Hereditary Cancer Syndromes—A Primer on Diagnosis and Management, Part 2

Gastrointestinal Cancer Syndromes

Niloy Jewel Samadder, Noemi Baffy, Karthik Giridhar, Fergus J Couch, Douglas Riegert-Johnson

Research output: Contribution to journalReview article

1 Citation (Scopus)

Abstract

Hereditary causes due to mutations and defects in certain genes account for roughly 5% to 10% of all colorectal cancers. These inherited syndromes have been associated with a 60% to 100% lifetime risk for development of colorectal cancer, depending on the genetic syndrome, and many also carry an increased risk for multiple extracolonic malignancies. In this second part of a review series on hereditary cancer syndromes, the focus will be to provide guidance on the features and management of the most commonly encountered hereditary colorectal cancers and polyposis conditions including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, and hamartomatous polyposis.

Original languageEnglish (US)
Pages (from-to)1099-1116
Number of pages18
JournalMayo Clinic proceedings
Volume94
Issue number6
DOIs
StatePublished - Jun 1 2019

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Gastrointestinal Neoplasms
Colorectal Neoplasms
Hereditary Neoplastic Syndromes
Hereditary Nonpolyposis Colorectal Neoplasms
Neoplasms
Adenomatous Polyposis Coli
Mutation
Genes

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Hereditary Cancer Syndromes—A Primer on Diagnosis and Management, Part 2 : Gastrointestinal Cancer Syndromes. / Samadder, Niloy Jewel; Baffy, Noemi; Giridhar, Karthik; Couch, Fergus J; Riegert-Johnson, Douglas.

In: Mayo Clinic proceedings, Vol. 94, No. 6, 01.06.2019, p. 1099-1116.

Research output: Contribution to journalReview article

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