摘要
报告1例Cronkhite-Canada综合征。患者男,36岁。味觉减退、腹泻1个月余,面部、四肢末端皮肤变黑20d,脱发10d入院。皮肤科检查:面部、四肢末端色素沉着,指(趾)甲变薄脆裂,普秃。内镜检查发现全肠道息肉。出院2个月后症状自行缓解。1年后因肠道息肉增大行右半结肠切除术。
A case of Cronkhite-Canada syndrome was reported. A 36-year-old man presented with hypogeusia and diarrhea for 1 month, and skin hyperpigmenation and alopecia subsequently developed. Physical examination showed hyperpigmenation of his face and extremities, nail dystrophy and alopecia universalis. Endoscope revealed multiple polyps in the whole gastrointestinal tract. The patient experienced spontaneous remission after 2 months. One year later right hemicolectomy was operated due to enlargement of polyps.
出处
《临床皮肤科杂志》
CAS
CSCD
北大核心
2008年第5期293-296,共4页
Journal of Clinical Dermatology