ArticleHereditary cancer in clinical practice2013
Hamartomatous polyposis syndromes.
Article in Hereditary cancer in clinical practice, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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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.
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Who cites it
12 citing papers in PubMed, 24 citations in OpenAlex.
- SMAD4 variants and its genotype-phenotype correlations to juvenile polyposis syndrome.Hereditary cancer in clinical practice · 2023Review
- PTEN and LKB1 are differentially required in Gli1-expressing mesenchymal cells to suppress gastrointestinal polyposis.Cell reports · 2022Article
- Peutz-Jeghers Syndrome Manifested as Multiple Polyps in Jejunum With Intussusception.Journal of medical cases · 2022Article
- Clinical and Histologic Overlap and Distinction Among Various Hamartomatous Polyposis Syndromes.Clinical and translational gastroenterology · 2019Article
- Colorectal carcinoma in the course of inflammatory bowel diseases.Hereditary cancer in clinical practice · 2019Review
- Correlation between genotype and phenotype in three families with Peutz-Jeghers Syndrome.Experimental and therapeutic medicine · 2017Article
- Giant rectal polyp prolapse in an adult patient with the Peutz-Jeghers syndrome.BMJ case reports · 2016Article
- Magnifying chromoendoscopic and endocytoscopic findings of juvenile polyps in the colon and rectum.Oncology letters · 2016Article
- Carcinosarcoma with Choriocarcinomatous and Osteosarcomatous Differentiation in a Patient with Juvenile Polyposis Syndrome.Rare tumors · 2015Article
- Colorectal cancer risk in hamartomatous polyposis syndromes.World journal of gastrointestinal surgery · 2015Review
- Colorectal polyps and polyposis syndromes.Gastroenterology report · 2014Article
- A giant rectal villous adenoma with a malicious intent.Gastrointestinal cancer research : GCR · 2013Article
Corrections and comments
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Authors and funding
8 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hamartomas are tumour-like malformations, consisting of disorganized normal tissues, typical of the site of tumour manifestation. Familial manifestation of hamartomatous polyps can be noted in juvenile polyposis syndrome (JPS), Peutz-Jeghers' syndrome (PJS), hereditary mixed polyposis syndrome (HMPS) and PTEN hamartoma tumour syndrome (PHTS). All the aforementioned syndromes are inherited in an autosomal dominant manner and form a rather heterogenous group both in respect to the number and localization of polyps and the risk of cancer development in the alimentary tract and other organs. Individual syndromes of hamartomatous polyposis frequently manifest similar symptoms, particularly during the early stage of the diseases when in several cases their clinical pictures do not allow for differential diagnosis. The correct diagnosis of the disease using molecular methods allows treatment to be implemented earlier and therefore more effectively since it is followed by a strict monitoring of organs that manifest a predisposition for neoplastic transformation.
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.