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ORIGINAL ARTICLE
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Combined hepatocellular cholangiocarcinoma in hepatectomy specimens: A clinicopathologic analysis


1 Department of Pathology, Institute of Liver and Biliary Sciences, New Delhi, India
2 Department of Radiation Oncology, Institute of Liver and Biliary Sciences, New Delhi, India
3 Department of Medical Oncology, Institute of Liver and Biliary Sciences, New Delhi, India
4 Department of Hepatology, Institute of Liver and Biliary Sciences, New Delhi, India
5 Department of Interventional Radiology, Institute of Liver and Biliary Sciences, New Delhi, India
6 Department of Radiology, Institute of Liver and Biliary Sciences, New Delhi, India
7 Department of Biostatistic, Institute of Liver and Biliary Sciences, New Delhi, India
8 Department of HPB and Liver Transplant Surgery, Institute of Liver and Biliary Sciences, New Delhi, India

Correspondence Address:
Archana Rastogi,
Department of Pathology, Institute of Liver and Biliary Sciences, D-1, Vasant Kunj, New Delhi - 110 070
India
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijpm.ijpm_357_22

Background: Combined hepatocellular-cholangiocarcinoma (cHCC-CCA) is an uncommon form of primary liver carcinoma. It is heterogenous in terms of morphology, immunohistochemistry, radiology, and clinical features; making it a challenging entity for diagnosis. Aims: The purpose of the present study was to evaluate clinicopathological characteristics of patients with cHCC-CCA. Settings and Design: Retrospective observational study. Methods and Materials: The patients diagnosed with cHCC-CC were identified from hepatic surgical specimens and were evaluated. Statistical Analysis: Survival was estimated as per Kaplan–Meier method. Results: Out of six patients, five had undergone resection while one had liver transplant. Five were male and one was female and the mean age was 52 years. Tumor markers revealed raised serum alfa-fetoprotein and CA19.9 in four and three patients, respectively. Five of the liver specimens were cirrhotic. Diagnosis was predominantly based on tumor morphology. All cases were of Allen and Lisa type B and cHCC-CCA as per WHO (2019) classification. Stem cell features <5% were noted in two cases. Immunohistochemistry for programmed death 1/programmed death ligand 1 (PD1/PDL1) was negative in both the hepatocellular and cholangiocellular components in all six cases. Mismatch repair (MMR) protein expression was retained in two and deficient in four cases. The median follow-up after surgery was 21.3 months (range, 5-46.2 months). Five patients had intrahepatic and/or extrahepatic recurrence on follow-up after surgery. The median recurrence-free survival was estimated at 13.1 months (95% CI 5.67-20.6). Three patients had received salvage treatment. The median overall survival was estimated at 20 months (95% CI 0-45.3). Conclusions: The present study highlights the role of morphology in the diagnosis of cHCC-CCA. The choice of locoregional and/or systemic therapy after surgery may be individualized based on the clinicopathological characteristics.


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    -  Patil N
    -  Sahai P
    -  Rastogi A
    -  Sharma N
    -  Shasthry SM
    -  Mukund A
    -  Laroia ST
    -  Kumar G
    -  Pamecha V
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