Results 11 to 20 of about 460 (115)

Clinical and Endoscopic Response to Anti-Tumor Necrosis Factor-Alpha Antibody Therapy in a Patient With Cronkhite-Canada Syndrome [PDF]

Journal of Investigative Medicine High Impact Case Reports, 2023
Cronkhite-Canada syndrome (CCS) is an acquired polyposis syndrome with gastrointestinal and extraintestinal manifestations. Given its rarity and lack of standard treatment, diagnosis and treatment are challenging.
Roham Salman Roghani, Joline De Castro, Adewale B. Ajumobi   +2 more
doaj   +2 more sources

Infliximab treatment for Cronkhite-Canada syndrome in pregnancy: A case report [PDF]

Case Reports in Women's Health
Cronkhite-Canada syndrome (CCS) is a rare nonhereditary disorder characterized by gastrointestinal polyps and protein-losing enteropathy. While an increasing number of CCS cases have been reported worldwide, no documented cases involving pregnant ...
Ayano Rosemary Nakamura, Shuji Yamamoto, Yoshitsugu Chigusa, Masaki Mandai, Haruta Mogami   +4 more
doaj   +2 more sources

Case Report: A case of Cronkhite-Canada syndrome associated with sigmoid colon cancer and early esophageal cancer [PDF]

Frontiers in Medicine
This article reports a case of a patient with Cronkhite-Canada syndrome combined with sigmoid colon cancer and early esophageal cancer. In this case, CCS was diagnosed simultaneously with the discovery of sigmoid colon cancer and early esophageal cancer.
Yumeng Wang, Yumeng Wang, Wenyan Sun, Wenyan Sun, Dingxin Wang, Conghui Cai, Qicheng Fan, Zhihang Huang, Yun Bai   +8 more
doaj   +2 more sources

Deep vein thrombosis in a patient with Cronkhite-Canada syndrome: a complex case report [PDF]

Thrombosis Journal, 2023
Background Cronkhite-Canada syndrome (CCS) is a rare disease characterized by generalized gastrointestinal polyps, ectodermal abnormalities and variable gastrointestinal symptoms.
Xiao-Kai Feng, Xiao-Fen Chen, Bei-Bei Wang, Zhi-Gang Zeng, Chao Liu, Wei-Hong Sha, Juan Ma   +6 more
doaj   +2 more sources

Cronkhite‒Canada syndrome as inflammatory hamartomatous polyposis: new evidence from whole transcriptome sequencing of colonic polyps [PDF]

Orphanet Journal of Rare Diseases
Background Cronkhite-Canada syndrome (CCS) is a rare, nonhereditary disease characterized by diffuse gastrointestinal polyposis and ectodermal abnormalities.
Shuang Liu, Yunfei Zhi, Runfeng Zhang, Yan You, Wen You, Qiushi Xu, Jingnan Li, Ji Li   +7 more
doaj   +2 more sources

Hair Loss and Polyposis in Cronkhite-Canada Syndrome [PDF]

Gastro Hep Advances, 2022
Kenji Yamazaki, Hiroyuki Sato, Masahito Shimizu   +2 more
doaj   +2 more sources

Cronkhite-Canada Syndrome: A rare Case Report from Nepal

Journal of Nepal Health Research Council, 2021
Cronkhite-Canada syndrome first described in 1955, is a rare clinical syndrome of unknown etiology. Since then, more than 500 cases have been reported worldwide in the literature.
Nitesh R. Pokharel, Prajwol Shrestha, Vivek Sharma, Sumit Pandey   +3 more
doaj   +1 more source

Cronkhite-Canada Syndrome Associated With Superficial Esophageal Carcinoma: A Case Report and Literature Review

Frontiers in Medicine, 2022
IntroductionCronkhite-Canada syndrome is a rare disease characterized by generalized gastrointestinal polyposis, alopecia, skin pigmentation, and onychotrophia with no generally recognized mechanism of pathogenesis.
Yan Zhao, Fujing Lv, Xun Yang, Yongjun Wang, Shutian Zhang, Peng Li   +5 more
doaj   +1 more source

Cronkhite-Canada syndrome: An atypical presentation with subungual hyperkeratosis [PDF]

JAAD Case Reports
Peerada Sermswan, MD, Pravit Asawanonda, MD, DSc, Nopadon Noppakun, MD, Chanat Kumtornrut, MD, MSc   +3 more
doaj   +2 more sources

Early feeding reduces length of hospital stay in patients with acute lower gastrointestinal bleeding: A large multicentre cohort study

Colorectal Disease, Volume 25, Issue 11, Page 2206-2216, November 2023., 2023
Abstract Aim No studies have compared the clinical outcomes of early and delayed feeding in patients with acute lower gastrointestinal bleeding (ALGIB). This study aimed to evaluate the benefits and risks of early feeding in a nationwide cohort of patients with ALGIB in whom haemostasis was achieved.
Takaaki Kishino, Tomonori Aoki, Eiji Sadashima, Katsumasa Kobayashi, Atsushi Yamauchi, Atsuo Yamada, Jun Omori, Takashi Ikeya, Taiki Aoyama, Naoyuki Tominaga, Yoshinori Sato, Naoki Ishii, Tsunaki Sawada, Masaki Murata, Akinari Takao, Kazuhiro Mizukami, Ken Kinjo, Shunji Fujimori, Takahiro Uotani, Minoru Fujita, Hiroki Sato, Sho Suzuki, Toshiaki Narasaka, Junnosuke Hayasaka, Tomohiro Funabiki, Yuzuru Kinjo, Akira Mizuki, Shu Kiyotoki, Tatsuya Mikami, Ryosuke Gushima, Hiroyuki Fujii, Yuta Fuyuno, Naohiko Gunji, Yosuke Toya, Kazuyuki Narimatsu, Noriaki Manabe, Koji Nagaike, Tetsu Kinjo, Yorinobu Sumida, Sadahiro Funakoshi, Kiyonori Kobayashi, Tamotsu Matsuhashi, Yuga Komaki, Mitsuru Kaise, Naoyoshi Nagata   +44 more
wiley   +1 more source