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Article

Lynch syndrome-associated colorectal cancer in a 16-year-old girl due to a de novo MSH2 mutation.

BMJ case reports - 1 Jul 2020

Zajo Kristin, Colace Susan I, Mouhlas Danielle, Erdman Steven H

Abstract excerpt

The diagnosis of paediatric colorectal cancer is an unusual finding often diagnosed at an advanced stage with associated poor survival. Paediatric colorectal cancer warrants investigation for hereditary cancer predisposition syndromes, including Lynch syndrome. Here we describe a 16-year-old girl who presented with a stage IIA mucinous adenocarcinoma of the descending colon (T3 N0 M0) treated by resection alone...

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Share to Adenocarcinoma, Mucinous
Share to Colonoscopy
Share to Colorectal Neoplasms, Hereditary Nonpolyposis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Germ-Line Mutation

Share to MutS Homolog 2 Protein

Share to Tomography, X-Ray Computed

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Source

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Identifiers

PMID: 32611652
DOI: 10.1136/bcr-2019-233935
PMCID: PMC7332177

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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