Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper

Translated title of the contribution: New hereditary polyposis syndromes in the patient with intestinal polyps

Anne Marie Jelsig*, Niels Jespersen, John Gásdal Karstensen, Zohreh Ketabi, Karina Rønlund, Lone Sund, Ole Thorlacius-Ussing, Karin Wadt, Niels Qvist, Charlotte Kvist Lautrup

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

Hereditary polyposis syndromes (HPS) are a group of rare, inherited syndromes characterised by the presence of histopathological specific or numerous intestinal polyps and a high risk of intestinal and extraintestinal cancer. During the last decade, several new HPS have been discovered, as it is possible to detect pathogenic germline variants in genes not previously known to be associated with polyposis. This review summarises the current knowledge on the syndromes and discusses genetic testing as part of the diagnostic pipeline when suspecting a polyposis syndrome.
Translated title of the contributionNew hereditary polyposis syndromes in the patient with intestinal polyps
Original languageDanish
Article numberV02210148
JournalUgeskrift for Læger
Volume2022
Issue number6
ISSN0041-5782
Publication statusPublished - 2022

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