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Cronkhite-Canada 증후군 1예
A Case of Cronkhite-Canada Syndrome
정성태, 정의창, 최지호, 성경제, 문기찬, 고재경 (Sung Tae Chung, Eul Chang Chung, Jee Ho Choi, Kyung Jeh Sung, Kee Chan Moon and Jai Kyoung Koh)
UCI I410-ECN-0102-2009-510-005412823

The Cronkhite-Canada syndrome is a rare, non-neoplastic, non-hereditary condition which consists of gastrointestinal polyposis associated with alopecia, onychodystrophy and hyperpigmentation of the skin. It usually encountered with severe diarrhea, weight loss and other malabsorption symptoms. The etiology of the condition is unknown. Usually, this syndrome is associated with a poor prognosis due to the effect of malabsorption and generalized debility. We report a case of this syndrome showing unusually rapid improvement after 3-month following only conservative treatment. To our knowledge, this is the first case report of Cronkhite-Canada syndrome in the Karean dermatologic literature. (Korean J Dermatol 1999;37(3): 381-385)

[자료제공 : 네이버학술정보]
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