Literature DB >> 30244221

Intrahepatic sarcomatoid cholangiocarcinoma.

Sara Sintra1, Rui Costa2, Carlos Filipe1, Adélia Simão1.   

Abstract

Sarcomatoid carcinoma is a rare tumour composed of intermingled malignant epithelial and mesenchymal cells, and it has been reported in various organs including the liver. Sarcomatoid cholangiocarcinoma (CCC) is an extremely rare liver primary tumour. Here, we report a case of an elderly man who was admitted to our hospital after head trauma. He performed a head CT that diagnosed cerebral metastasis. On abdominal CT, he presented a 10×8×9 cm-sized hypodense liver mass in the VII and VIII segments, with peripheral enhancement. Histological and immunohistochemical examination of the tumour showed a malignant neoplasm with both carcinomatous and sarcomatous components and positive expression of cytokeratin and vimentin antibodies. The patient was diagnosed with intrahepatic sarcomatoid CCC at an advanced stage and died 45 days after the diagnosis. We emphasise the importance of immunohistochemistry which may provide a clue to proper diagnosis. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  hepatic cancer; liver disease

Mesh:

Year:  2018        PMID: 30244221     DOI: 10.1136/bcr-2018-225017

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  2 in total

Review 1.  Sarcomatoid intrahepatic cholangiocarcinoma in a patient with poor prognosis: a case report and literature review.

Authors:  Xu Li; Jian Li; Kai Liu; Ludong Tan; Yahui Liu
Journal:  J Int Med Res       Date:  2020-11       Impact factor: 1.671

2.  Intrahepatic sarcomatoid cholangiocarcinoma: A case report of the youngest patient on record and a review of the condition's characteristics.

Authors:  Long-Fu Xi; Yun Jin; Jiang-Tao Li
Journal:  Front Surg       Date:  2022-09-01
  2 in total

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