| Literature DB >> 33829358 |
Kevin C Soares1,2, William R Jarnagin3,4.
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.Entities:
Mesh:
Year: 2021 PMID: 33829358 PMCID: PMC9273057 DOI: 10.1245/s10434-021-09871-6
Source DB: PubMed Journal: Ann Surg Oncol ISSN: 1068-9265 Impact factor: 4.339