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

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

Clinical journal of gastroenterology - 1 Oct 2020

Ohwada Sae, Yamashita Kentaro, Kazama Tomoe, Mitsuhashi Kei, Ichiyanagi Akiko, Nakachi Kohei, Yamano Hiro-O, Nobuoka Takayuki, Ito Tatsuya, Sasao Wataru, Nakase Hiroshi

Abstract excerpt

A female patient in her 80s was referred to our hospital because of an ileal tumor identified by capsule endoscopy. FDG-PET suggested double intestinal tumors not only in the ileum but also in the jejunum. The patient has cancer past history including sigmoid colon, rectum, and endometrium, and also had cancer family history fulfilling the revised Amsterdam criteria. Double balloon enteroscopy disclosed two...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Colorectal Neoplasms, Hereditary Nonpolyposis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA-Binding Proteins

Share to Germ Cells

Share to Germ-Line Mutation

Share to Mutation

Source

Identifiers

PMID: 32519314
DOI: 10.1007/s12328-020-01147-y

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Double small bowel cancers leading to the diagnosis of Lynch syndrome with germline MSH6 mutation in an elderly patient.PMID 32519314Read ↗

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

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

Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing.Semantic proximity Read ↗

Early detection of duodenal cancer by upper gastrointestinal-endoscopy in Lynch syndrome.Semantic proximity Read ↗

Thirty-nine-year-old with familial colon cancer, and variant of undetermined significance in MSH6.Semantic proximity Read ↗

Attenuated adenomatous polyposis with MSH6 variation: two case reportsSemantic proximity Read ↗

Small intestinal adenocarcinoma accompanied by lynch syndrome: A case report.Semantic proximity Read ↗

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancerSemantic proximity Read ↗

Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome.Semantic proximity Read ↗

Meta-analysis of MSH6 gene mutation frequency in colorectal and endometrial cancers.Semantic proximity Read ↗

High risk of multiple gastric cancers in Japanese individuals with Lynch syndromeSemantic proximity Read ↗

Small bowel carcinoma revealing HNPCC syndrome.Semantic proximity Read ↗

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