Results 21 to 30 of about 510 (145)

Cronkhite-Canada Syndrome: A rare Case Report from Nepal

open access: yesJournal 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   +3 more
doaj   +1 more source

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

open access: yesFrontiers 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   +5 more
doaj   +1 more source

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

open access: yesJAAD Case Reports
Peerada Sermswan, MD   +3 more
doaj   +2 more sources

The Cronkhite-Canada syndrome [PDF]

open access: yesPostgraduate Medical Journal, 1973
Summary The eighteenth patient and seventh survivor with the Cronkhite-Canada syndrome is described. A remission of 9 years followed gastrectomy and steroid therapy. Findings on seventeen other patients described in the literature are reviewed. The histological features are discussed in detail.
J A, Cotterill   +4 more
openaire   +2 more sources

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

open access: yesColorectal 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   +44 more
wiley   +1 more source

Cronkhite–Canada syndrome: report of a rare case and review of the literature

open access: yesJournal of International Medical Research, 2020
Cronkhite–Canada syndrome is rarely encountered in clinical practice. Notably, most patients with Cronkhite–Canada syndrome exhibit hypoalbuminemia.
Yuping Liu   +3 more
doaj   +1 more source

Cancer risk and mortality in patients with solitary juvenile polyps—A nationwide cohort study with matched controls

open access: yesUnited European Gastroenterology Journal, Volume 11, Issue 8, Page 745-749, October 2023., 2023
Abstract Introduction The risk of cancer in patients with solitary colorectal juvenile polyps (JPs) is poorly investigated and several studies have reported polyps with dysplastic and adenomatous alterations. We aimed to investigate the long‐term risk of cancer and mortality in these patients by merging data from national registers and comparing them ...
Anne Marie Jelsig   +5 more
wiley   +1 more source

Multicenter propensity score‐matched analysis comparing short versus long cap‐assisted colonoscopy for acute hematochezia

open access: yesJGH Open, Volume 7, Issue 7, Page 487-496, July 2023., 2023
While short and long attachment caps are available for colonoscopy, it is unclear which type is more appropriate for acute hematochezia. This study has shown that long cap‐assisted colonoscopy is superior to short cap colonoscopy for the diagnosis of acute hematochezia, particularly colonic diverticular bleeding, and the detection of active bleeding ...
Mariko Kobayashi   +45 more
wiley   +1 more source

Cronkhite-Canada Syndrome: Report of Three Cases and Literature Review [PDF]

open access: yesZhongguo quanke yixue, 2022
Cronkhite-Canada syndrome (CCS) is currently considered to be a non-genetic disorder and a relatively rare clinical condition that is characterized endoscopically by multiple polyps in the gastrointestinal tract and clinically manifested by ...
LI Shuying, LIN Yingmin, WANG Min
doaj   +1 more source

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