Skip to main content

Advertisement

Log in

Dynamic changes in ultrasound characteristics of nodules in cirrhotic liver and their implications in surveillance for malignancy

  • Original Article
  • Published:
Journal of Medical Ultrasonics Aims and scope Submit manuscript

Abstract

Objective

To investigate whether there are ultrasound characteristics that can suggest HCC in ultrasound surveillance of nodules in cirrhotic liver.

Methods

Data from 277 patients with hepatitis B virus-related nodules in cirrhotic liver undergoing ultrasound surveillance of the nodules for malignancy were reviewed. Size of the nodules ranged 6–23 mm. The nodules were followed by color Doppler ultrasound at 3- to 6-month intervals, with focus on size, shape, echogenicity, margin, halo sign, and vasculature. Suspicious malignant nodules underwent contrast-enhanced CT/MRI, and some indeterminate nodules underwent biopsy.

Results

Nodules in 189 patients were hypo/isoechoic/faint high echoic, 23 were hyperechoic, and 65 were both hypo/isoechoic/faint high echoic and hyperechoic. Forty-two patients developed hepatocellular carcinoma: 35 from nodules and 7 from background parenchyma. Fourteen nodules recessed (size >10 mm), 11 new nodules emerged (size >10 mm), and the total number of nodules increased over 5 years. All hepatocellular carcinomas developed from hypo/isoechoic/faint high echoic nodules, and no typical hyperechoic nodules developed into hepatocellular carcinomas. The size increased significantly when the nodules developed into hepatocellular carcinomas. No nodule presented an overt halo, seven hepatocellular carcinomas developed from nodules with a halo, and ill-defined margins of 16 nodules became well defined when they developed into hepatocellular carcinomas. No vasculature was detectable in the nodules, while it was detectable in eight hepatocellular carcinomas. No significant change occurred in nodules without malignancy.

Conclusion

The characteristics for dynamic surveillance of nodules in cirrhotic liver for malignancy should include nodule growth, margin, halo, and vasculature. Apart from evident growth, an ill-defined margin becoming a well-defined margin, a newly emerged halo, and newly detectable vasculature are strongly suggestive of nodule malignancy.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Della Corte C, Colombo M. Surveillance for hepatocellular carcinoma. Semin Oncol. 2012;39:384–98.

    Article  PubMed  Google Scholar 

  2. Shah TU, Semelka RC, Pamuklar E, et al. The risk of hepatocellular carcinoma in cirrhotic patients with small liver nodules on MRI. Am J Gastroenterol. 2006;101:533–40.

    Article  PubMed  Google Scholar 

  3. Seki S, Sakaguchi H, Kitada T, et al. Outcomes of dysplastic nodules in human cirrhotic liver: a clinicopathological study. Clin Cancer Res. 2000;6:3469–73.

    CAS  PubMed  Google Scholar 

  4. Rapaccini GL, Pompili M, Caturelli E, et al. Hepatocellular carcinomas < 2 cm in diameter complicating cirrhosis: ultrasound and clinical features in 153 consecutive patients. Liver Int. 2004;24:124–30.

    Article  PubMed  Google Scholar 

  5. Ignee A, Weiper D, Schuessler G, et al. Sonographic characterisation of hepatocellular carcinoma at time of diagnosis. Z Gastroenterol. 2005;43:289–94.

    Article  CAS  PubMed  Google Scholar 

  6. Min YW, Gwak GY, Lee MW, et al. Clinical course of sub-centimeter-sized nodules detected during surveillance for hepatocellular carcinoma. World J Gastroenterol. 2012;18:2654–60.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  7. Furlan A, Marin D, Agnello F, et al. Hepatocellular carcinoma presenting at contrast-enhanced multi-detector-row computed tomography or gadolinium-enhanced magnetic resonance imaging as a small (≤ 2 cm), indeterminate nodule: growth rate and optimal interval time for imaging follow-up. J Comput Assist Tomogr. 2012;36:20–5.

    Article  PubMed  Google Scholar 

  8. Bruix J, Sherman M. Management of hepatocellular carcinoma: an update. Hepatology. 2011;53:1020–2.

    Article  PubMed Central  PubMed  Google Scholar 

  9. Songdo S, Bae SH. Changes of guidelines diagnosing hepatocellular carcinoma during the last ten-year period. Clin Mol Hepatol. 2012;18:258–67.

    Article  Google Scholar 

  10. Wernecke K, Vassallo P, Bick U, et al. The distinction between benign and malignant liver tumors on sonography: value of a hypoechoic halo. AJR Am J Roentgenol. 1992;159:1005–9.

    Article  CAS  PubMed  Google Scholar 

  11. Cosgrove D. Angiogenesis imaging–ultrasound. Br J Radiol. 2003;76:S43–9.

    Article  PubMed  Google Scholar 

  12. Furuse J, Iwasaki M, Yoshino M, et al. Evaluation of blood flow signal in small hepatic nodules by color Doppler ultrasonography. Jpn J Clin Oncol. 1996;26:335–40.

    Article  CAS  PubMed  Google Scholar 

  13. Borzio M, Borzio F, Croce A, et al. Ultrasonography-detected macroregenerative nodules in cirrhosis: a prospective study. Gastroenterology. 1997;112:1617–23.

    Article  CAS  PubMed  Google Scholar 

  14. Yoshimitsu K, Irie H, Aibe H, et al. Pitfalls in the imaging diagnosis of hepatocellular nodules in the cirrhotic and noncirrhotic liver. Intervirology. 2004;47:238–51.

    Article  PubMed  Google Scholar 

  15. Kim KW, Kim MJ, Lee SS, et al. Sparing of fatty infiltration around focal hepatic lesions in patients with hepatic steatosis: sonographic appearance with CT and MRI correlation. AJR Am J Roentgenol. 2008;190:1018–27.

    Article  PubMed  Google Scholar 

  16. Colagrande S, Paolucci ML, Messerini L, et al. Solitary necrotic nodules of the liver: cross-sectional imaging findings and follow-up in nine patients. AJR Am J Roentgenol. 2008;191:1122–8.

    Article  PubMed  Google Scholar 

  17. Lee JW, Kim S, Kwack SW, et al. Hepatic capsular and subcapsular pathologic conditions: demonstration with CT and MR imaging. Radiographics. 2008;28:1307–23.

    Article  PubMed  Google Scholar 

  18. Kim S, Maekawa Y, Matsuoka T, et al. Eosionophilic pseudotumor of the liver due to Ascaris suum infection. Hepatol Res. 2002;23:306.

    Article  PubMed  Google Scholar 

Download references

Conflict of interest

The authors declare there are no financial or other relations that could lead to a conflict of interest.

Human rights statements and informed consent

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008 (5). Informed consent was waived by all patients for being included in the retrospective study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Size Wu.

About this article

Cite this article

Wu, S., Tu, R., Liu, G. et al. Dynamic changes in ultrasound characteristics of nodules in cirrhotic liver and their implications in surveillance for malignancy. J Med Ultrasonics 41, 165–171 (2014). https://doi.org/10.1007/s10396-013-0494-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10396-013-0494-8

Keywords

Navigation