The Landmark Series: Hilar Cholangiocarcinoma. Review uri icon

Overview

abstract

  • Hilar cholangiocarcinoma (HC) is a rare and highly aggressive biliary tract neoplasm. As such, the data driving the management of this disease generally are not based on prospective clinical trial data but rather consist of retrospective experiences and limited level 1 data. Surgical resection offers the best chance of a long-term survival, but local and distant recurrences are common. This report presents landmark articles that form the basis of preoperative, operative, and adjuvant strategies for HC.

publication date

  • April 7, 2021

Research

keywords

  • Bile Duct Neoplasms
  • Cholangiocarcinoma
  • Klatskin Tumor

Identity

PubMed Central ID

  • PMC9273057

Scopus Document Identifier

  • 85103927590

Digital Object Identifier (DOI)

  • 10.1245/s10434-021-09871-6

PubMed ID

  • 33829358

Additional Document Info

volume

  • 28

issue

  • 8