Gastrointestinal Polyposes and Lynch Syndrome - a Pathologists Perspective
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
31409084
DOI
10.14735/amko2019s92
PII: 113307
Knihovny.cz E-zdroje
- Klíčová slova
- Lynch syndrome, colorectal carcinoma, gastrointestinal polyposes,
- MeSH
- dědičné nádorové syndromy * diagnóza genetika patologie MeSH
- gastrointestinální nádory * diagnóza genetika patologie MeSH
- lidé MeSH
- mutace MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Gastrointestinal polyposes and Lynch syndrome are a group of heterogenous hereditary tumor syndromes associated with an increased risk of developing colorectal carcinoma and other malignancies. Typical early manifestations of gastrointestinal polyposes include multiple polyps in the gastrointestinal tract. Early recognition of these syndromes enables patients carrying a pathogenic mutation to undergo screening and to instigate precautions to minimize the risk of developing tumors. In some cases, gastrointestinal lesions could be an early indicator of tumor syndrome and histopathologic examination could lead to a recommendation for genetic testing of patients and their families. Supported by Ministry of Health, Czech Republic - Conceptual Development of Research Organization (MMCI, 00209805). The authors declare they have no potential conflicts of interest concerning drugs, products,or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers. Submitted: 16. 4. 2019 Accepted: 6. 6. 2019.
Citace poskytuje Crossref.org