摘要
目的记录并报道Cronkhite—Canada综合征1例,以加强对本病的认识。方法搜集患者的临床资料,包括症状、体征及辅助检查,查阅相关文献,尝试各种治疗方法。结果患者符合Crankhite—Canada综合征,普通的中西止泻药物无效,激素治疗有效。结论Cronkhite—Canada综合征患者为非家族性,镜下特点为多发胃肠道息肉,以腹泻为主要症状并伴有外胚层改变。普通止泻药物无效,可尝试激素治疗。
Objective To improve the recognition of Cronkhite-Canada syndrome (CCS) by reporting a case. Methods Collect the data of the patient,including the clinical feature, sign and the labo- ratory examination, review the related literatures, and try several therapies. Results The patient was con- sistant with CCS, and no ordinary antidiarrhea drugs but glucocorticosteroids are effective. Conclusions CCS is a rare non-familial syndrome, which is characterized by diffuse gastrointestinal polyposis, dystrophic changes of the fingernails, alopecia, cutaneous hyperpigmentation and diarrhea, commom antidiarrhea drugs is ineffective. ,and man can try glucocorticosteroids therapy.
出处
《临床内科杂志》
CAS
2010年第4期255-257,共3页
Journal of Clinical Internal Medicine