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5.5




            Pancreas


















            The  canine  and feline  pancreas  is  readily  visible  on   Inflammatory disorders
            unenhanced and contrast‐enhanced CT images and on
            MR images. CT is preferred because of faster scanning   Acute pancreatitis has been diagnosed using CT imag­
            times and the ability to eliminate motion artifact when   ing in dogs and cats (Figures 5.5.4, 5.5.5). The pancreas
            viewing the thin tissue of the pancreas. However, MR   is enlarged with irregular borders and is intensely con­
            has increased contrast resolution and provides excellent   trast enhancing. Regions of hypoattenuation may be
            information in inflammatory diseases, such as chronic   present in necrotic regions. The surrounding mesentery
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            pancreatitis. 1                                    has fat stranding secondary to local inflammation.
               The normal feline pancreatic thickness on T1 images is   Chronic pancreatitis resulting in fibrosis and fat replace­
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            9.5 ± 1.2 mm, and pancreatic duct size is 1.65 ± 0.05 mm.    ment may be hypoattenuating and poorly contrast
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            The  pancreas  is T1  hyperintense  and T2 hypointense   enhancing (Figures 5.5.6, 5.5.7).  Nodular regions and
            compared to the liver, with a uniform architecture. The   mild enlargement without surrounding mesenteric
            feline pancreatic duct is oriented in the long axis of each   inflammation are characteristic of chronic pancreatitis.
            lobe and may be visualized as a hypoattenuating (CT),   Pancreatitis is a challenging disease to diagnose in cats
            hypointense (T1), or hyperintense (T2, FSE) linear struc­  using ultrasound and CT. MR imaging shows promise in
            ture. The feline pancreas is hypoattenuating to liver on   detecting these changes with increased tissue contrast
            unenhanced CT images, with rapid contrast enhance­  and 3D volume imaging. Pancreatitis appears as T1
                                                3
            ment and gradual washout (Figure 5.5.1).  CT imaging   hypointensity and T2 hyperintensity with pancreatic
            features of the canine pancreas are similar (Figure 5.5.2).  duct dilation. The signal intensity changes are likely
              Multiphase CT angiography allows the evaluation of   caused by edema and fibrosis. Administration of secretin
            pancreatic tissues in the native, arterial, portal, and   can be used to dilate the pancreatic duct. This improves
            delayed phases of contrast enhancement. The canine   visualization of the pancreatic duct in normal cats; how­
            pancreas is isoattenuating to liver on unenhanced images,   ever, in those with pancreatitis, it causes only minimal
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            hyperattenuating on arterial phase images, and hypoat­  change to ducts that are already dilated.  Unenhanced
            tenuating on portal and delayed phase images. The atten­  and contrast‐enhanced CT images cannot consistently
            uation differences are due to the purely arterial blood   differentiate normal cats from those with pancreatitis
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            supply of the pancreas, which results in rapid enhance­  unless there is marked pancreatic enlargement.
            ment following injection of contrast medium, compared   Complications of pancreatitis in both species
            to the predominantly portal enhancement of the liver.   include formation of pseudocysts, abscesses, and
            The pancreaticoduodenal artery is visible during the   necrosis. Pancreatic cysts and pseudocysts can also
            arterial phase, and the pancreaticoduodenal vein opaci­  occur as incidental findings (Figure  5.5.8). On CT
            fies during the portal and delayed phases (Figure 5.5.3). 4  images, pseudocysts and abscesses appear fluid



            Atlas of Small Animal CT and MRI, First Edition. Erik R. Wisner and Allison L. Zwingenberger.
            © 2015 John Wiley & Sons, Inc. Published 2015 by John Wiley & Sons, Inc.
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