| Literature DB >> 34216004 |
Takashi Ofuchi1, Katsunori Imai2, Yosuke Nakao1, Shigeki Nakagawa1, Yuta Shiraishi1, Rikako Kato1, Rumi Itoyama1, Toshihiko Yusa1, Takaaki Higashi1, Hiromitsu Hayashi1, Tsuguharu Asato3, Yo-Ichi Yamashita1, Yoshiki Mikami3, Hideo Baba1.
Abstract
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.Entities:
Keywords: Carcinosarcoma; Combined hepatocellular carcinoma and cholangiocarcinoma; Liver
Year: 2021 PMID: 34216004 DOI: 10.1007/s12328-021-01469-5
Source DB: PubMed Journal: Clin J Gastroenterol ISSN: 1865-7265