Point-of-Care Ultrasound Techniques for the Small Animal Practitioner. Группа авторов. Читать онлайн. Newlib. NEWLIB.NET

Автор: Группа авторов
Издательство: John Wiley & Sons Limited
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Жанр произведения: Биология
Год издания: 0
isbn: 9781119461029
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The size is variable depending on when gallbladder contraction last occurred. In the typical normal state, the gallbladder is an anechoic structure with a uniformly thin echogenic wall. Normal gallbladder wall thickness is less than 1 mm in cats and less than 3 mm in dogs (Hittmair et al. 2001; Spaulding 1993); however, for all intents and purposes, the gallbladder wall should be a thin white line in both species (Figure 8.4A–C; see also Figure 8.11). Gallbladder sludge (echogenic gravity‐dependent material within the lumen) is common in dogs and generally a benign finding in the absence of other significant ultrasonographic and clinical findings although the presence of “normal” gallbladder sludge has been more recently questioned (Tsukagoshi et al. 2012) (see Figure 8.12A–D). The finding may be an indication of cholestasis. The intrahepatic bile ducts are not seen unless there is extrahepatic biliary obstruction of at least five days’ duration when the fluid dilated ducts will have the appearance of hepatic veins (without the hyperechoic walls of portal veins) (see Figure 8.15A,B). If available, color flow Doppler is useful for differentiating the lack of flow in a dilated biliary duct from the normal blood flow in hepatic and portal vessels; however, tracing structures in real time is often adequate. The common bile duct is small and difficult to see in the normal state in dogs and cats, but is generally easier to identify in the cat.

      Pearl: It may be difficult to tell the difference between a dilated biliary tract (no flow) and hepatic veins (flow), in which case color flow Doppler may be helpful.

      Artifacts are commonly encountered when performing the POCUS liver and gallbladder examination and include mirror image, acoustic enhancement, side‐lobe, slice thickness, and edge shadowing. These are discussed in more detail in Chapter 3 and 5.

       Mirror image. The most common of these artifacts results in a mirror image of the liver and gallbladder being seen on the far side of the lung–diaphragm interface. This should not be mistaken for a diaphragmatic hernia (see Figure 8.9D).

       Acoustic enhancement. Acoustic enhancement is associated with a fluid‐filled gallbladder that causes an increase in echogenicity of the hepatic parenchyma on the far side of the gallbladder. Acoustic enhancement should not be mistaken for increased liver echogenicity.

       Side‐lobe and slice thickness. These artifacts involve fluid‐filled organs like the gallbladder and give the false impression of the presence of luminal sediment.

       Edge shadowing. This artifact also involves fluid‐filled organs like the gallbladder and gives the appearance of a defect in the wall that can be mistaken for gallbladder rupture or gallbladder wall mineralization.

      Pearl: Common artifacts in the liver include mirror image, acoustic enhancement, side‐lobe, slice thickness, and edge shadow.

      Goals of POCUS liver and gallbladder examination include recognition of liver masses (single, multifocal), obvious changes in liver echogenicity, hepatic venous congestion, identification of gallbladder wall abnormalities and gallbladder luminal conditions, and recognition of signs of biliary obstruction. Such findings should prompt referral for a complete detailed abdominal ultrasound as interventions may be indicated.

       Liver Masses

      Identification of focal liver masses is the easiest task to learn with the POCUS examination. It is important to remember that is not possible to differentiate between benign and malignant processes based on ultrasound alone. Focal lesions may be caused by regenerative nodules or nodular hyperplasia, benign or malignant neoplasia, focal inflammatory disease (e.g., abscesses and granulomas), cysts, and hematomas.

      The origin of a large midabdominal mass can sometimes be difficult to determine when the mass contacts multiple origins. In this case, try repositioning the patient from dorsal to lateral recumbency. This will often separate the liver and spleen from one another and help determine the origin of the mass. Generally, the spleen is differentiated from the liver by its hyperechoic capsule (bright white) and its vasculature splitting its capsule unlike the liver.

       Benign hepatic nodular disease is common and nodules associated with nodular hyperplasia may be variable in echogenicity when compared to normal hepatic parenchyma (hyperechoic, hypoechoic, isoechoic or mixed echogenicity). Generally, well‐defined hyperechoic homogeneous nodules are more likely to be benign but cytology or histopathology is necessary for definitive evaluation. Nodular hyperplasia is common in older dogs (Nyland et al. 2002) (Figure 8.5).

       Hepatic cysts consist of round to oval anechoic (fluid‐filled) structures with well‐defined walls. These are generally benign unless a significant amount of hepatic architecture is disrupted and there is evidence of hepatic dysfunction (polycystic disease). Cysts may be parenchymal or biliary in nature, and may be congenital or acquired. Cysts that have irregular margins or contain echogenic material are less likely to be benign and may represent abscesses, inflammation or neoplastic changes (Figure 8.6A–C).

       Other parenchymal masses may have variable appearances and include abscess, hematoma, nodular hyperplasia and neoplasia.

       Hepatic abscesses are uncommon, usually indistinguishable from nodules and mass lesions of other etiology, and may have variable echogenicity, appearance, and margination (Figure 8.7A). Most commonly, abscesses are relatively hypoechoic, thick‐walled lesions which may have cystic or cavitary components or mixed echogenicity. A more definitive finding is the presence of gas (due to gas‐forming bacteria) within the lesion, which appears as focal areas of hyperechogenicity with distal edge shadowing, comet tailing, and reverberation. Fine needle aspiration with cytology and microbial culture and sensitivity is helpful in confirming the diagnosis. However, neoplastic lesions can have necrotic centers that can be mistaken for abscesses and therefore, diagnosis should always be in conjunction with additional clinical findings that support the diagnosis. The Global FAST approach is helpful as a quick screening test for disseminated versus localized disease and the presence or absence of lung nodules (quick pulmonary metastasis check).Figure 8.5. Nodular hyperplasia. (A) Small hyperplastic nodule as demarcated by the caliper marks made by the sonographer, consistent histopathologically