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RID: RID39486

Washout appearance

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Definition:

Usage:

  • Applies to: Observations that, by visual assessment, appear to “washout” in whole or in part
    • Type of feature: Major
    • How it should be assessed or characterized:
      • Delayed phase preferred over venous phase.
      • Rational: Delayed phase may be superior to portal venous phase for depicting washout appearance. Some observations may show washout appearance only in the delayed phase.
      • The enhancement of the observation should be compared to that of the adjacent liver parenchyma. If the liver parenchyma visually consists of both nodules and fibrosis, then enhancement of the observation should be compared to that of the composite liver tissue (i.e., a visual average of the nodules and fibrosis)

If unsure about feature:

  • Do not characterize as washout appearance.

 Synonyms:

  • Synonyms: Washout, Venous or delayed phase washout.
  • Preferred terms: Washout appearance and “washout” (with quotation marks) are preferred over the term washout.
  • Rationale for preferred terms: The visually assessed temporal reduction in enhancement relative to liver may be due to progressive enhancement of the liver rather than actual de-enhancement of the observation.

Background

  • Washout appearance is a LI-RADS major feature for categorization of masses that are neither definite benign entities nor probable benign entities and that lack features of non-HCC malignancy or tumor in vein. For such masses, those with washout appearance may be categorized LR-3, LR-4, or LR-5, depending on the observation’s arterial phase enhancement, diameter, and other features.
  • Washout appearance is also an imaging feature used in both AASLD guidelines and OPTN policy for the imaging diagnosis of HCC

Potential pitfalls and challenges

  • As washout appearance is assessed visually, LI-RADS does not mandate objective assessment using ROI measurements, time-enhancement curves, or subtraction images.
  • Radiologists at their discretion may use ROI measurements, time-enhancement curves, or, at MRI, subtraction images (e.g., arterial phase minus portal venous or delayed phase) to evaluate “washout”.
  • For ROI measurements, time-enhancement curves, or subtractions to be valid, arterial phase and portal venous or delayed phase images need to be acquired with the same technique. In addition, subtractions require co-registration of the source images.
  • Washout can be present in only part of the observation.  The component with washout does not need to correspond to the component that demonstrates arterial hyperenhancement, however the component does need to enhance for this feature to be present. 
    • Washout of the periphery of an observation, however, should be characterized as peripheral washout rather than washout appearance. Washout of the periphery of an observation is a finding suggestive of intrahepatic cholangiocarcinoma rather than HCC.  Peripheral washout is not a major feature and its presence favors a category of LR-M rather than LR-3, LR-4, or LR-5.
  • Washout may be difficult to assess in patients with diffuse hepatic fat deposition. In this instance, subtraction images may be helpful.
  • Hepatobiliary phase hypointensity is not considered washout appearance. Washout appearance should only be assessed during the portal venous phase of enhancement with gadoxetate disodium, prior to the transitional or hepatobiliary phases.
  • In individuals with normal hepatic function, some hepatocellular uptake of gadoxetic acid may be evident in the portal venous phase; therefore, in at risk patients with relatively preserved hepatic function, hepatocyte uptake in the portal venous phase potentially could result in a “pseudo-washout appearance”, although no studies to date have documented this potential pitfall.
  • Hypointensity in the transitional phase can be present in non-hepatocellular lesions (metastases, hemangiomas, cholangiocarcinomas) due to the above described enhancement of the liver parenchyma and lack of transporter expression.  This finding should be considered pseudo-washout rather than washout appearance.  

References:

1.         Kim, T.K., et al., Analysis of gadobenate dimeglumine-enhanced MR findings for characterizing small (1-2-cm) hepatic nodules in patients at high risk for hepatocellular carcinoma. Radiology, 2011. 259(3): p. 730-8.

2.         Cereser, L., et al., Comparison of portal venous and delayed phases of gadolinium-enhanced magnetic resonance imaging study of cirrhotic liver for the detection of contrast washout of hypervascular hepatocellular carcinoma. J Comput Assist Tomogr, 2010. 34(5): p. 706-11.

3.         Lim, J.H., et al., Detection of hepatocellular carcinomas and dysplastic nodules in cirrhotic livers: accuracy of helical CT in transplant patients. AJR Am J Roentgenol, 2000. 175(3): p. 693-8.

4.         Forner, A., et al., Diagnosis of hepatic nodules 20 mm or smaller in cirrhosis: Prospective validation of the noninvasive diagnostic criteria for hepatocellular carcinoma. Hepatology, 2008. 47(1): p. 97-104.

5.         Sangiovanni, A., et al., The diagnostic and economic impact of contrast imaging techniques in the diagnosis of small hepatocellular carcinoma in cirrhosis. Gut, 2010. 59(5): p. 638-44.

6.         Monzawa, S., et al., Dynamic CT for detecting small hepatocellular carcinoma: usefulness of delayed phase imaging. AJR Am J Roentgenol, 2007. 188(1): p. 147-53.

7.         Lee, J.H., et al., Enhancement patterns of hepatocellular carcinomas on multiphasicmultidetector row CT: comparison with pathological differentiation. Br J Radiol, 2012. 85(1017): p. e573-83.

8.         Furlan, A., et al., Hepatocellular carcinoma in cirrhotic patients at multidetector CT: hepatic venous phase versus delayed phase for the detection of tumour washout. Br J Radiol, 2011. 84(1001): p. 403-12.

9.         Witjes, C.D., et al., Histological differentiation grade and microvascular invasion of hepatocellular carcinoma predicted by dynamic contrast-enhanced MRI. J Magn Reson Imaging, 2012. 36(3): p. 641-7.

10.       Kim, M.J., et al., Imaging features of small hepatocellular carcinomas with microvascular invasion on gadoxetic acid-enhanced MR imaging. Eur J Radiol, 2012. 81(10): p. 2507-12.

11.       Leoni, S., et al., The impact of vascular and nonvascular findings on the noninvasive diagnosis of small hepatocellular carcinoma based on the EASL and AASLD criteria. Am J Gastroenterol, 2010. 105(3): p. 599-609.

12.       Marrero, J.A., et al., Improving the prediction of hepatocellular carcinoma in cirrhotic patients with an arterially-enhancing liver mass. Liver Transpl, 2005. 11(3): p. 281-9.

13.       Luca, A., et al., Multidetector-row computed tomography (MDCT) for the diagnosis of hepatocellular carcinoma in cirrhotic candidates for liver transplantation: prevalence of radiological vascular patterns and histological correlation with liver explants. Eur Radiol, 2010. 20(4): p. 898-907.

14.       Rimola, J., et al., Non-invasive diagnosis of hepatocellular carcinoma </= 2 cm in cirrhosis. Diagnostic accuracy assessing fat, capsule and signal intensity at dynamic MRI. J Hepatol, 2012. 56(6): p. 1317-23.

15.       Kim, S.E., et al., Noninvasive diagnostic criteria for hepatocellular carcinoma in hepatic masses >2 cm in a hepatitis B virus-endemic area. Liver Int, 2011. 31(10): p. 1468-76.

16.       Khalili, K., et al., Optimization of imaging diagnosis of 1-2 cm hepatocellular carcinoma: an analysis of diagnostic performance and resource utilization. J Hepatol, 2011. 54(4): p. 723-8

17.       Yu, J.S., et al., Small hypervascular hepatocellular carcinoma: limited value of portal and delayed phases on dynamic magnetic resonance imaging. Acta Radiol, 2008. 49(7): p. 735-43.

18.       Yu, J.S., et al., Small hypervascular hepatocellular carcinomas: value of "washout" on gadolinium-enhanced dynamic MR imaging compared to superparamagnetic iron oxide-enhanced imaging. Eur Radiol, 2009. 19(11): p. 2614-22. 

19.       Khan, A.S., et al., Value of delayed hypointensity and delayed enhancing rim in magnetic resonance imaging diagnosis of small hepatocellular carcinoma in the cirrhotic liver. J Magn Reson Imaging, 2010. 32(2): p. 360-6. 




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