Results 1 to 10 of about 32,367 (234)

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

Poliposis linfomatosa intestinal Intestinal lymphomatous polyposis

Medisan, 2009
Se expone el caso clínico de un paciente de 55 años de edad, de piel blanca, que acudió a la consulta de Gastroenterología por presentar diarreas desde hacía alrededor de un año, dolor abdominal difuso, pérdida de peso, astenia y anorexia.
Cesar Falagán Andina, Elba Patricia Cabezas Niubó, Inocente Rodríguez Reyes, Lilibet Zamora Cabezas, Jesús Fernández Duharte   +4 more
doaj   +3 more sources

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

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

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

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 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

Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis

Frontiers in Immunology, 2018
Cap polyposis is a rare gastrointestinal disease characterized by multiple inflammatory polyps located between the distal colon and the rectum. Despite the lack of clarity regarding its pathogenesis, mucosal prolapse, chronic inflammatory responses, and ...
Kazuki Okamoto, Tomohiro Watanabe, Yoriaki Komeda, Ayana Okamoto, Kosuke Minaga, Ken Kamata, Kentaro Yamao, Mamoru Takenaka, Satoru Hagiwara, Toshiharu Sakurai, Tomonori Tanaka, Hiroki Sakamoto, Kiyoshige Fujimoto, Naoshi Nishida, Masatoshi Kudo   +14 more
doaj   +1 more source

Acute WNT signalling activation perturbs differentiation within the adult stomach and rapidly leads to tumour formation [PDF]

, 2013
A role for WNT signalling in gastric carcinogenesis has been suggested due to two major observations. First, patients with germline mutations in adenomatous polyposis coli (APC) are susceptible to stomach polyps and second, in gastric cancer, WNT ...
A Gregorieff, A Horii, A Jung, A Novak, AC de Vries, AN Milne, AT Franco, B Kim, B Tycko, C Cavard, D Athineos, D M Pritchard, DM Parkin, E Half, E Tahara, EF Chan, G Gatta, H Guillen-Ahlers, H Ireland, H Luche, H Nagase, H Oshima, H Shibata, H Watanabe, H Zhang, HC Zheng, HJ Freeman, J Cordero, J Neumann, J Parsonnet, J Woodgett, JG Forte, K Miyazawa, K Oien, KF Becker, KW Kinzler, LK Bianchi, M Crabtree, M Iida, M Nakayama, M Shitashige, M Suzuki, M Suzuki, M Torbenson, MG Smith, MP Ebert, N Barker, N Barker, N Barker, N Barker, N Barker, N Harada, N Murata-Kamiya, N Uemura, O J Sansom, O Sokolova, O Tetsu, OJ Sansom, P Blache, P Correa, P Correa, P Lauren, P Salgueiro, P Soriano, PJ Guilford, R A Ridgway, R Kemp, R Poulsom, S Garrean, S Nakatsuru, S Patel, S Patel, S Radulescu, S Segditsas, S Sekine, SC Abraham, SC Abraham, SM Przemeck, SS Ng, T Gnad, T Oda, TC He, WM Clements, WS Park, XC He, Y Miyoshi, Y Park do, Z Spicer, Z Zhao   +88 more
core   +1 more source

Polyposis deserves a perfect physical examination for final diagnosis: Bannayan-Riley-Ruvalcaba syndrome

The Turkish Journal of Pediatrics, 2017
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare autosomal dominant inherited polyposis syndrome characterized by macrocephaly, lipomatosis, hemangiomatosis, intestinal polyposis and pigmented macules on penis.
Hayriye Hızarcıoğlu-Gülşen, Esra Kılıç, Elena Dominguez-Garrido, Yusuf Aydemir, Gülen Eda Utine, İnci Nur Saltık-Temizel   +5 more
doaj   +1 more source