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Cronkhite-Canada Syndrome: A Rare Cause of Gastrointestinal Polyposis With Response to Emerging Therapy. [PDF]
ACG Case Rep JKhadarian K, Pai R, Samadder NJ.
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Cronkhite-Canada syndrome with esophagus involvement and six-year follow-up: A case report. [PDF]
World J GastroenterolTang YC.
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Infantile Cronkhite-Canada syndrome
Indian Journal of Pediatrics, 1997Since 1955, numerous cases of Cronkhite-Canada syndrome have been reported in adults. We present here the first Asian report of the infantile Cronkhite-Canada syndrome. While the prognosis in adults is variable, in children, it is less optimistic.
D G, de Silva +4 more
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Pharmacological management of Cronkhite–Canada syndrome
Expert Opinion on Pharmacotherapy, 2003Cronkhite-Canada syndrome (CCS) is a rare, non-inherited gastrointestinal polyposis syndrome associated with characteristic ectodermal abnormalities. A number of potentially life-threatening complications including malnutrition, gastrointestinal bleeding and infection may occur in affected patients and CCS is fatal in many cases.
Eric M, Ward, Herbert C, Wolfsen
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Cronkhite-Canada Syndrome With Hypothyroidism
Southern Medical Journal, 2005Cronkhite-Canada syndrome is a rare, noninherited gastrointestinal polyposis syndrome associated with characteristic ectodermal abnormalities. This report describes a 60-year-old female who was diagnosed with Cronkhite-Canada syndrome with hypothyroidism after presenting with chronic diarrhea, alopecia, intermittent abdominal pain, generalized ...
Mei, Qiao +3 more
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Radiology, 1972
Wilma Canada Diner, M.D., wishes to correct a misquotation of the pathologist on whose findings the original report of the Cronkhite-Canada syndrome was based. The intestinal lesions usually have characteristics of cystically dilated hyperplastic glands and should be referred to as inflammatory pseudopolyps or cystic glandular dilatation rather than ...
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Wilma Canada Diner, M.D., wishes to correct a misquotation of the pathologist on whose findings the original report of the Cronkhite-Canada syndrome was based. The intestinal lesions usually have characteristics of cystically dilated hyperplastic glands and should be referred to as inflammatory pseudopolyps or cystic glandular dilatation rather than ...
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Medical Journal of Australia, 1962
The first case in Australia of the rare Cronkhite-Canada syndrome which comprises generalized gastrointestinal polyposis, alopecia, onychatrophia and pigmentation, is described. The patient was initially treated for hypothyroidism, but subsequently developed protein-losing enteropathy and adenocarcinoma of the colon arising in the polyp.
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The first case in Australia of the rare Cronkhite-Canada syndrome which comprises generalized gastrointestinal polyposis, alopecia, onychatrophia and pigmentation, is described. The patient was initially treated for hypothyroidism, but subsequently developed protein-losing enteropathy and adenocarcinoma of the colon arising in the polyp.
openaire +2 more sources