Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 1
1969 2
1972 1
1973 3
1974 1
1975 2
1976 1
1978 3
1981 1
1983 2
1984 1
1985 1
1987 4
1988 1
1989 3
1990 3
1991 1
1992 4
1993 4
1994 9
1995 8
1996 3
1997 5
1998 5
1999 10
2000 6
2001 5
2002 4
2003 1
2004 5
2005 11
2006 8
2007 5
2008 7
2009 7
2010 4
2011 10
2012 8
2013 4
2014 6
2015 8
2016 7
2017 5
2018 5
2019 5
2020 3
2021 9
2022 8
2023 8
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

216 results

Results by year

Filters applied: . Clear all
Page 1
Peutz-Jeghers syndrome.
Tacheci I, Kopacova M, Bures J. Tacheci I, et al. Curr Opin Gastroenterol. 2021 May 1;37(3):245-254. doi: 10.1097/MOG.0000000000000718. Curr Opin Gastroenterol. 2021. PMID: 33591027 Review.
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kinase B1 (STK11/LKB1) genes. …
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartoma …
Pathology and genetics of hereditary colorectal cancer.
Ma H, Brosens LAA, Offerhaus GJA, Giardiello FM, de Leng WWJ, Montgomery EA. Ma H, et al. Pathology. 2018 Jan;50(1):49-59. doi: 10.1016/j.pathol.2017.09.004. Epub 2017 Nov 21. Pathology. 2018. PMID: 29169633 Review.
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, Peutz-Jeghers syndrome, juvenile polyposis and Cowden/PTEN hamartoma syndrome. In addition, serrated polyposis is a clinical …
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated po …
DICER1 tumor predisposition syndrome: an evolving story initiated with the pleuropulmonary blastoma.
González IA, Stewart DR, Schultz KAP, Field AP, Hill DA, Dehner LP. González IA, et al. Mod Pathol. 2022 Jan;35(1):4-22. doi: 10.1038/s41379-021-00905-8. Epub 2021 Oct 1. Mod Pathol. 2022. PMID: 34599283 Free PMC article. Review.
The detection of the germline mutation in DICER1 provided the opportunity to identify and continue to recognize a number seemingly unrelated extrapulmonary neoplasms: Sertoli-Leydig cell tumor, gynandroblastoma, embryonal rhabdomyosarcomas of the cervix and other sites, multinodu …
The detection of the germline mutation in DICER1 provided the opportunity to identify and continue to recognize a number seemingly unrelated …
DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies.
Schultz KAP, Williams GM, Kamihara J, Stewart DR, Harris AK, Bauer AJ, Turner J, Shah R, Schneider K, Schneider KW, Carr AG, Harney LA, Baldinger S, Frazier AL, Orbach D, Schneider DT, Malkin D, Dehner LP, Messinger YH, Hill DA. Schultz KAP, et al. Clin Cancer Res. 2018 May 15;24(10):2251-2261. doi: 10.1158/1078-0432.CCR-17-3089. Epub 2018 Jan 17. Clin Cancer Res. 2018. PMID: 29343557 Free PMC article. Review.
In addition to conferring increased cancer risks for pleuropulmonary blastoma (PPB) and ovarian sex cord-stromal tumors, particularly Sertoli-Leydig cell tumor, individuals with pathogenic germline DICER1 variants may also develop lung cysts, cystic nephroma, renal sarcoma and Wi …
In addition to conferring increased cancer risks for pleuropulmonary blastoma (PPB) and ovarian sex cord-stromal tumors, particularly Sertol …
Clinical Guidelines for Diagnosis and Management of Peutz-Jeghers Syndrome in Children and Adults.
Yamamoto H, Sakamoto H, Kumagai H, Abe T, Ishiguro S, Uchida K, Kawasaki Y, Saida Y, Sano Y, Takeuchi Y, Tajika M, Nakajima T, Banno K, Funasaka Y, Hori S, Yamaguchi T, Yoshida T, Ishikawa H, Iwama T, Okazaki Y, Saito Y, Matsuura N, Mutoh M, Tomita N, Akiyama T, Yamamoto T, Ishida H, Nakayama Y. Yamamoto H, et al. Digestion. 2023;104(5):335-347. doi: 10.1159/000529799. Epub 2023 Apr 13. Digestion. 2023. PMID: 37054692 Free article. Review.
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis throughout the gastrointestinal tract, except for the esophagus, along with characteristic mucocutaneous pigmentation. ...Some patients with PJS develop gast …
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis throughout the ga …
Pathology of Gastrointestinal Polyposis Disorders.
Rosty C, Brosens LAA. Rosty C, et al. Gastroenterol Clin North Am. 2024 Mar;53(1):179-200. doi: 10.1016/j.gtc.2023.09.006. Epub 2023 Oct 20. Gastroenterol Clin North Am. 2024. PMID: 38280747 Review.
Gastrointestinal polyposis disorders are a group of syndromes defined by clinicopathologic features that include the predominant histologic type of colorectal polyp and specific inherited gene mutations. Adenomatous polyposis syndromes comprise the prototypical familial ad …
Gastrointestinal polyposis disorders are a group of syndromes defined by clinicopathologic features that include the predominant histologic …
Hamartomatous polyps: Diagnosis, surveillance, and management.
Gorji L, Albrecht P. Gorji L, et al. World J Gastroenterol. 2023 Feb 28;29(8):1304-1314. doi: 10.3748/wjg.v29.i8.1304. World J Gastroenterol. 2023. PMID: 36925460 Free PMC article. Review.
Hereditary polyposis syndrome can be divided into three categories: Ade-nomatous, serrated, and hamartomatous polyps. Hamartomatous polyps, malformations of normal tissue presenting in a disorganized manner, are characterized by an autosomal dominant i …
Hereditary polyposis syndrome can be divided into three categories: Ade-nomatous, serrated, and hamartomatous polyps. Hamar …
Hamartomatous Polyp of the Palatine Tonsil: A Case Report and Critical Literature Review.
do Amaral-Silva GK, Ribeiro-Brizola J, Santos ÁA, Cieslak-Sanches SR, Chicrala GM, Gaetti-Jardim EC, Antunes DM. do Amaral-Silva GK, et al. Head Neck Pathol. 2023 Jun;17(2):502-508. doi: 10.1007/s12105-023-01529-x. Epub 2023 Feb 1. Head Neck Pathol. 2023. PMID: 36723854 Free PMC article. Review.
BACKGROUND: Hamartomatous polyp of the palatine tonsil is a rare benign tumor poorly recognized by clinicians and pathologists. ...An excisional biopsy was performed under local anesthesia, and the microscopic aspect confirmed the diagnosis of the hamartomatous …
BACKGROUND: Hamartomatous polyp of the palatine tonsil is a rare benign tumor poorly recognized by clinicians and pathologists …
[Gastrointestinal polyposis syndromes].
Spier I, Hüneburg R, Aretz S. Spier I, et al. Internist (Berl). 2021 Feb;62(2):133-144. doi: 10.1007/s00108-020-00903-z. Internist (Berl). 2021. PMID: 33237439 Review. German.
OBJECTIVES: The present article aims to provide an overview of the differential diagnosis of different gastrointestinal polyposis syndromes based on the endoscopic findings, polyp histology, extraintestinal phenotype and molecular genetic diagnostics. ...RESULTS: In additi …
OBJECTIVES: The present article aims to provide an overview of the differential diagnosis of different gastrointestinal polyposis syndromes …
Evaluation and management of gastric epithelial polyps.
Castro R, Pimentel-Nunes P, Dinis-Ribeiro M. Castro R, et al. Best Pract Res Clin Gastroenterol. 2017 Aug;31(4):381-387. doi: 10.1016/j.bpg.2017.06.001. Epub 2017 Jun 13. Best Pract Res Clin Gastroenterol. 2017. PMID: 28842047 Review.
Gastric polyps include a wide spectrum of lesions with different histology and neoplastic potential. ...Polyposis syndromes that affect the stomach are rare but should be taken into account. Hamartomatous polyps can be found in Juvenile polyposis, Cowden synd …
Gastric polyps include a wide spectrum of lesions with different histology and neoplastic potential. ...Polyposis syndromes that affe …
216 results