C‑KIT‑positive undifferentiated tumor of the liver: A case report
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- Published online on: July 8, 2014 https://doi.org/10.3892/ol.2014.2324
- Pages: 1665-1669
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Abstract
With recent advances in cancer stem cell analysis, it has been postulated that the transformation of hepatic stem and progenitor cells underlies the development of certain liver cancers. Human C‑KIT is a transmembrane type III receptor protein with intrinsic tyrosine kinase activity that has been proposed as a marker for human embryonic stem cells. In addition, human C‑KIT functions in maintaining the undifferentiated state of stem cells, and has been identified as a marker for human hematopoietic and hepatic stem/progenitor cells. The present study identified an unusual case of a C‑KIT‑positive hepatic tumor with an undifferentiated stem cell phenotype distinct from existing descriptions of liver tumors. A 69‑year‑old male with Ampulla of Vater (AoV) cancer was admitted to the hospital for the treatment of a hepatic mass that was incidentally detected during evaluation of AoV cancer. Microscopically, the hepatic tumor was composed of solidly packed small, round and uniform undifferentiated cells, which resembled that of a small‑blue‑round‑cell tumor. The immunophenotype of neoplastic cells (C‑KIT+/EpCAM+/E‑cadherin+/keratin 7‑/keratin 19‑/α‑fetoprotein‑/albumin‑) supported primitive stem cell features with no hepatic or biliary phenotypes. Polymerase chain reaction and direct DNA sequencing revealed no C‑KIT mutations. It is suggested that this tumor may have originated from transformed C‑KIT+/EpCAM+/E‑cadherin+ cells, which are more primitive and undifferentiated than bipotential hepatic progenitor cells.
