Results 1 to 10 of about 17,887 (159)

Diffuse Symptomatic Familial Gastric Polyposis Requiring Total Gastrectomy: A Complex Case Report [PDF]

Reports
Background and Clinical Significance: Familial gastric polyposis is a rare condition associated with an increased risk of malignant transformation, particularly in patients with a strong family history of gastrointestinal malignancies. Case Presentation:
Ivan Pesic, Ilija Golubovic, Milorad Pavlovic, Milica Nestorovic, Ivan Ilic   +4 more
doaj   +2 more sources

Mapping Genetic Modifiers of Polyp Formation in Smad4-Deficient Juvenile Polyposis Using the Collaborative Cross Mouse Population [PDF]

Cells
Juvenile Polyposis Syndrome (JPS) is an autosomal dominant disorder characterized by multiple gastrointestinal polyps and an increased risk of cancer, most commonly associated with mutations in the tumor suppressor gene Smad4.
Osayd Zohud, Kreem Midlej, Iqbal M. Lone, Aysar Nashef, Imad Abu-Elnaaj, Fuad A. Iraqi   +5 more
doaj   +2 more sources

Familial pediatric Peutz–Jeghers syndrome with recurrent intussusception: case report and literature review [PDF]

Frontiers in Pediatrics
BackgroundPeutz–Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by mucocutaneous pigmentation and gastrointestinal hamartomatous polyposis, predisposing affected individuals to recurrent small bowel intussusception and ...
Sondes Sahli, Sondes Sahli, Bochra Aziza, Bochra Aziza, Nada Sghairoun, Nada Sghairoun, Asma Slimani, Asma Slimani, Nadia Boujelbene, Nadia Boujelbene, Nadia Boujelbene, Rim Missaoui, Rim Missaoui, Rim Missaoui, Zohra Rahal, Zohra Rahal, Said Jlidi, Said Jlidi   +17 more
doaj   +2 more sources

A Rare Cause of Intestinal Polyposis. [PDF]

Dtsch Arztebl Int, 2019
Keim VJ, Goßner L.
europepmc   +4 more sources

Schistosoma Mansoni and Haematobium: Radiological Diagnostic Clues and Pathophysiology [PDF]

Pathogens
Schistosomiasis (bilharzia) is a parasitic infection caused by trematodes of the Schistosoma genus and remains a significant health burden in endemic regions. Granulomatous host responses to deposited Schistosoma eggs in small veins and tissues result in
Sultan Abdulwadoud Alshoabi, Abdullatif O. Magram, Abdulaziz H. Alkalady, Rafat Rashed Al-Maqtari, Khaled M. Almas, Khaled Mohammed Al-Sayaghi, Abdullgabbar M. Hamid, Fahad H. Alhazmi, Abdulaziz A. Qurashi, Walaa Alsharif, Amirah Alsaedi, Ezzat AbuAzzah, Abdulkareem Algahtani, Khaled A. Alqfail, Khalid M. Alshamrani   +14 more
doaj   +2 more sources

AXIN2-Associated Adenomatous Colorectal Polyposis

Journal of Coloproctology, 2021
Introduction Most cases of colorectal cancer (CRC) occur sporadically; however, ∼ 3% to 6% of all CRCs are related to inherited syndromes, such as Lynch syndrome and familial adenomatous polyposis (FAP).
Bruno Augusto Alves Martins, Reinaldo Falluh Filho, Romulo Medeiros de Almeida, Renata Lazari Sandoval   +3 more
doaj   +1 more source

Familial adenomatous colorectal polyposis complicated by colonic obturation: a clinical case

Кубанский научный медицинский вестник, 2020
Background. Colorectal obturation is a fairly rare complication in patients with colorectal polyposis. Case descriptions of colonic obturation with underlying familial adenomatous colorectal polyposis have not been reported to date in national and ...
V. M. Durleshter, A. A. Kryachko, K. D. Chuguzov, M. K. Tarlanova   +3 more
doaj   +1 more source

ZnO nanoparticles promote the malignant transformation of colorectal epithelial cells in APCmin/+ mice

Environment International, 2022
As the use of zinc oxide nanoparticles (ZnO NPs) in everyday products grows, so does concern about health risks. However, no findings on the gastrointestinal toxicity of ZnO NPs have been published.
Jian Meng, Juan Yang, Ting Pan, Xianjun Qu, Shuxiang Cui   +4 more
doaj   +1 more source

Danish guidelines for management of non-APC-associated hereditary polyposis syndromes

Hereditary Cancer in Clinical Practice, 2021
Hereditary Polyposis Syndromes are a group of rare, inherited syndromes characterized by the presence of histopathologically specific or numerous intestinal polyps and an increased risk of cancer. Some polyposis syndromes have been known for decades, but
Anne Marie Jelsig, John Gásdal Karstensen, Niels Jespersen, Zohreh Ketabi, Charlotte Lautrup, Karina Rønlund, Lone Sunde, Karin Wadt, Ole Thorlacius-Ussing, Niels Qvist   +9 more
doaj   +1 more source

Familial Intestinal Polyposis [PDF]

Journal of Clinical Pathology, 1947
The articles published by the Annals of Eugenics (1925–1954) have been made available online as an historical archive intended for scholarly use. The work of eugenicists was often pervaded by prejudice against racial, ethnic and disabled groups. The online publication of this material for scholarly research purposes is not an endorsement of those views
openaire   +5 more sources