克朗凯特-加拿大综合征

Med J Aust. 1976 Mar 13;1(11):347-8.

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.

本文描述了澳大利亚首例罕见的克朗凯特-加拿大综合征，该综合征包括全身性胃肠道息肉病、脱发、甲萎缩和色素沉着。患者最初因甲状腺功能减退接受治疗，但随后发展为蛋白丢失性肠病和息肉内发生的结肠癌。