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遗传性皮肤粘膜色素斑—胃肠息肉综合征为1921年 Peutz 首先报道,1949年 Jeghers 详细描述,故又称 Peutz-Jeghers 综合征(下称 PJS)。临床特点为皮肤特膜色素斑和胃肠道多发性息肉,是一种少见的遗传性疾病.本文报告1例 PJS,并综合国内文献作一复习.病例报告:丁某某,男,50岁,住院号171368.主诉头昏乏力15年,面色苍黄9个月,以“缺铁性贫血”于1986年4月21日收入院,患者自幼即被发现口唇有色素斑,以为是“胎记”未就诊.1950年因“肠套叠”在外院手术治疗.1962～1975年曾多次行鼻息肉摘除术.1971年因腹痛黑便在我院诊断为十二指球部溃疡并行胃大部切除术,术后仍时有腹痛.因常便血于1981年在外院行“外痔”切除
Hereditary mucocutaneous pigment spots - gastrointestinal polyps syndrome was first reported by Peutz in 1921, Jeghers in 1949 described in detail, it is also known as Peutz-Jeghers syndrome (hereinafter referred to as PJS). Clinical features of the skin melanoma and gastrointestinal polyp is a rare genetic disease.This article reports a case of PJS, and a comprehensive domestic literature for a review. Case report: Ding Moumou, male, 50 years old , Hospital number 171368. Chief complaint dizziness 15 years, pale yellow 9 months to “iron deficiency anemia” in April 21, 1986 income hospital, the patient was found that his lips pigmented, as “birthmark ”Unfilled .1950 due to“ intussusception ”in the outer hospital surgical treatment .1962 ~ 1975 had multiple nasal polyps removal. 1971 due to abdominal pain black in my hospital diagnosed as duodenal ulcer parallel gastric Department of resection, abdominal pain after surgery is still sometimes due to abnormal blood in the hospital in 1981, “External Hemorrhoids” resection