000; 215:81-88 8. Lee CC,Jack CRJr, Riederer SJ. Use of functional magnetic resonance imaging. Neurosurg Clin N Am, 1996; 7(4):665-683. 9. Kurhanewicz J, Vigneron DB, Hricak H, Narayan P, Carroll P, Nelson SJ. Three-dimensional H-I MR spectroscopic imaging of the in situ human prostate with high (0.24-0.7 cm 3) spatial resolution. Radiology, 1996; 198(3):795-805. 10. Nelson SJ, Huhn S, Vigneron DB, et al Volume MRI and MRSI techniques for the quantitation of treatment response in brain tumors: presentation of a detailed case study. J Magn Reson Imaging, 1997; 7(6):1146-1152. 11. G. J. Tearney,Ph.D., M.E. Brezinski, M.D., Ph.D., J.F.Southern, M.D., B.E. Bouma Ph.D., S.A. Boppart M.S.E.E. and J.G. Fujimoto, Ph.D.; Optimal Biopsy in Human Gastrointestinal Tissue Using Optical Coherence Tomography. The American Journal of Gastroenterology 1997, 92: 1800-1804 12. Varmus H and Weinberg RA, Genes and the Biology of Cancer, 1993 Scientific American library, New York 13. Weissleder R and Mahmood U. Molecular Imaging, Radiology 2001,219:316-333 14. Lander ES et al. Initial sequencing and analysis of the human genome, Nature 2001 409: 814-823 15. Venter JC et al The sequence of the human genome, Science 2001 291: 1304-1351 16. Hillman B.J. and Neiman H.L Translating Molecular Imaging Research into Practice: summary of the Proceedings of the American College of Radiology Colloquium April 22-24, 2001, Radiology 2002 222: 19-24 >>> Back to General Health Information |