| Literature DB >> 15768184 |
Kuo-Chih Tseng1, Bor-Shyang Sheu, Jenq-Chang Lee, Hong-Ming Tsai, Nan-Tsing Chiu, Yuan-Chang Dai.
Abstract
Cronkhite-Canada syndrome is a rare form of nonhereditary gastrointestinal polyposis associated with ectodermal change and protein-losing enteropathy. Here we report a 63-year-old male presenting with diffuse gastrointestinal polyposis, onychodystrophy, cutaneous pigmentation, alopecia, diarrhea, hypoalbuminemia and lower leg edema. Technetium-99m-labeled human serum albumin scan confirmed the patient to have protein-losing enteropathy, which originated from the transverse and descending colon. Subtotal colectomy was performed. Albumin level and ectodermal change were gradually improved during three years of outpatient clinic follow-up. Based on our finding, Technetium-99m-labeled human serum albumin scintigraphy is helpful to localize the protein-losing origins and surgery is an effective treatment for Cronkhite-Canada syndrome with protein-losing enteropathy.Entities:
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Year: 2005 PMID: 15768184 DOI: 10.1007/s10350-004-0836-0
Source DB: PubMed Journal: Dis Colon Rectum ISSN: 0012-3706 Impact factor: 4.585