A Case of Cronkhite-Canada Syndrome Showing Spontaneous Remission
Intestinal Research
; : 317-322, 2013.
Article
in Ko
| WPRIM
| ID: wpr-55521
Responsible library:
WPRO
ABSTRACT
Cronkhite-Canada syndrome (CCS) is a rare, noninherited gastrointestinal polyposis syndrome associated with ectodermal changes such as alopecia, nail dystrophy, and cutaneous hyperpigmentation. The etiology and pathogenesis of CCS are not known, but diarrhea, malnutrition, gastrointestinal bleeding, and infection may occur in the affected patient; moreover, this condition could be fatal. However, previous reports have described several cases of spontaneous remission. We report a 60-year-old man who was incidentally found to have colonic polyposis, alopecia, and hypogeusia and was diagnosed to have CCS. However, this patient experienced spontaneous remission, including regrowth of body hair and alleviation of bowel inflammation, without any specific medications such as steroids, antibiotics, or proton pump inhibitors.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Remission, Spontaneous
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Steroids
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Hyperpigmentation
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Colon
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Ageusia
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Intestinal Polyposis
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Malnutrition
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Diarrhea
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Ectoderm
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Alopecia
Limits:
Humans
Language:
Ko
Journal:
Intestinal Research
Year:
2013
Type:
Article