Abstract

BackgroundCombined hepatocellular-cholangiocarcinoma (cHCC-CCA) is a primary liver carcinoma with both hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA) components. We examined the clinicopathological characteristics and recurrence patterns of cHCC-CCA. Because of the rarity of cHCC-CCA, its etiology, clinicopathological features, and prognosis in comparison with other primary liver carcinoma remain unknown. Its recurrence pattern and sites in particular also need to be elucidated.MethodsAll patients who underwent hepatectomy for primary liver malignancies between 2005 and 2015 were retrospectively included in this study.ResultsEight hundred and ninety-four hepatectomies were performed. Nineteen cases of cHCC-CCA (2.1%) in 16 patients were enrolled. Three patients underwent re-hepatectomy. The background of hepatitis viruses and tumor marker patterns of cHCC-CCA were similar to those of HCC and dissimilar to those of intrahepatic CCA (iCCA). Biliary invasion was common in cHCC-CCA and iCCA. The 5-year overall survival values of the cHCC-CCA, HCC, and iCCA patients were 44.7%, 56.6%, and 38.5%, respectively. The 5-year recurrence-free survival values of the cHCC-CCA, HCC, and iCCA patients were 12.2%, 28.7%, and 32.9%, respectively. The liver was the most common recurrence site. Unlike HCC, however, the lymph node was the second-most common recurrence site in both cHCC-CCA and iCCA. Pathological samples of the recurrent lesions were obtained in six patients, and four had cHCC-CCA recurrence pathologically.ConclusioncHCC-CCA had a mixture of characteristics of HCC and iCCA. Many cases of cHCC-CCA remained cHCC-CCA pathologically even after recurrence.

Highlights

  • Combined hepatocellular-cholangiocarcinoma is a relatively rare primary liver carcinoma that has both a hepatocellular carcinoma (HCC) component and cholangiocarcinoma (CCA) component in the same tumor nodule [1]

  • We examined the clinicopathological characteristics and recurrence patterns of cHCCCCA patients who underwent hepatectomy in a single institution

  • Sixteen patients with cHCC-CCAs accounted for 19 cases that received hepatectomy (2.1%); 3 of the 16 cHCC-CCA patients underwent repeated hepatectomy (15.8%)

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Summary

Introduction

Combined hepatocellular-cholangiocarcinoma (cHCCCCA) is a relatively rare primary liver carcinoma that has both a hepatocellular carcinoma (HCC) component and cholangiocarcinoma (CCA) component in the same tumor nodule [1]. Because of the rarity of cHCC-CCA, its etiology and clinicopathological features in comparison with other primary liver carcinoma remain unknown [5,6,7,8,9,10,11]. The prognosis of cHCC-CCA is often reported to be worse than that of HCC, the prognostic outcomes vary in comparison with that of iCCA [5, 8]. We examined the clinicopathological characteristics and recurrence patterns of cHCC-CCA. Because of the rarity of cHCC-CCA, its etiology, clinicopathological features, and prognosis in comparison with other primary liver carcinoma remain unknown. Its recurrence pattern and sites in particular need to be elucidated

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