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机构地区:[1]广东省惠州市惠阳三和医院消化内科,广东惠州516211 [2]广东省惠州市东江病理中心,广东惠州516001
出 处:《罕少疾病杂志》2014年第5期38-40,F0003,共4页Journal of Rare and Uncommon Diseases
摘 要:目的提高对Peutz—Jeghers综合征的认识。方法对我院诊断的3例P-J综合征的临床资料进行回顾性分析。结果 3例均发现黑色素斑,胃肠镜示胃及大肠多发息肉3例,胶囊内镜示胃及小肠多发息肉1例,1例有家族聚集现象,3例行内镜下治疗效果良好。结论 P-J综合征根据特殊部位黑色素斑沉着,结合胃肠镜检查,尽早确诊,内镜下治疗并加强随访是目前最好的治疗方法。Objective To raise the awareness of Peutz-Jeghers syndrome.Methods The data of 3 patients confirmed with Peutz-Jeghers syndrome in our hospital were retrospectively studied.Results The melanocytic macule deposition were showed in 3 patients, and gastrointestinal endoscopy showed gastric and large intestine polyps in 3 patients. Capsule endoscopy showed stomach and small intestine polyps in 1 casew, and 1 case showed family aggregation. 3 cases showed curative effect under endoscopic therapy.Conclusion Peutz-Jeghers syndrome should be early diagnosed according to special-site pigmentation combined with gastrointestinal endoscopy examination. Endoscopic therapy and follow-up is the best treatment to patients with Peutz-Jeghers Syndrome at present.
分 类 号:R322.44[医药卫生—人体解剖和组织胚胎学]
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