Results 31 to 40 of about 460 (115)
The Diagnosis of Cronkhite-Canada Syndrome with CT Enterography: A Clinical Case Analysis
CT Lilun yu yingyong yanjiu, 2023 Cronkhite-Canada syndrome (CCS) is a rare cause of chronic diarrhea and malabsorption where patients develop multiple polyps throughout the gastrointestinal (GI) tract, accompanied by ectodermal changes.
Xuesong ZHAO +6 more
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Cronkhite-Canada Syndrome (CCS)—A Rare Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2015 Cronkhite-Canada syndrome (CCS) is an extremely rare non-inherited condition characterized by gastrointestinal hamartomatous polyposis, alopecia, onychodystrophy, hyperpigmentation, weight loss and diarrhoea.
SUBRATA CHAKRABARTI
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Cronkhite-Canada Syndrome Associated with Metastatic Colon Cancer
Case Reports in Gastroenterology, 2018 Cronkhite-Canada syndrome is characterized by gastrointestinal and ectodermal manifestations. In this paper, we describe a 64-year-old Iranian male, presenting with Cronkhite-Canada syndrome with metastatic colon cancer.
Shirin Haghighi +2 more
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Sirolimus in Refractory Cronkhite-Canada Syndrome and Focus on Standard Treatment
Journal of Investigative Medicine High Impact Case Reports, 2018 Cronkhite-Canada syndrome is a rare syndrome consisting of extensive gastrointestinal polyposis and ectodermal changes including cutaneous hyperpigmentation, alopecia, and onychodystrophy.
Catherine Langevin MD +4 more
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Cronkhite-Canada syndrome: case description
Italian Journal of Medicine, 2014 We present the case of an 80-year old woman affected by the Cronkhite-Canada syndrome. This rare disease was described for the first time in 1955. It is characterized by the growth of multiple polyps in the gastroenteric tract, leading to diarrhea ...
Andrea Da Porto +4 more
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A Misdiagnosed Case of Hypertrophic Gastropathy
Case Reports in Pathology, Volume 2020, Issue 1, 2020., 2020 Hypertrophic gastropathy is a rare idiopathic hyperproliferative disorder which may present as Menetrier’s disease (MD) characterized by foveolar hyperplasia in the gastric fundus and body. It is often accompanied by a severe loss of plasma proteins (including albumin) from the altered gastric mucosa.
Sushma Thapa +5 more
wiley +1 more source
Cronkhite-Canada Syndrome: Gastric Involvement Diagnosed by MDCT
Case Reports in Medicine, 2009 Chronkhite-Canada is a rare nonfamilial polyposis syndrome that usually presents as chronic malabsorption in adults. We present a case of a-73-year old woman with chronic gastrointestinal bleeding and malnutrition.
Jonathan D. Samet +3 more
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Case Reports in Pediatrics, Volume 2020, Issue 1, 2020., 2020 Laugier–Hunziker syndrome is a rare, acquired disorder characterized by mucocutaneous hyperpigmentation and melanonychia striata with no underlying systemic abnormalities. We report an 8‐year‐old boy with Laugier–Hunziker syndrome who presented with melanonychia striata affecting all the fingernails and toenails, macular pigmentation on the tongue and ...
Alexander K. C. Leung +4 more
wiley +1 more source
Steroid responsive mononeuritis multiplex in the Cronkhite-Canada syndrome
Frontiers in Neurology, 2016 The Cronkhite-Canada syndrome (CCS) is a rare disorder of unknown origin characterized by generalized gastrointestinal polyposis, alopecia, hyperpigmentation and onychodystrophy.
YL Lo, KH Lim, XM Cheng, S Mesenas
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Clinical and Radiological Features of Cronkhite–Canada Syndrome: A Case Report
Journal of Gastrointestinal and Abdominal Radiology, 2022 Cronkhite–Canada syndrome is a rare non-hereditary disease characterized by gastrointestinal hamartomatous polyposis and protein-losing enteropathy.
Lokesh Lokesh +5 more
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