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Intrahepatic Clear Cell Cholangiocarcinoma - An Uncommon Histologic Subtype: Case Report and Literature Review

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Rev Esp Enferm Digest 2017.pdf1.42 MBAdobe PDF Download

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Abstract(s)

Clear-cell cholangiocarcinoma is a very uncommon variant of cholangiocarcinoma with a largely unknown natural history and prognosis. We report a case of a 51-year-old previously healthy woman presenting with a large liver nodule found on routine imaging. Needle biopsy of the lesion suggested a non-hepatocellular carcinoma. After extensive workup for other primary neoplasms, the patient underwent a partial hepatectomy. Histopathology was compatible with a moderately differentiated clear-cell cholangiocarcinoma. There was no evidence of liver disease in the remaining tissue. The patient underwent chemotherapy and remains in clinical remission after two years.

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CHLC CHBPT Adenocarcinoma, Clear Cell/diagnosis Adenocarcinoma, Clear Cell/pathology Bile Duct Neoplasms/diagnosis Bile Duct Neoplasms/pathology Bile Ducts, Intrahepatic/pathology Cholangiocarcinoma/diagnosis Cholangiocarcinoma/pathology

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Rev Esp Enferm Dig. 2017 May;109(5):382-385

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Sociedad Española de Patologia Digestiva

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