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本科1985～1988年收治黑斑息肉病(Peutz Jeghers综合征)5例,现报道如下。临床资料男3例,女2例,年龄18～46岁。5例均有唇、口腔粘膜、指、趾色素沉着,4例有家族史。因腹痛、间断性便血或血便就诊。4例并发肠套叠。1例左下腹肿块伴部分肠梗阻。经纤维内窥镜和气钡双重造影等检查,发现息肉分布于胃、小肠和结肠等处。小肠息肉个数最多。1例行左半结肠和部分空、回肠切除;2例作直肠息肉圈套器套扎和电灼切除;作肠粘连松解术和剖
In 1985-1988, five cases of Peetz Jeghers syndrome were treated in the undergraduate program. The report is as follows. Clinical data were 3 males and 2 females, aged 18 to 46 years. All 5 cases had pigmentation of the lips, oral mucosa, fingers and toes, and 4 cases had a family history. Treated with abdominal pain, intermittent blood or bloody stools. Intussusception was complicated in 4 cases. 1 case of left lower abdominal mass with partial intestinal obstruction. Through fiberoptic endoscopy and airway double contrast examination, it was found that polyps were distributed in the stomach, small intestine and colon. The largest number of small intestine polyps. 1 case of left colon and partial empty and ileum resection; 2 cases of rectal polyps snare and electrocautery resection; as intestinal adhesion and lysis