Cronkhite-Canada Syndrome Successfully Treated by Corticosteroids before Presenting Typical Ectodermal Symptoms
نویسندگان
چکیده
منابع مشابه
Cronkhite-Canada syndrome presenting as eosinophilic gastroenteritis.
Cronkhite-Canada syndrome (CCS), first described in 1955, is a rare clinical syndrome of unknown etiology. CCS is diagnosed clinically, and the presenting symptoms include alopecia, cutaneous hyperpigmentation, gastrointestinal polyposis, and onychodystrophy, often accompanied by diarrhea, weight loss, and abdominal pain. We describe a unique case of CCS that presented with eosinophilic infiltr...
متن کاملCronkhite-Canada syndrome.
A 50-year-old woman suffered from anorexia, taste disturbance and a weight loss of 13 kg over a period of 6 months. Physical examination showed onychotrophia (Picture 1), skin pigmentation (Picture 2) and alopecia. Gastroscopy revealed multiple reddish sessile polyps in the antrum and anglus of the stomach (Picture 3). Colonoscopy revealed multiple reddish sessile polyps through the colon and i...
متن کاملCronkhite-Canada syndrome.
Cronkhite-Canada syndrome is one of the rare causes of multiple polyposis, characterised by generalised gastrointestinal polyposis, cutaneous hyperpigmentation, alopecia, and nail dystrophy.' Although Cronkhite and Canada described it for the first time in 1955, little is known about its aetiology and the prognosis remains poor. We describe a case of CronkhiteCanada syndrome in a 79-year-old Ja...
متن کاملThe Cronkhite-Canada syndrome
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. The jejunum, though macroscopically normal, showed oedema, increased vascularity and mucous gland secreting a...
متن کامل[The Cronkhite-Canada syndrome].
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. The jejunum, though macroscopically normal, showed oedema, increased vascularity and mucous gland secreting a...
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ژورنال
عنوان ژورنال: Case Reports in Gastroenterology
سال: 2020
ISSN: 1662-0631
DOI: 10.1159/000510920