Hepatocellular adenoma with a double mutation HNF1A and IDH1 in a patient with Ollier disease
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DOI: 10.1111/liv.15066
Abstract: Somatic mutations in isocitrate dehydrogenase1 (IDH1) gene1-3 are common in Ollier disease and in several neoplasms including cholangiocarcinoma. We report the case of a woman with Ollier disease with chondrosarcomas and an anaplastic astrocytoma. A mutation in IDH1 was… read more here.
Keywords: adenoma double; ollier disease; patient; hepatocellular adenoma ... See more keywords