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A case of primary carcinosarcoma of the liver with combined hepatocellular carcinoma and cholangiocarcinoma.

Takashi OfuchiKatsunori ImaiYosuke NakaoShigeki NakagawaYuta ShiraishiRikako KatoRumi ItoyamaToshihiko YusaTakaaki HigashiHiromitsu HayashiTsuguharu AsatoYo-Ichi YamashitaYoshiki MikamiHideo Baba
Published in: Clinical journal of gastroenterology (2021)
Primary carcinosarcoma of the liver is extremely rare. Here, we report an unusual case of carcinosarcoma of the liver containing combined hepatocellular carcinoma and cholangiocarcinoma. A 66-year-old man with a history of viral hepatitis B was admitted for investigation of multiple liver masses. Dynamic computed tomography revealed a mostly hypoenhancing main tumor with a peripheral ring enhancement and several satellite nodules. After transcatheter arterial chemoembolization and portal vein embolization, an extended right posterior sectionectomy was performed. The resected tumor was macroscopically a simple nodular type, 4.3 × 4.2 cm in diameter, with a dense fibrous capsule. The pathological findings showed that both carcinomatous and sarcomatous elements were present, and diagnosis of carcinosarcoma of the liver was confirmed. The carcinomatous element consisted of hepatocellular carcinoma and cholangiocarcinoma. The sarcomatous element was composed of spindle cells. Immunohistochemical studies demonstrated that cytokeratin AE1/AE3, human serum albumin, cytokeratin 7, and Arginase-1 were partially positive in tumor cells of the carcinomatous element but not in tumor cells of the sarcomatous element. Follow-up for 30 months after surgery has shown no signs of recurrence.
Keyphrases
  • computed tomography
  • sars cov
  • magnetic resonance imaging
  • induced apoptosis
  • oxidative stress
  • cell proliferation
  • positron emission tomography
  • endoplasmic reticulum stress
  • nitric oxide synthase