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@ARTICLE{Roner:212427,
author = {F. Roßner and B. V. Sinn and D. Horst$^*$},
title = {{P}athology of {C}ombined {H}epatocellular
{C}arcinoma-{C}holangiocarcinoma: {A}n {U}pdate.},
journal = {Cancers},
volume = {15},
number = {2},
issn = {2072-6694},
address = {Basel},
publisher = {MDPI},
reportid = {DKFZ-2023-00146},
pages = {494},
year = {2023},
abstract = {Combined hepatocellular carcinoma-cholangiocarcinoma
(cHCC-CCA) is a rare primary liver cancer that is composed
of both hepatocellular and cholangiocellular differentiated
cells. It is slightly more common in men and among Asian and
Pacific islanders. Overall, risk factors are similar to
classic risk factors of hepatocellular carcinoma (HCC). The
classification has significantly evolved over time. The last
WHO classification (2019) mainly emphasized diagnosis on
morphological basis with routine stainings, discarded
previously recognized classifications with carcinomas with
stem cell features, introduced intermediate cell carcinoma
as a specific subtype and considered cholangiolocarcinoma as
a subtype of cholangiocellular carcinoma.
Immunohistochemical markers may be applied for further
specification but have limited value for diagnosis. Recent
discoveries in molecular pathway regulation may pioneer new
therapeutic approaches for this poor prognostic and
challenging diagnosis.},
subtyp = {Review Article},
keywords = {cHCC-CCA (Other) / cholangiocarcinoma (Other) / combined
hepatocellular and cholangiocellular carcinoma (Other) /
hepatocellular carcinoma (Other) / hippo signaling (Other) /
mixed carcinoma (Other) / progenitor cells (Other) / stem
cells (Other) / wnt signaling (Other)},
cin = {BE01},
ddc = {610},
cid = {I:(DE-He78)BE01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:36672443},
pmc = {pmc:PMC9856551},
doi = {10.3390/cancers15020494},
url = {https://inrepo02.dkfz.de/record/212427},
}