Literature DB >> 20567567

Hereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood.

Michael Manfredi1.   

Abstract

Hamartomatous polyposis syndromes are a rare group of hereditary autosomal dominant disorders that comprise less than 1% of all hereditary colorectal cancers. Hamartomatous polyps, in and of themselves, are benign entities; however, these hamartomatous polyposis syndromes have a malignant potential for the development of colorectal cancer as well as extracolonic cancers. Early detection and proper surveillance are vital to minimizing the risk of carcinoma. This article provides a critical review of the clinical presentation, pathology, genetics, and screening and surveillance guidelines of juvenile polyposis syndrome, PTEN hamartoma tumor syndrome, and Peutz-Jeghers syndrome.

Entities:  

Keywords:  Hamartomatous polyposis syndromes; PTEN hamartoma tumor syndrome; Peutz-Jeghers syndrome; juvenile polyposis syndrome

Year:  2010        PMID: 20567567      PMCID: PMC2886463     

Source DB:  PubMed          Journal:  Gastroenterol Hepatol (N Y)        ISSN: 1554-7914


  118 in total

1.  Peutz-Jeghers syndrome.

Authors:  J KYLE
Journal:  Scott Med J       Date:  1961-08       Impact factor: 0.729

Review 2.  PTEN function in normal and neoplastic growth.

Authors:  Lionel M L Chow; Suzanne J Baker
Journal:  Cancer Lett       Date:  2006-01-18       Impact factor: 8.679

Review 3.  Peutz-Jeghers syndrome: risks of a hereditary condition.

Authors:  A M Westerman; J H Wilson
Journal:  Scand J Gastroenterol Suppl       Date:  1999

4.  PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

Authors:  D J Marsh; J B Kum; K L Lunetta; M J Bennett; R J Gorlin; S F Ahmed; J Bodurtha; C Crowe; M A Curtis; M Dasouki; T Dunn; H Feit; M T Geraghty; J M Graham; S V Hodgson; A Hunter; B R Korf; D Manchester; S Miesfeldt; V A Murday; K L Nathanson; M Parisi; B Pober; C Romano; C Eng
Journal:  Hum Mol Genet       Date:  1999-08       Impact factor: 6.150

5.  Gastrointestinal hamartomatous polyposis in Lkb1 heterozygous knockout mice.

Authors:  Hiroyuki Miyoshi; Masayuki Nakau; Tomo-o Ishikawa; Michael F Seldin; Masanobu Oshima; Makoto M Taketo
Journal:  Cancer Res       Date:  2002-04-15       Impact factor: 12.701

Review 6.  LKB1, the multitasking tumour suppressor kinase.

Authors:  P A Marignani
Journal:  J Clin Pathol       Date:  2005-01       Impact factor: 3.411

Review 7.  Highly penetrant hereditary cancer syndromes.

Authors:  Rebecca Nagy; Kevin Sweet; Charis Eng
Journal:  Oncogene       Date:  2004-08-23       Impact factor: 9.867

8.  GI polyposis and glycogenic acanthosis of the esophagus associated with PTEN mutation positive Cowden syndrome in the absence of cutaneous manifestations.

Authors:  Thomas J McGarrity; Maria J Wagner Baker; Francesca M Ruggiero; Diane M Thiboutot; Heather Hampel; Xiao-Ping Zhou; Charis Eng
Journal:  Am J Gastroenterol       Date:  2003-06       Impact factor: 10.864

9.  Peutz-Jeghers syndrome in children: report of two cases and review of the literature.

Authors:  J A Tovar; I Eizaguirre; A Albert; J Jimenez
Journal:  J Pediatr Surg       Date:  1983-02       Impact factor: 2.545

10.  Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome.

Authors:  M G Dunlop
Journal:  Gut       Date:  2002-10       Impact factor: 23.059

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  20 in total

1.  Giant stomach secondary to juvenile polyposis syndrome.

Authors:  Nathalie Wong-Chong; Wondwossen Hailu Kidanewold; Richard Kirsch; Gary Robert May; Judith Andrea McCart
Journal:  J Gastrointest Surg       Date:  2011-10-18       Impact factor: 3.452

2.  BMPR1A mutation-positive juvenile polyposis syndrome and atrial septal defect: coincidence or association?

Authors:  Rachel E Harris; Richard K Russell
Journal:  BMJ Case Rep       Date:  2019-06-21

3.  Overlap of Juvenile polyposis syndrome and Cowden syndrome due to de novo chromosome 10 deletion involving BMPR1A and PTEN: implications for treatment and surveillance.

Authors:  Adebisi Alimi; Lauren A Weeth-Feinstein; Amy Stettner; Freddy Caldera; Jennifer M Weiss
Journal:  Am J Med Genet A       Date:  2015-04-05       Impact factor: 2.802

Review 4.  Small bowel polyposis syndromes.

Authors:  Nadir Arber; Menachem Moshkowitz
Journal:  Curr Gastroenterol Rep       Date:  2011-10

5.  Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation.

Authors:  Frank Schwenter; Marie E Faughnan; Abigail B Gradinger; Terri Berk; Robert Gryfe; Aaron Pollett; Zane Cohen; Steven Gallinger; Carol Durno
Journal:  J Gastroenterol       Date:  2012-02-14       Impact factor: 7.527

Review 6.  A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.

Authors:  Sarah Scollon; Amanda Knoth Anglin; Martha Thomas; Joyce T Turner; Kami Wolfe Schneider
Journal:  J Genet Couns       Date:  2017-03-29       Impact factor: 2.537

Review 7.  The biological complexity of colorectal cancer: insights into biomarkers for early detection and personalized care.

Authors:  Marina De Rosa; Daniela Rega; Valeria Costabile; Francesca Duraturo; Antonello Niglio; Paola Izzo; Ugo Pace; Paolo Delrio
Journal:  Therap Adv Gastroenterol       Date:  2016-08-07       Impact factor: 4.409

8.  Autosomal Dominant Inherited Cowden's Disease in a Family.

Authors:  Jun-Wook Ha
Journal:  Clin Endosc       Date:  2013-01-31

Review 9.  Hamartomatous Tumors in the Gastrointestinal Tract.

Authors:  Estell Cauchin; Yan Touchefeu; Tamar Matysiak-Budnik
Journal:  Gastrointest Tumors       Date:  2015-08-06

10.  Hamartomatous polyposis syndromes.

Authors:  Zoran Stojcev; Pawel Borun; Jacek Hermann; Piotr Krokowicz; Wojciech Cichy; Lukasz Kubaszewski; Tomasz Banasiewicz; Andrzej Plawski
Journal:  Hered Cancer Clin Pract       Date:  2013-06-01       Impact factor: 2.857

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