摘要
Cronkhite-Canada综合征(Cronkhite-Canadasyndrome,CCS)非常罕见,病因不明,以胃肠道多发性息肉和外胚层三联征两大症候群为主,主要表现为慢性腹泻、腹部不适、毛发脱落、色素沉着、指(趾)甲萎缩等.本文报道CCS1例,通过病史及内镜检查结果并结合相关文献对该病进行分析讨论,探讨CCS的临床特征,提高对该病的认识.
Cronkhite-Canada syndrome （CCS） is a rare clinical entity of unknown etiology. It represents a syndrome of gastrointestinal polyposis associated with ectodermal changes, mainly manifesting as chronic diarrhea, abdominal discomfort, alopecia, skin hyperpigmentation, and nail dystrophy. Here, we present a case of CCS, describe the clinical and endoscopic findings, analyze the clinical features of the disease, and review the relevant literature.
出处
《世界华人消化杂志》
CAS
北大核心
2010年第9期958-960,共3页
World Chinese Journal of Digestology
