Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Synchronous adenocarcinoma of the endometrium and colon in a woman with Lynch syndrome associated with a mutation of the MSH6 gene.

Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia - 1 Jan 2025

Valencia Cardona Andrés Felipe, Cruz Barbosa Jhoan Sebastián, Cortés Buelvas Armando

Abstract excerpt

INTRODUCTION: Lynch syndrome (LS) is an autosomal dominant genetic condition, accounting for an estimated prevalence of 2-3% of the causes of hereditary colorectal carcinoma. In addition, it increases the risk of endometrial and ovarian cancer, among others. CASE REPORT: A 56-year-old woman with a 6-month history of pelvic pain, dyspareunia and hypermenorrhoea. Family history: her mother died of endometrial...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenocarcinoma
Share to Carcinoma, Endometrioid

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Colonic Neoplasms

Share to Colorectal Neoplasms, Hereditary Nonpolyposis

Share to DNA-Binding Proteins

Share to Endometrial Neoplasms

Share to Mutation

Share to Neoplasms, Multiple Primary

Source

Identifiers

PMID: 40215653
DOI: 10.1016/j.patol.2025.100826

Genes

MSH6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Synchronous adenocarcinoma of the endometrium and colon in a woman with Lynch syndrome associated with a mutation of the MSH6 gene.PMID 40215653Read ↗

Endometrial and ovarian cancer in women with Lynch syndrome: update in screening and prevention.Semantic proximity Read ↗

Risks of Lynch Syndrome Cancers for MSH6 Mutation CarriersSemantic proximity Read ↗

Colorectal cancer in Lynch syndrome associated with PMS2 and MSH6 mutations.Semantic proximity Read ↗

Double small bowel cancers leading to the diagnosis of Lynch syndrome with germline MSH6 mutation in an elderly patient.Semantic proximity Read ↗

Recently identified colon cancer predispositions: MYH and MSH6 mutations.Semantic proximity Read ↗

MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancerSemantic proximity Read ↗

Coexisting germline variants of MLH1 and MSH6 in a patient with Lynch syndrome, endometrial cancer, and ovarian cancerSemantic proximity Read ↗

Prospective Determination of Prevalence of Lynch Syndrome in Young Women With Endometrial CancerSemantic proximity Read ↗

Associations Between Mutations in MSH6 and PMS2 and Risk of Surveillance-detected Colorectal Cancer.Semantic proximity Read ↗

Lynch syndrome type II associated endometrial carcinoma: a case report and literature analysisSemantic proximity Read ↗

An unusual tumor spectrum in Lynch syndrome caused by MSH6 mutationSemantic proximity Read ↗

A Unique Case of Rectal Cancer with Coexistence of Multiple Pathways of CarcinogenesisSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.