Case Report
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 15, 2003; 9(3): 627-630
Published online Mar 15, 2003. doi: 10.3748/wjg.v9.i3.627
Concomitant hepatocellular adenoma and adenomatous hyperplasia in a patient without cirrhosis
Chuan-Yuan Hsu, Cheng-Hsin Chu, Shee-Chan Lin, Fee-Shih Yang, Tsen-Long Yang, Kuo-Ming Chang
Chuan-Yuan Hsu, Cheng-Hsin Chu, Shee-Chan Lin, Department of Hepatology & Gastroenterology, Mackay Memorial Hospital, Taipei, Taiwan, China
Fee-Shih Yang, Department of Radiology, Mackay Memorial Hospital, Taipei, Taiwan, China
Tsen-Long Yang, Department of Surgery, Mackay Memorial Hospital, Taipei, Taiwan, China
Kuo-Ming Chang, Department of Pathology, Mackay Memorial Hospital, Taipei, Taiwan, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Chuan-Yuan Hsu, Department of Hepatology & Gastroenterology, Mackay Memorial Hospital, No. 92, Chung-Shan N. Road 2 Section, 104 Chung-Shan Area, Taipei, Taiwan, China. erichsu@ms1.mmh.org.tw
Telephone: +886-2-25433535
Received: November 29, 2002
Revised: December 15, 2002
Accepted: December 22, 2002
Published online: March 15, 2003
Abstract

AIM: Hepatocelluar adenoma (HCA) and adenomatous hyperplasia (AH) are rare benign tumors of the liver. HCA is usually found in women who use oral contraceptives. AH usually occurs in patients with liver cirrhosis. Both tumors have potential for malignant transformation.

METHODS: We described a male adult with chronic liver disease (CLD) who had been known to be a hepatitis B carrier (HBV) for years. He was found to have a space-occupying lesion with a suspicion of hepatocellular carcinoma (HCC) by abdominal ultrasonography. His α-fetoprotein (AFP) was normal. Angiographic findings were consistent with the diagnosis of HCC, he wished to avoid an operation, was treated with transcatheter hepatic arterial embolization.

RESULTS: He subsequently consented to surgery, and a right lobectomy was performed. The liver pathology disclosed HCA with nuclear dysplasia and post-embolization effects. In addition, there were multiple small foci of AH with nuclear dysplasia in the resected liver. Although he had some focal areas of cirrhosis-like change or post-embolization effect, the AH was associated only with normal liver tissue.

CONCLUSION: This case confirms that HCA and AH may resemble HCC on imaging studies, and that AH may occur in CLD in the absence of cirrhotic change.

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