Purpose
The cHCC-CC is a rare variant of primary liver cancers (0.87%–4.7%),
comprising elements of both hepatocellular carcinoma (HCC) and cholangiocarcinoma (CC).
The history of cHCC-CC's classification started in 1949,
with Allen and Lisa that described cHCC-CC and classified it into three subtype.
Type A or "double cancer" represents cases in which HCC and CC exist separately; type B,
"combined" type,
HCC and CC components exist contiguously,
but independently; and type C,
"mixed" type,
occurs when HCC and CC components are admixed within a mass.
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Methods and Materials
Study Population
The database of the Department of Pathology from December 2004 to January 2012 was cross-referenced with the database of Departement of Radiology to identify all patients with pathology-confirmed diagnosis of cHCC-CC who had undergone MRI and CT.
This retrospective study includes nine patients (eight male,
one female,
mean age 54.8 years,
range 42–70 years)who had either an hepatectomy (n=3) or a core biopsy (n=1) for HCC and CC,
either a liver transplantation (LT) (n=5) for HCC.
All the patients were evaluated with presurgical...
Results
Histopathology
The cHCC-CC is a "mixed" type in 6/9 patients and "combined" typein 3/9 patients.
Serum markers
The AFP serum level was elevated in 5/9 but only one up to 200 ng/mL and the CA19-9 serum level was elevated in 2/3 patient.
These 2 patients have also an AFP serum level elavated.
Morphologic imaging findings
The cHCC-CC tumor presented as a single mass in allpatients,
measuring from 1.5 to 10 cm on the axial plane (mean size 41 mm).
All the cHCC-CC were 6/9 localized...
Conclusion
In conclusion,
the imaging appearance of cHCC-CC is commonly a solitary mass,
heterogeneous,
hyperintense on T2-w in cirrhotic patients.
In half of the case,
after dynamic injection,
cHCC-CC look likes HCC and the other half look like CC.
This diagnosis could not be based on imaging alone.
The combination of both elevated serum tumor markers may help in the diagnosis.
The definitive diagnosis of cHCC-CC requires demonstration of both hepatocellular and cholangiocellulardifferentiation at histopathology analysis,
which is usually facilitated by immunohistochemical and special stains to...
References
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Yeh MM.
Pathology of combined hepatocellular-cholangiocarcinoma.
J Gastroenterol Hepatol 2010;25:1485–1492.
2.
Allen RA,
Lisa JR.
Combined liver cell and bile duct carcinoma.
Am J Pathol 1949;25:647–655.
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Kim H,
Park C,
Han H-K et al.
“Primary liver carcinoma of intermediate (hepatocyte-cholangiocyte) phenotype,”Journal of Hepatology,vol.
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Zhang F,
Chen X-P,
Zhang W et al.
“Combined hepa- tocellular cholangiocarcinoma originating from hepatic pro- genitor cells: immunohistochemical and double-fluorescence immunostaining evidence,”Histopathology,vol.
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Kassahun WT,
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Personal Information
Dr.
Nicola Leo
Radiology
Hospital Paul Brousse
Villejuif,
Paris,
FRANCE
Email:
[email protected]
Special thanks to SIAD