Cronkhite-Canada综合征1例

Cronkhite-Canada syndrome: A case report and review of the literature

Cronkhite-Canada综合征(Cronkhite-Canada’s syndrome, CCS)是临床罕见病,病因及发病机制尚不明确,该病以胃肠道多发息肉及外胚层两大症候群为主,临床表现以腹泻为主,全消化道多发息肉,伴有皮肤色素沉着、毛发脱落、指(趾)甲萎缩脱落等.预后较差,本文报道1例CCS患者并对62篇国内文献进行回顾性分析.

Cronkhite-Canada＇s syndrome（CCS） is a rare clinical entity of unknown etiology and has a poor prognosis. It is characterized by gastrointestinal polyposis with ectodermal changes. Main clinical manifestations include diarrhea and diffuse gastrointestinal polyposis, accompanied by skin pigmentation, alopecia, and nail changes. Here we report a case of CCS and performed a literature review.