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CHAPTER 8 The Gastrointestinal Tract 269

Classic Features

Gut Wall Thickening

Gut wall thickening is the most frequently observed abnormality

in patients with Crohn disease and varies in proportion to disease

severity. Its identiication comprises the basis for initial disease

detection, for detection of recurrence, 24 and for determining the

extent of disease. In a meta-analysis on the accuracy of sonography

in detecting Crohn disease, Fraquelli et al. 25 showed sensitivity

and speciicity of 88% and 93%, respectively, when a bowel wall

thickness threshold greater than 3 mm was used, and 75% and

97% with a threshold greater than 4 mm.

Gut wall thickening in Crohn disease is most frequently

concentric and may be marked. 26,27 Wall echogenicity varies

depending on the degree of inlammatory iniltration and ibrosis.

Stratiication with retention of the gut layers is typical (Fig. 8.13A

and B; also see Fig. 8.2, Videos 8.2 and 8.3). A target or pseudokidney

appearance is possible in acute disease or long-standing

ibrotic or subacute inlammatory disease as the gut wall layering

is progressively lost (Fig. 8.13C and D). Long-standing and oten

burnt-out disease may also show wall thickening with fat deposition

in the submucosa, which appears as increased echogenicity

of this layer (Fig. 8.13E and F). Actively involved gut typically

appears rigid and ixed, with decreased or absent peristalsis (Video

8.4). Involvement of the serosal border of the bowel may result

in spiculation of the border of the bowel (Fig. 8.14). Skip areas

are frequent. Involved segments vary in length from a few millimeters

to many centimeters. Bowel wall thickening may be

caused by acute inlammatory change or related to chronic ibrosis

and smooth muscle hypertrophy.

Inlammatory Fat

Mesenteric edema and inlammation of the mesenteric fat are

also characteristic of Crohn disease, producing a mass in the

mesentery adjacent to the diseased gut that may creep over the

border of the abnormal gut or completely engulf it, the so-called

creeping fat. Fat creeping onto the margins of the involved gut

creates a uniform echogenic halo around the mesenteric border

of the gut, with a thyroidlike appearance in cross section (Fig.

8.15). It may become more heterogeneous and even hypoechoic

in long-standing disease. Creeping fat is the most common cause

of gut loop separation seen on GI contrast studies. 21 It is also

the most striking and detectable abnormality on sonography of

patients with perienteric inlammatory processes. herefore

detection of creeping fat should lead to a detailed evaluation of

the regional gut.

Lymphadenopathy

Tender and enlarged mesenteric and perienteric nodes are

common features of the active phase of inlammation with

Crohn disease (Fig. 8.16). Lymphadenopathy may persist in the

inactive phase. he nodes appear as focal hypoechoic masses

circumferentially surrounding the gut and in the expected

location of the mesenteric attachment. Nodes are frequently

quite round, are of moderate size, and typically lose the normal

linear echogenic streak from the nodal hilum. Similar to the

gut, the lymph nodes show hyperemia as a relection of their

inlammation.

Hyperemia

Mesenteric vascularization and neoangiogenesis are recognized

components of the inlammatory process, and evaluation of blood

low is a useful tool for monitoring inlammatory activity and

response to therapy. Disease activity correlates with hyperemia,

as seen on color Doppler evaluation 28 (Fig. 8.17, Video 8.5).

Although subjective, this addition of color Doppler to gray-scale

sonography can provide valuable supportive evidence of inlammatory

change in the gut and adjacent inlamed fat 21 (see Fig.

8.6B, D, and F). However, color Doppler shows blood low in

major blood vessels with relatively fast-moving blood and does

not show blood low at the perfusion level. To overcome this

limitation of activity assessment, there has been increasing interest

over recent years in the use of CEUS of the bowel, performed

with the injection of microbubble contrast agents. Using ultrasound

quantitative techniques, CEUS allows for objective measurement

of blood low at the perfusion level as a relection of activity.

On observation, we look for transmural enhancement of the

bowel wall and also a “comb sign,” relective of blood low within

the mesenteric vasculature (Fig. 8.18, Videos 8.6 and 8.7).

Generation of time intensity curves allows for measurement of

the peak enhancement and the area under the curve. Studies

have shown a direct correlation between the level of bowel wall

enhancement and active inlammatory disease, as assessed on

colonoscopy. 29,30 Further, Ripollés et al. 29 show that CEUS measurements

perform better than wall thickness in prediction of disease

severity at colonoscopy. In our own laboratory, we have integrated

the objective measurements of blood low on CEUS with the

baseline gray-scale assessments of wall thickness and inlammatory

fat to improve the objectivity of activity assessments on

ultrasound. 23

Mucosal Abnormalities

Although endoscopy remains the major tool for evaluating

mucosal and luminal abnormality, ultrasound may on occasion

show luminal polypoid masses, such as inlammatory polyps,

and deep ulcerations with pockets of echogenic air projecting

within the gut wall. Ultrasound may also show intramural

sinus tracts with air dissecting within the layers of the bowel

wall (Fig. 8.19), as a complication of both Crohn disease and

diverticulitis.

Conglomerate Masses

Conglomerate masses may be related to clumps of matted bowel,

inlamed edematous mesentery, increased fat deposition in the

mesentery, or, infrequently, mesenteric lymphadenopathy. Involved

loops may demonstrate angulation and ixation resulting from

retraction of the thickened ibrotic mesentery.

COMPLICATIONS

Strictures

Strictures are the most common complication of Crohn disease

requiring surgical intervention. hese are due to rigid narrowing

of the gut lumen, contributed to by mural inlammation, ibrosis,

and smooth muscle hypertrophy. he luminal surfaces of involved

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