ReviewThe Surgical clinics of North America2008
Hamartomatous polyposis syndromes.
Review in The Surgical clinics of North America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 2 of them syntheses that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
44 citing papers in PubMed, 2 syntheses or guidelines pooled it, 137 citations in OpenAlex.
- A systematic review of symptomatic hamartomas of the jejunum and ileum.Annals of the Royal College of Surgeons of England · 2022Pooled it
- ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.The American journal of gastroenterology · 2015Guideline
- Juvenile Polyposis Syndrome in a Post-Fontan Adolescent With Tetralogy of Fallot: A Rare Association With Important Cancer Risk and Developmental Overlap.ACG case reports journal · 2026Article
- Narrow-band imaging with magnification for the diagnosis of colorectal adenoma in a patient with Cronkhite-Canada syndrome.DEN open · 2024Article
- SMAD4 variants and its genotype-phenotype correlations to juvenile polyposis syndrome.Hereditary cancer in clinical practice · 2023Review
- A case report of Cronkhite-Canada syndrome first encounterd at a hospital in northern Vietnam.Annals of medicine and surgery (2012) · 2023Article
- Solitary Peutz-Jeghers Type Hamartomatous Polyp Arising from the Appendix.GE Portuguese journal of gastroenterology · 2023Article
- A NewDiagnostics (Basel, Switzerland) · 2022Article
- Peutz-Jeghers Syndrome and the Role of Imaging: Pathophysiology, Diagnosis, and Associated Cancers.Cancers · 2021Review
- Article
- [Weight loss, diarrhea and dystrophic alterations of the fingernails in an 80-year-old male patient].Der Internist · 2021Article
- Cronkhite-Canada Syndrome Associated with Gastric Outlet Obstruction and Membranous Nephropathy: A Case Report and Review of the Literature.Internal medicine (Tokyo, Japan) · 2020Review
- Small bowel polyp resection using device-assisted enteroscopy in Peutz-Jeghers Syndrome: Results of a specialised tertiary care centre.United European gastroenterology journal · 2020Observational
- Epidemiology of colorectal cancer: incidence, mortality, survival, and risk factors.Przeglad gastroenterologiczny · 2019Review
- Differential diagnosis of solitary gastric Peutz-Jeghers-type polyp with stomach cancer: a case report.International journal of surgery case reports · 2018Article
- Cronkhite-Canada syndrome associated with colon cancer metastatic to liver: A case report.Medicine · 2017Article
- Peutz-Jeghers syndrome with intermittent upper intestinal obstruction: A case report and review of the literature.Medicine · 2017Review
- Familial Colorectal Cancer: Understanding the Alphabet Soup.Clinics in colon and rectal surgery · 2016Review
- Extra-ampullary Peutz-Jeghers polyp causing duodenal intussusception leading to biliary obstruction: a case report.Journal of medical case reports · 2016Article
- Endoscopic and clinical evaluation of treatment and prognosis of Cronkhite-Canada syndrome: a Japanese nationwide survey.Journal of gastroenterology · 2016Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
Since the histologic description of the hamartomatous polyp in 1957 by Horrilleno and colleagues, descriptions have appeared of several different syndromes with the propensity to develop these polyps in the upper and lower gastrointestinal tracts. These syndromes include juvenile polyposis, Peutz-Jeghers syndrome, hereditary mixed polyposis syndrome, and the phosphatase and tensin homolog gene (PTEN) hamartoma tumor syndromes (Cowden and Bannayan-Riley-Ruvalcaba syndromes), which are autosomal-dominantly inherited, and Cronkhite-Canada syndrome, which is acquired. This article reviews the clinical aspects, the molecular pathogenesis, the affected organ systems, the risks of cancer, and the management of these hamartomatous polyposis syndromes. Although the incidence of these syndromes is low, it is important for clinicians to recognize these disorders to prevent morbidity and mortality in these patients, and to perform presymptomatic testing in patients at risk.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.