Results 1 to 10 of about 18,555 (114)

Familial Adenomatous Polyposis: A Case Report [PDF]

The Annals of African Surgery
Familial adenomatous polyposis (FAP) is a rare disease syndrome characterized by mutations in the Adenomatous Polyposis Coli gene. Affected people have a markedly increased lifetime risk of colorectal cancer. The patient was a 17-year-old female with a 4-
Francois Adrien Bokalli, Carelle Njembele Koum, Willy Nyaga, Peninah Nthambi, Mark Tharao, Dan Kiptoon   +5 more
doaj   +3 more sources

Clinical impact of hospital distance and center transfers on adherence and outcomes in familial adenomatous polyposis: A multicenter retrospective study in a defined region of Japan. [PDF]

PLoS ONE
This study aimed to evaluate how hospital distance and changes in surveillance hospitals influence adherence to surveillance, the cumulative risk of familial adenomatous polyposis-related tumors, and survival outcomes in patients with familial ...
Kyota Tatsuta, Mayu Sakata, Moriya Iwaizumi, Kazuya Okamoto, Shigeto Yoshii, Yutaro Asaba, Takashi Harada, Kiyotaka Kurachi, Mikihiro Shimizu, Hiroya Takeuchi   +9 more
doaj   +2 more sources

Worldwide Impact of Upper Gastrointestinal Disease in Familial Adenomatous Polyposis [PDF]

Diagnostics
Familial adenomatous polyposis (FAP) is the most common hereditary colorectal adenomatous polyposis and cancer syndrome which has historically been associated with a near absolute risk of colorectal cancer.
Mahnur Haider, Muaaz Masood, Bryson W. Katona, Carol A. Burke, Gautam N. Mankaney   +4 more
doaj   +2 more sources

Morphological Analyses of Colorectal Adenocarcinomas in Japanese Familial Adenomatous Polyposis Patients

Journal of the Anus, Rectum and Colon, 2022
Objectives: This retrospective study was conducted to clarify the morphological characteristics of colorectal cancer (CRC) in Japanese familial adenomatous polyposis (FAP) patients.
Yozo Suzuki, Fumio Ishida, Hideyuki Ishida, Hideki Ueno, Hirotoshi Kobayashi, Tatsuro Yamaguchi, Tsuyoshi Konishi, Yukihide Kanemitsu, Takao Hinoi, Yasuhiro Inoue, Naohiro Tomita, Kenichi Sugihara   +11 more
doaj   +1 more source

Mutation Spectrum of Familial Adenomatous Polyposis Patients in Turkish Population: Identification of 3 Novel APC Mutations

The Turkish Journal of Gastroenterology, 2022
Background: Familial adenomatous polyposis (OMIM #175100) and MUTYH-associated polyposis (OMIM #608456) are rare cancerprone disorders characterized by hundreds of adenomatous polyps in the colon and rectum, which have a high probability of malignant ...
Esra Arslan Ateş, Ceren Alavanda, Şenol Demir, Çağlayan Keklikkıran, Wafi Attaallah, Osman Cavit Özdoğan, Ahmet İlter Güney   +6 more
doaj   +1 more source

Current clinical practice for familial adenomatous polyposis in Japan: A nationwide multicenter study

Annals of Gastroenterological Surgery, 2022
Introduction In Japanese patients with familial adenomatous polyposis (FAP), colectomy tends to be postponed or avoided. Aim This study aimed to clarify the current clinical practice from a Japanese multicenter cohort study database.
Takaaki Matsubara, Naohito Beppu, Masataka Ikeda, Hideyuki Ishida, Yoji Takeuchi, Toshiya Nagasaki, Akinari Takao, Kazuhito Sasaki, Kiwamu Akagi, Tomoya Sudo, Hideki Ueno, Tatsuro Yamaguchi, Naohiro Tomita, Yoichi Ajioka   +13 more
doaj   +1 more source

Risk of extracolonic malignancies and metachronous rectal cancer after colectomy and ileorectal anastomosis in familial adenomatous polyposis

Asian Journal of Surgery, 2022
Background: Analysis of long-term clinical outcomes of patients with familial adenomatous polyposis is critical in reducing or preventing the incidence of extracolonic malignancies after initial surgery.
Kazuhito Sasaki, Hiroaki Nozawa, Kazushige Kawai, Koji Murono, Shigenobu Emoto, Junko Kishikawa, Hiroaki Ishii, Yuichiro Yokoyama, Shinya Abe, Yuzo Nagai, Hiroyuki Anzai, Hirofumi Sonoda, Tetsuro Taira, Soichiro Ishihara   +13 more
doaj   +1 more source

Large Rearrangements in Genes Responsible for Familial Adenomatous Polyposis, MUTYH-Associated Polyposis and Peutz–Jeghers Syndrome in Russian Patients

Российский журнал гастроэнтерологии, гепатологии, колопроктологии, 2023
Аim: to reveal the rate of large rearrangements in the genes responsible for familial adenomatous polyposis, MUTYH-associated polyposis and Peutz–Jeghers syndrome.Materials and methods. The MLPA method was used for identification of large rearrangements.
A. N. Loginova, Yu. A. Shelygin, V. P. Shubin, A. M. Kuzminov, D. Yu. Pikunov, T. A. Saveleva, A. S. Tsukanov   +6 more
doaj   +1 more source

Vaccines for cancer interception in familial adenomatous polyposis [PDF]

Frontiers in Immunology
Mary L Disis, Disis Mary L
exaly   +2 more sources

Serrated Polyposis Syndrome: A Literature Review

Journal of Coloproctology, 2023
Serrated polyposis syndrome is considered the most prevalent colonic polyposis syndrome in the world. Its importance has been increasingly discussed due to the significant increase in the risk of developing colorectal cancer in its affected individuals ...
Guilherme Campos Stephanini, Nathan Assis Jordão Pinto, Jarbas Faraco, Paulo Alberto Falco Pires Correa   +3 more
doaj   +1 more source