|
“ 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 |