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Squamous cell carcinoma of liver and intrahepatic biliary tract is an extremely rare, primary, malignant liver and biliray tract epithelial tumor originating in the intrahepatic bile duct epithelium histologically characterized by the presence of keratinization and/or intracellular bridges. Patients typically present abdominal pain in the right upper quadrant, jaundice, nausea, vomiting, anorexia, weight loss, fever and/or dyspepsia.
Biomarker and diagnostic research for squamous cell carcinoma of liver and intrahepatic biliary tract has been reported in the published literature.
No clinical trials have been registered for squamous cell carcinoma of liver and intrahepatic biliary tract.
5 publications have been identified in PubMed for squamous cell carcinoma of liver and intrahepatic biliary tract. Research spans Case Report / Case Series (60%), Diagnostic / Biomarker (20%), and Review / Meta-Analysis (20%).
Rikitake R (2025). [PMID: 40376725](https://pubmed.ncbi.nlm.nih.gov/40376725/). *Pathology international*. [Review / Meta-Analysis]
Benhamdane A (2024). [PMID: 38984177](https://pubmed.ncbi.nlm.nih.gov/38984177/). *European journal of case reports in internal medicine*. [Case Report / Case Series]
Pulappadi VP (2024). [PMID: 39822406](https://pubmed.ncbi.nlm.nih.gov/39822406/). *Cureus*. [Case Report / Case Series]
Gerber TS (2024). [PMID: 38212892](https://pubmed.ncbi.nlm.nih.gov/38212892/). *International journal of cancer*. [Diagnostic / Biomarker]
Ma QJ (2024). [PMID: 39071465](https://pubmed.ncbi.nlm.nih.gov/39071465/). *World journal of clinical oncology*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 21, 2026, 12:28 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center