Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_1185_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
15.09.2026
Размер:
17 Мб
Скачать
☆
90 M.G. Mutch, E.H. Birnbaum, and C.O. Menias
FIGURE 6-34. CT scan of SBO with evidence of ischemia.
information that can indicate concern for vascular compro­mise. Thickened, congested bowel with increased attenuation at the site of obstruction associated with engorgement of the mesenteric vasculature is concerning for strangulation (Figure 6-34). The mesentery may become hazy or the vasculature may be obliterated as the inflammation progresses and it becomes filled with fluid or even blood. Other findings of ischemia include lack of enhancement after IV contrast administration or the presence of ascites. The presence of pneumatosis and portal venous gas are the more ominous signs of intestinal ischemia. Finally, a spiral pattern of engorged mesenteric blood vessels may indicate an internal hernia or rotation of small intestine around fixed adhesions.
Postoperative Evaluation
CT has greatly impacted the postoperative evaluation of the surgical patient. It is typically used to evaluate a patient with abdominal pain, fevers, leukocytosis, or persistent ileus in the postoperative period. The yield of a CT scan is greatest when it is obtained 5 days or more after surgery. Before postopera­tive day five, it is difficult to differentiate normal postopera­tive intraperitoneal free air or fluid from air or fluid that represents a leak from a hollow viscus or infected fluid. It usually takes more than 5 days for an abscess to organize into a walled-off, contained collection. Once again, the findings of the CT scan must be interpreted in the context of the clinical condition of the patient. Therefore, the yield will be greatest when the scan can address a specific question.
Findings highly suggestive of an anastomotic leak include an inappropriate volume of free air or fluid in the abdomen. The presence of extraluminal oral contrast
FIGURE 6-35. CT scan of colorectal anastomotic leak.
confirms a perforation of a hollow viscus. The presence of localized fluid and air around an anastomosis are concerning for a leak but must be taken in context to the postoperative period and the condition of the patient. As mentioned above, water-soluble enemas are more sensitive than a CT with rec­tal contrast at detecting a colorectal anastomotic leak. However, a CT is often more easily and readily obtained. An abscess is defined as an organized fluid collection with or without air that has an enhancing rim (Figure 6-35). As mentioned above, CT is very good at distinguishing between an ileus and a mechanical bowel obstruction, which is an important distinction in the perioperative period.
Other Colitides
There are a handful of inflammatory processes that affect the colon that have not been addressed. The CT findings are very similar for all inflammatory processes of the colon. However, their clinical presentations are different, so combining the presenting signs and symptoms with the distribution of CT findings will usually lead to the correct diagnosis. This sec­tion will briefly address some these remaining processes.
Neutropenic enterocolitis or typhlitis typically occurs in patients who are neutropenic either from cytotoxic chemo­therapy or severe immunosuppression. The terminal ileum, cecum, and right colon are most frequently affected. CT is the study of choice for the diagnosis. Circumferential thickening of the terminal ileum, cecum, and variably the right colon are the common CT findings consistent with typhlitis (Figure 6-36). The bowel wall may become so thickened because of edema that a hypodense ring develops between the mucosa and musculature. Complications such as pneumatosis or per­foration can also be detected.
6. Diagnostic Evaluations—Radiology, Nuclear Scans, PET, CT Colography 91
FIGURE 6-36. CT scan of neutropenic enterocolitis.
Ischemic colitis is the most common vascular abnormality of the colon. Presenting symptoms include abdominal pain associated with bloody diarrhea. The age of the patient and onset of symptoms will help to differentiate between IBD, infectious colitis, and ischemic colitis. Endoscopy is the gold standard for diagnosing ischemic colitis. CT is much more readily available so it is often the first test ordered. The coli­tis may be segmental or diffuse, typically occurring in the watershed areas of the right colon, splenic flexure, and rec­tosigmoid. CT findings consist of thickened, edematous colon in these areas (Figure 6-37). The typical “thumbprinting” in the colonic mucosa can be seen on CT scan as well as plain films. There may be a halo sign of either low attenuation caused by edema or high attenuation caused by hemorrhage within the bowel wall. A pericolonic inflammatory response is often present as well. Thrombus within the colonic
FIGURE 6-37. CT scan of ischemic colitis.
FIGURE 6-38. CT scan of pseudomembranous colitis.
mesenteric vessels may also be seen. Finally, pneumatosis or portal venous gas may be present indicating bowel infarction.
Pseudomembranous colitis resulting from the toxins pro­duced by Clostridium difficile can cause profound inflamma- tion of the colon. Computed tomographic findings include nonspecific thickening and edema of the colon and peri­colonic inflammation. Generally, the edema and thickening of the colon is greater than that seen with infectious colitis or other inflammatory processes. The presence of pancolitis also tends to suggest pseudomembranous colitis versus other coli­tides (Figure 6-38). Once again, the CT results must be inter­preted in the clinical context of the patient.
Radionuclide Imaging
Radionuclide imaging studies base their imaging on physiol­ogy rather than anatomy, and have a wide spectrum of use in clinical medicine. Radiopharmaceuticals and gamma cameras are the mainstay of radionuclide imaging. The specific radionuclides are chosen based on either the biologic proper­ties of the element (i.e., iodine has an affinity for thyroid tis­sue) or the physical and chemical properties that allow linkage to appropriate compounds. These radiolabeled com­pounds are given to a patient to localize within a specific organ system (such as the thyroid) or identify the sight of an ongoing physiologic process (as in GI bleeding). The quality of a scan depends on how well the agent targets the organ or the physiologic process. A gamma camera is used to acquire images once the agent is given to the patient. Gamma and X-ray photons are absorbed and converted into flashes of
38
light.
The location and intensity of these scintillation events are determined and recorded. Spot images are generally taken in 10-minute intervals and the completed image reflects the
92 M.G. Mutch, E.H. Birnbaum, and C.O. Menias
distribution of scintillation events (counts) detected during the acquisition phase. Image quality improves as the number of counts increases.
Radionuclide imaging studies are widely used in the diag­nosis of lower GI bleeding. The principle is that the intra­vascular tracer will be extravasated into the bowel lumen during active bleeding. Concentration of the tracer on the acquired images allows identification of the bleeding sight. Technetium
99m
Tc is the radionuclide used in bleeding scans. This radiopharmaceutical can label colloid or red blood cells for scanning purposes. Radiolabeled colloid is readily avail­able, but is metabolized rapidly. Red blood cells take longer to label but clearance of the tagged cells is prolonged and the tracer can remain active up to 24 hours after injection. Most centers prefer to use tagged red blood cells because lower GI bleeds are characteristically intermittent and the opportunity to identify the active bleeding sight lasts only a few minutes with labeled colloid. The preparation for a tagged red blood cell scan requires an aliquot of the patient’s blood to be labeled with
99m
Tc. Once labeled,
99m
Tc red blood cells are injected back into the patient and the patient is imaged with 10-minute acquisition intervals for approximately 60–120 minutes. Focal areas of increased activity identified within the lumen of the bowel indicate that active bleeding occurred dur­ing this acquisition period (Figure 6-39). A positive scan may localize the region of bowel that contains the bleeding site, but may not accurately localize the specific site, if the bleed­ing is slow or intermittent. The labeled red blood cells remain in circulation as long as the cells are viable and the limiting factor to imaging is the half-life of the
99m
Tc. If no bleeding occurs during the initial acquisition phase, then delayed views can be obtained up to 24 hours later to determine whether active bleeding has occurred. Bleeding scans have greater prognostic value than diagnostic value when the tracer is only seen on delayed images.
39,40
The location of activity seen on delayed images does not reflect the exact bleeding sight but does indicate that active bleeding occurred during this obser­vation period. The accuracy for localizing the actual bleeding site increases if the extravasation of tracer is identified within the first 15–30 minutes.
36
The longer it takes the tracer to
accumulate, the less likely the bleeding site will be accurately
identified by angiography. Backwash and washout of blood caused by peristalsis account for some of this inaccuracy.
Bleeding scans are more sensitive than angiograms in the detection of lower GI bleeding. The required rates of bleeding for detection are lower for bleeding scans (0.1–0.2 mL per
37,41
minute) than for angiograms (0.5 mL per minute).
The early (within 3 minutes) detection of intraluminal tracer indi­cates a high likelihood of successful arteriographic localiza­tion of the bleeding site. For this reason, some interventional radiologists require a positive scan before performing angiog­raphy. The addition of early colonoscopy to the diagnostic algorithm requires a bowel preparation. Cathartics will remove any intraluminal tracer making delayed images worthless. If the patient is hemodynamically unstable and rap­idly bleeding, some centers may prefer to go directly to arte­riograms because the time involved in pretest preparation for tagged red blood scans may be too lengthy.
A Meckel’s scan, although not used as often as the tagged red blood scan, can be useful in the evaluation of patients with occult bleeding with no identifiable colonic source. These scans are generally limited to the evaluation of children and young adults who have complaints of abdominal pain and intestinal bleeding. The abnormal bleeding from a Meckel’s diverticulum is caused by the aberrant gastric mucosa that lines the diverticulum. by mucous secreting cells in gastric mucosa. scans are performed with
99
Tc pertechnetate is actively extracted
99m
Tc per pertechnetate as a radio-
42,43
Meckel’s
label for the detection of ectopic gastric mucosa. Imaging is usually done for approximately 30–60 minutes after injection of the tracer. All views should be obtained early because the tracer is extracted into the stomach and then into lumen of the GI tract. Rapid transit of the tracer through the GI tract will obscure extravasation on later images.
A focus of increased radioactivity outside of the stomach indicates ectopic gastric mucosa (Figure 6-40). Typically, the collection of activity is identified in the right lower quadrant within 10–20 minutes. The sensitivity of the Meckel’s scan is 85% and the specificity is 95%.
43
Arteriography
FIGURE 6-39. pool activity within the ascending colon in this patient with bleeding after a recent polypectomy.
99m
Tc-tagged red blood cell study shows early blood
Arteriography is an invasive procedure performed by spe­cialty trained physicians and is used in the diagnosis and treatment of a variety of colorectal diseases. The arteriogram is performed through a percutaneous approach under sterile conditions. The femoral artery is a preferred puncture sight although axillary and brachial arteries may be used. A guidewire is introduced through the needle and a catheter is introduced over the guidewire. Various catheters and guide wires allow the interventional radiologist to access the vessels in question.
Arteriography is an invasive procedure with an overall mor­tality of one in 40,000.
44
Complications from the performance
of the procedure and manipulation of the wires and catheters
6. Diagnostic Evaluations—Radiology, Nuclear Scans, PET, CT Colography 93
FIGURE 6-40. focus of increased uptake in the right lower quadrant, with approxi­mately the same intensity as the stomach indicating gastric mucosa is present within this Meckel’s diverticulum.
99m
Tc-pertechnetate scan (Meckel’s) shows a discrete
are more common than reactions to the contrast itself.45The most common complications are related to hematomas or pseudoaneurysms at the puncture sight, dissection or embolization secondary to catheter manipulation. Contrast reactions and contrast toxicity (renal failure) occur in <1% of studies done. Experience and technique can minimize many of the complications. Hydration and IV mannitol can reduce the nephrotoxicity. If the patient has allergies to iodine or has had a prior contrast reaction, premedication with methyl pred­nisolone is done 12 and 2 hours before arteriography.
The arteriogram is a useful diagnostic and therapeutic modality in the treatment of active lower GI bleeding. If a radionuclide scan is performed and localizes the site of bleed­ing, a selective angiogram can then be performed. For bleeding localized to the left colon on tagged RBC study, the inferior mesenteric artery is selected first. The superior mesenteric artery is selected first for those bleeds that occur in the right colon. If the bleeding site is not identified after injection of both the superior and inferior mesenteric arteries, a celiac run is performed looking for an upper intestinal bleeding source. Active bleeding can be diagnosed by the accumulation of con­trast in the arterial phase that persists through the venous phase (Figure 6-41). Bleeding needs to occur at a higher rate for a positive angiogram (0.5 mL per minute) than for nuclear imag­ing (0.1–0.2 mL per minute). Because lower GI bleeding can be intermittent, the bleeding site is sometimes not identified at the time of the angiogram.
Diverticulosis and vascular ectasias are presumed to be the leading cause of lower GI bleeding in most patients.
FIGURE 6-41. Mesenteric angiogram shows pooling of contrast in the sigmoid colon in this patient with surgically proven diverticular bleeding.
Diverticular bleeds appear as a blush of contrast contained within a diverticulum. Vascular ectasias often occur in the right colon and appear as small vascular clusters, a blush in the wall of the colon and early opacification of a draining
46
vein.
Arteriovenous malformations are developmental in origin and are often seen in the small bowel. They appear as tortuous, dilated arteries and early prominent veins. Capillary telangiectasias (common in Osler Weber Rendu syndrome) appear as multiple, tiny areas of blush and no arteriovenous shunting. Postpolypectomy bleeding has been diagnosed and treated with angiography. A rapid blush of dye occurs at the site of bleeding and often stops with direct infusion of vaso­pressin or embolization (Figure 6-42).
Acute mesenteric ischemia is one of the most common intes­tinal disease processes for which arteriography is used for diag­nosis and treatment. Acute mesenteric ischemia can be either nonocclusive or occlusive. Nonocclusive mesenteric ischemia arises from a “low flow” state typically secondary to reduction in mesenteric blood flow from cardiac failure or hypotensive shock. This diagnosis can frequently be made with clinical symptoms and computer tomography images. The typical early angiographic images show diffuse vasoconstriction of mesen­teric arterial branches and decreased parenchymal vascularity (Figure 6-43). In the late stage there is increased accumulation of contrast in the bowel wall. Treatment includes volume resus­citation and cardiac support. The diagnostic percutaneous catheter can be used to treat the mesenteric phase of constriction with IV glucagon or intraarterial infusion of the papaverine in an intensive care unit setting.
Occlusive acute mesenteric ischemia is a medical emer­gency, thus early diagnosis and treatment may prevent bowel
94 M.G. Mutch, E.H. Birnbaum, and C.O. Menias
FIGURE 6-43. Mesenteric angiogram shows vasoconstriction and pruning of the superior mesenteric artery and its branches in this patient who presented with mesenteric ischemia secondary to severe hypotension.
FIGURE 6-42. Mesenteric angiogram shows extravasation of contrast A indicating an acute bleed that was successfully treated after infu­sion of pitressin B.
necrosis and perforation. These patients typically have severe abdominal pain with nonspecific physical findings.
47
An arteriogram is the most useful diagnostic examination for patients in whom one has a high clinical suspicion of acute occlusive mesenteric ischemia.
48
A catheter is inserted into the aorta and an aortogram is obtained. The celiac and supe­rior mesenteric arteries are catheterized and injected with contrast in order to identify the level of occlusion and docu­ment collateral circulation. A superior mesenteric artery embolus typically lodges just proximal or distal to the take off of the middle colic artery and is seen as a meniscus at the site of occlusion and blockage of contrast (Figure 6-44). Atherosclerotic occlusion will often involve the origin of the superior mesenteric artery seen as stenosis or plaque with a trickle of glow beyond (Figure 6-45). Collaterals will develop from the inferior mesenteric artery through the mar­ginal artery. If the inferior mesenteric artery is occluded or absent, the collaterals will develop from the middle or infe­rior hemorrhoidal arterial branches of the internal iliac
48,49
artery.
CT Colonography
CT colonography is rapidly developing as a noninvasive total colonic examination for the detection of colon polyps and can­cers. This technique uses volumetric data acquired by helical CT scanners and workstations which use two- and three­dimensional images to evaluate data. Since 1994, there have been technical improvements in the CT hardware and software allowing better visualization and discrimination of the recon­stituted images. The three-dimensional endoluminal imaging is better at evaluation of surface morphology and discriminat­ing between polyps and haustral folds (Figure 6-46).
50
The
6. Diagnostic Evaluations—Radiology, Nuclear Scans, PET, CT Colography 95
FIGURE 6-46. Three-dimensional image confirms the presence of the polyp in Figure 6-45.
FIGURE 6-44. Mesenteric angiogram shows a large filling defect within the proximal superior mesenteric artery consistent with an embolism in this patient with ischemic bowel.
FIGURE 6-45. Axial two-dimensional image from a CT colon study shows a well-defined 6-mm polyp in the sigmoid colon.
two-dimensional images help in the correlation of images seen on the three-dimensional fly-through.
Image processing and interpretation has improved with newer software and an experienced radiologist can generally complete the examination in <15 minutes.
Although the colon is evaluated in a noninvasive way, a bowel preparation is still required the day before the exam­ination to eliminate formed fecal matter. Air insufflation is done via a small tube placed within the rectum to distend the bowel and to minimize folds within the colonic wall. Insufflation with a handheld bulb, or with a CO
insufflator is
2
performed. A CT tomogram is obtained to confirm adequate insufflation in both the prone and supine positions and further air is insufflated as needed. Unlike colonoscopy, IV sedation is not required. Patient satisfaction after colonoscopy and CT colonography are similar because bowel preparation is needed for both tests.
51
Rapid scanning can be done in a single breath hold. Volumetric data are acquired twice, once with the patient prone and once with the patient supine. The change in position allows any fluid within the bowel lumen to shift, revealing abnormalities within the contralateral wall. Most tests can be completed in <15 minutes. Once the images are acquired, a trained radiologist reviews them at the workstation and the images are recreated in such a way as to give an endoluminal view of the colon similar to that seen on colonoscopy. Several studies have compared CT colonography to colonoscopy for high- and low-risk patients. The sensitivity of this technique per individual patient ranges from 75% to 100% and the speci­ficity ranges from 72% to 100%.
50–54
Both the sensitivity and
specificity are dependent on the polyp size. In randomized,
96 M.G. Mutch, E.H. Birnbaum, and C.O. Menias
55
of flat lesions.
Acquiring images after a change from the prone to the supine position can frequently unmask hidden polyps and tagging residual stool with subsequent digital sub­traction is being evaluated.
58
An added benefit of the tech­nique is the potential for the discovery of incidental extracolonic findings. The dose of radiation used for CT colonography is less than for conventional CT with the result that the scanned images are not the same. Nonetheless, the incidence of clinically important extracolonic findings is approximately 11%.
59
Whether CT colonography can be used for mass screening of average-risk patients has yet to be determined. Currently, most centers are using CT colonography for those patients who have had incomplete colonoscopies or who cannot undergo colonoscopy for medical reasons. Clinical trials are ongoing as educational efforts and technical improvements are made in an attempt to improve this potential screening technique.
Positron Emission Tomography
Whole body positron emission tomography (PET) was origi­nally developed as a research technique in the 1970s. The clinical use of this technique has evolved over the past several
FIGURE 6-47. Axial attenuation corrected PET image A and fusion PET CT image B show an area of intense FDG uptake in the right hepatic lobe consistent with hepatic metastatic disease in this patient with cecal adenocarcinoma.
controlled trials, the specificity is greater for polyps larger than 1 cm than for polyps larger than 5 mm.
53
The detection of small (< 5 mm) polyps is poor in most studies with sensitivi­ties as low as 11.5%.
54,55
The importance of these small lesions continues to be debated by the medical community. A recent nonrandomized multicenter blinded study comparing CT colonography with colonoscopy found that the sensitivity for CT colonography detecting polyps ≥6 mm was 39% and those ≥10 mm was 55%.
56
This study acknowledged that the accu­racy of CT colonography varied between centers and with the experience of the radiologists. Interobserver variability can be significant and is evidence of the steep learning curve.
57
The main limitation of CT colonography has been distin-
guishing polypoid tissue from fecal matter and the detection
decades. This technique uses [18F] 2-fluoro-2-deoxy­glucose (FDG) which is a radiopharmaceutical glucose ana­log to measure increased glucose uptake and metabolism in rapidly dividing cells. Malignant and other rapidly dividing cells that have a high metabolic rate will take up FDG for use as a glucose substrate. The first metabolite of FDG is FDG-6­phosphate which is not a substrate for glucosephosphate isomerase because of the configuration of FDG. FDG-6­phosphate has a low membrane permeability and thus the labeled substrate accumulates intracellularly.
60
The imaging technique of PET utilizes differences in uptake of FDG in malignant versus benign cells. The intracellular accumulation concentrates the radiopharmaceutical analog, which appears “bright” upon imaging (Figure 6-47).
The performance of a PET scan requires that the patient fast for 4–6 hours before the injection of FDG. A urinary catheter is placed to minimize the effect of the accumulation of tracer in the bladder. Emission scans are then performed with the patient motionless shifting the table between scans to alter the field of view. Older techniques required that a patient remain motionless for approximately 1–2 hours. Newer tech­niques have reduced the scan per bed position to approxi­mately 2 minutes. Scans are then enhanced through a segmentation calibration and the scattered events outside the body are removed. Attenuation in each area is altered depend­ing on tissue within the region.
61
FDG PET has been used to evaluate metastatic disease and to improve staging accuracy (Figure 6-48). This technique images the whole body and is more sensitive than CT for the detection of hepatic and extrahepatic colorectal cancer
D-
6. Diagnostic Evaluations—Radiology, Nuclear Scans, PET, CT Colography 97
current CT and MRI scans. FDG PET is extremely useful in this arena because a positive FDG PET scan in the setting of no inflammation would indicate a local recurrence of a rectal can­cer. Furthermore, detection of small extrapelvic metastases is more accurate using FDG PET than CT or MRI. Thus, the use of FDG PET for staging or recurrent cancers may help plan or avoid expensive and possibly more morbid surgical procedures.
False-positive and false-negative tests have been reported to occur in several distinct situations. FDG is not a tumor-specific substance and increased FDG activity is seen in the normal urinary and GI tracts. The cellular glucose metabolism is also increased in inflammation as the increased uptake of FDG can be seen in leukocytes and macrophages. Inflammatory processes such as diverticulitis and pneumonia can lead to false-positive readings thus making it imperative to correlate positive PET findings with the clinical picture and conven­tional radiologic evaluation.
67,68
Detection of metastatic disease is dependent on the size and degree of metabolic activity. Limited spatial resolution may lead to false-negative readings for small, <1-cm lesions. Adenocarcinomas with a high mucinous content may result in false-negative readings because of the low cellularity of these cancers. Sensitivity can be as low as 59% for mucinous carci-
70
nomas.
The combination of CT and FDG PET imaging has reduced some of the inaccuracies and makes the study more readily correlated anatomically.
The routine use of FDG PET for primary cancers is more problematic. Although the risks and radiation doses are low and the technique is noninvasive, the cost per scan is very high. Thus, for primary cancers in which the information would not alter the planned surgical procedure, it is probably not indicated. However, in patients that are poor surgical risk, the findings in FDG PET may help avoid or alter the surgical procedure and might change the goal from a curative to pal­liative intent. Current CMS (HCFA) recommendations for reimbursed PET imaging in colorectal cancer include
1) evaluation of patients with a question of recurrent disease as indicated by rising CEA, 2) evaluation of resectability, and
3) evaluation of patients with locally advanced disease to determine unresectability on the basis of metastasis when the operation is a large otherwise debilitating procedure.
MRI is a continually evolving field of radiology. The tech-
FIGURE 6-48. CT scan in a patient who had prior rectal resection for carcinoma shows soft tissue mass in the surgical bed of the perirec­tal fat A. Follow-up PET examination B shows intense FDG uptake within this soft tissue mass consistent with recurrence.
metastases and the detection of local recurrence. The reported sensitivities for PET detection of liver metastases range from 89% to 95% and for extrahepatic metastases 87% to 92%. The use of FDG PET versus CT or MRI is based on the prem­ise that functional differences in tumor appear before size changes. Postoperative changes, particularly for rectal cancers, are difficult to evaluate using standard modalities. The distinc­tion between tumor and scar is not easily defined with the
nique was developed in the early 1980s and currently there is a wide range of MRI systems in use. This technique relies on the difference in tissue contrast or signal intensity. High sig­nal intensity appears white on the image whereas low signal intensity is dark. T
1
and T2refer to specific tissue properties that describe the way protons behave after being excited by a radiofrequency pulse in a strong magnetic field.
62–66
cific parameters chosen to acquire an image on an MR mag­netic system determine whether an image is T weighted. T1refers to the longitudinal relaxation rate and T refers to the transverse relaxation rate. Structures containing water appear black on T
1
-rated images and structures con-
taining fluid (cysts or gallbladder) are white on T
71,72
The spe-
2
-weighted
1
or T
69
2
2
98 M.G. Mutch, E.H. Birnbaum, and C.O. Menias
images. Unlike CT scans, iodinated contrast is not used for the performance of these scans. The contrast agents that have been developed can be used in patients with renal insufficien­cies, and those with iodinated contrast allergic reaction. The risk from MRI is attributed to the interaction between the strong magnetic field and certain implantable devices such as cardiac pacemakers, cerebral aneurysms clips, and cochlear implants.
The use of MR for intraabdominal bowel anatomy is lim­ited because of the peristaltic action of the bowel wall and motion of the abdominal cavity caused by respirations. MRI has evolved to be better than CT for tissue characterization and evaluation of tissues planes within the pelvis. The layers of the bowel wall can be visualized easily for evaluation of rectal cancers. The muscularis propria is low signal intensity and the submucosa has higher signal intensity.
73,74
The accu­racy of MRI for preoperative staging for rectal carcinoma continues to be evaluated. Contrast enhancement improves the correlation with histologic stage.
75
Endorectal MRI is sim-
ilar to endoluminal ultrasound for determination of tumor
FIGURE 6-50. Endoanal MRI image demonstrates a nondisrupted (normal) signal of the internal and external sphincter.
depth and nodal staging although some studies have shown ultrasound to be more accurate in determining local inva-
76,77
sion. able preoperative staging difficult.
Overstaging and interobserver variation make reli-
75,78
MRI more accurately predicts the circumferential resection margin (Figure 6-49). Several parameters help distinguish pathologic tissues. After pelvic irradiation, the radiation edema or fibrosis can be dif­ferentiated from tumor on T appears low signal in the T
2
-weighted images. The fibrosis
2
images and enhances slowly. Recurrent tumors have a higher signal and enhance quickly during dynamic gadolinium-enhanced scanning.
80,81
Changes in postradiation normal tissue result in slow tissue enhance­ment with gadolinium.
80
The anal sphincter and pelvic anatomy have been imaged with MR using an internal coil (Figure 6-50). The internal sphincter has higher signal intensity than the external sphinc-
79
ter. Pelvic muscle morphology, sphincter injuries, and abscesses can be identified. Clinical experience with MR has not been as extensive as with endoluminal ultrasound but comparative studies have been favorable. MRI of the pub­orectalis is better than endorectal ultrasound and capable of showing atrophy.
82
It remains to be seen what the role of MR will be in the evaluation of fecal incontinence because of vari­ability of scanner capabilities among institutions and limited access to high-performance scanners.
FIGURE 6-49. Endorectal MRI examination shows an ulcerated plaque-like cancer arising from the mucosa and extending to the first muscular layer of the muscularis propria.
References
1. Flak B, Rowley VA. Acute abdomen: plain film utilization and analysis. Can Assoc Radiol J 1993;44:423–428.
2. Simeone JF, Novelline RA, Ferrucci JT, et al. Comparison of sonography and plain films in the evaluation of the acute abdomen. AJR Am J Roentgenol 1985;144(1):49–52.
3. Mirvis S, Young J, Keramati B, et al. Plain film evaluation of patients with abdominal pain: are three radiographs necessary? AJR Am J Roentgenol 1986;144:501–503.
4. Maglinte D, Heitkamp D, Howard T, et al. Current concepts in imaging of small bowel obstruction. Radiol Clin North Am 2003;41:263–283.
5. Miller G, Boman J, Shier I, et al. Etiology of small bowel obstruction. Am J Surg 2000;180:33–36.
6. Ogilvie H. Large intestine colic due to sympathetic deprivation. Br Med J 1948;2:671–673.
7. Sarr MG, Bulkey GB, Zuidena GD, et al. Preoperative recogni­tion of intestinal strangulation obstruction. Prospective evalua­tion of diagnostic capability. Am J Surg 1983;145:176–182.
8. Rigler LG. Spontaneous pneumoperitoneum: a roentgenologic sign found in the supine position. Radiology 1941:37:604–607.
6. Diagnostic Evaluations—Radiology, Nuclear Scans, PET, CT Colography 99
9. Miller RE, Nelson SW. The roentgenological demonstration of tiny amounts of free intraperitoneal gas: experimental and clini­cal studies. AJR Am J Roentgenol 1971;112:487–490.
10. Ly J. The Rigler sign. Radiology 2003;228:706–707.
11. Miller RE, Becker GJ, Slabaugh RA. Detection of pneumoperi­toneum: optimum body position and respiratory phase. AJR Am J Roentgenol 1980;135:487–490.
12. Levine MS, Scheiner JD, Rubesin SE, et al. Diagnosis of pneu­moperitoneum on supine abdominal radiographs. AJR Am J Roentgenol 1991;156:731–735.
13. Almer S, Bodemar G, Franzen L, et al. Plain X-ray films and air enema films reflect severe mucosal inflammation in acute ulcer­ative colitis. Digestion 1995;56:528–533.
14. Walsh JM, Terdiman JP. Colorectal cancer screening: clinical applications. JAMA 2003;289:1297–1302.
15. Fork ET, Ekberg O, Nilsson G, et al. Colon cleansing regimens. Gastrointest Radiol 1982;7:383–389.
16. Klabunde CN, Jones E, Brown ML, et al. Colorectal cancer screen­ing with double-contrast barium enema: a national survey of diag­nostic radiologists. AJR Am J Roentgenol 2002;179:1419–1427.
17. Winawer SJ, Stewart ET, Zauber AG, et al. A comparison of colonoscopy and double-contrast barium enema from surveil­lance after polypectomy. New Engl J Med 2000;342:1766–1772.
18. Kronborg O. Colon polyps and cancer. Endoscopy 2004;36:3–7.
19. Yamamoto M, Mine H, Kusumoto H, et al. Polyps with different grades of dysplasia and their distribution in the colorectum. Hepatogastroenterology 2004;51:121–123.
20. Levine MS, Rubesin SE, Laufer I, et al. Diagnosis of colorectal neoplasms at double-contrast barium enema examination. Radiology 2000;216:11–18.
21. McCarthy PA, Rubesin SE, Levine MS, et al. Colon cancer: mor­phology detected with barium enema versus histologic stage. Radiology 1995;197:683–687.
22. Hizawa K, Iida M, Kohrogi N, et al. Crohn’s disease: early recognition and progress of aphthous lesions. Radiology 1994; 190:451–454.
23. Najjar SF, Jamal MK, Savas JF, et al. The spectrum of colovesical fistula and diagnostic paradigm. Am J Surg 2004;188: 617–621.
24. Almer S, Bodemar G, Franzen L, et al. Use of air enema radiol­ogy to assess depth of ulceration during acute attacks of ulcera­tive colitis. Lancet 1996;347:1731–1735.
25. Giardiello FM, Bayless TM. Colorectal cancer and ulcerative colitis. Radiology 1996;199:28–30.
26. Nolan DJ, Traill ZC. The current role of barium examinations of the small intestine. Clin Radiol 1997;52:809–820.
27. Scott DJ, Guthrie JA, Arnold P, et al. Dual phase helical CT ver­sus portal venous phase CT for the detection of colorectal liver metastases: correlation with intra-operative sonography, surgical and pathological findings. Clin Radiol 2001;56:235–242.
28. Larimore T, Rhea J. Computed tomography evaluation of diver­ticulitis. J Intensive Care Med 2004;19:194–204.
29. Jarrett TW, Vaughan ED Jr. Accuracy of computerized tomogra­phy in the diagnosis of colovesical fistula secondary to divertic­ular disease. J Urol 1995;153:44–46.
30. Furukawa A, Yamasaki M, Takahashi M, et al. CT diagnosis of small bowel obstruction: scanning technique, interpretation and role in the diagnosis. Semin Ultrasound CT MR 2003;24:336–352.
31. ASCRS.
32. Maglinte DDT, Kelvin FM, O’Connor K, et al. Current status of small bowel radiology. Abdom Imaging 1996;21:247–257.
33. Shrake PD, Rex DK, Lappas JC, et al. Radiographic evaluation of suspected SBO. Am J Gastroenterol 1991;86:175–178.
34. Anthony T, Simmang C, Hyman N, et al. Practice parameters for the surveillance and follow-up of patients with colon and rectal cancer. Dis Colon Rectum 2004;47:807–817.
35. Bhattacharjya S, Bhattacharjya T, Bader S, et al. Prospective study of contrast-enhanced computed tomography, computed tomography during arterioportography, and magnetic resonance imaging for staging colorectal liver metastasis for liver resection. Br J Surg 2004;91:1361–1369.
36. Ng DA, Opelka FA, Beck DF, et al. Predictive value of tech­netium Tc 99-M-labeled red blood cell scintigraphy for positive angiogram in massive lower gastrointestinal bleeding. Dis Colon Rectum 1997;40:471–477.
37. Siddiqui AR, Schanwekcer DS, Wellman HN, et al. Comparison of tech-99-M sulfur colloid and in vitro labeled technetium-99M RBCs in the detection of GI bleeding. Clin Nucl Med 1985; 8:546.
38. Sorenson JA, Phelps ME. Physics in Nuclear Medicine. 2nd ed. Orlando: Grune & Stratton; 1987:298.
39. Winzelberg GG, McKusick KA, Froelich JW, et al. Detection of gastrointestinal bleeding with TC-99m labeled red blood cells. Semin Nucl Med 1982;12:139–146.
40. Jacobson AF, Cerqueira MD. Prognostic significance of late imaging results in technetium-99m-labeled blood cell gastroin­testinal bleeding studies with early negative images. J Nucl Med 1992;33:202–207.
41. Alavi A, Dann RW, Baum S, et al. Scintigraphic detection of acute GI bleeding. Radiology 1977;124:753.
42. Sfakianakis GN, Conway JJ. Detection of ectopia gastric mucosa in Meckel’s diverticulum and in other aberrations by scintigra­phy. I. Pathophysiology and 10 year clinical experience. J Nucl Med 1981;22:647–654.
43. Sfakianakis GN, Conway JJ. Detection of ectopia gastric mucosa in Meckel’s diverticulum and in other aberrations by scintigra­phy. II. Indications and methods—a 10-year experience. J Nucl Med 1981;22:732–738.
44. Witten DM, Hirsch FD, Hartman GW. Acute reaction to uro­graphic contrast medium: incidence, clinical characteristics and relationship to history of hypersensitivity states. AJR Am J Roentgenol 1973;119:832–840.
45. Hessel SJ, Adams DF, Abrams HL. Complications of angiogra­phy. Radiology 1981;138:273.
46. Baum S, Athanasoulis CA, Waltman AC, et al. Angiodysplasia of the right colon: a cause of gastrointestinal bleeding. AJR Am J Roentgenol 1977;129:789.
47. Tomchik FS, Wittenberg J, Ottinger LW. The roentgenographic spectrum of bowel infarction. Radiology 1970;96:249.
48. Flickinger EG, Johnsrude IS, Ogburn NL, Weaver MD, Pories WJ. Local streptokinase infusion for SMA thromboembolism. AJR Am J Roentgenol 1983;140:771–772.
49. Odurny A, Sniderman KW, Colapinto RF. Intestinal angina: per­cutaneous transluminal angioplasty of the celiac and SMA arter­ies. Radiology 1988;167:59.
50. Yee J, Akerkar GA, Hung RK, et al. Colorectal neoplasia: per­formance characteristics of CT colonography for detection in 300 patients. Radiology 2001;219:685.
51. Ristvedt SL, McFarland EG, Weinstock LB. Patient preferences for CT colonography, conventional colonoscopy, and bowel preparation. Am J Gastroenterol 2003;98:578.