空肠血管瘤并发肠套叠甚为罕见,现将我院1例报道如下。 女性,40岁,因腹痛、腹胀、呕吐和停止排便排气3天,于1984年2月22日入院。外院诊断为急性肠梗阻,经输液和抗感染治疗无效转我院。近5年来患者经常腹部不适,均按溃疡病治疗,效果不明显。 体检:全身残表淋巴结不肿大,心肺正常。腹部略膨隆,腹软,未见肠型.上腹及脐周有压痛,无明显肿物们及,肠鸣音亢进。肛门指诊阴性。腹部平片上可见散在的小液平面数个。入院诊断为急性肠梗阻。经保守治疗不见好转。于同月28日行剖腹 Intussusception with jejunal hemangiomas is very rare. One case in our hospital is now reported as follows. The woman, 40 years old, was admitted to the hospital on February 22, 1984 for three days due to abdominal pain, bloating, vomiting, and stop of defecation. The diagnosis of acute intestinal obstruction in the outer hospital was ineffective after transfusion and anti-infective treatment. In the past 5 years, patients often have abdominal discomfort. All patients are treated with ulcer disease. The effect is not obvious. Physical examination: The residual lymph nodes of the body are not swollen and the heart and lungs are normal. The abdomen was slightly bulging and soft in the abdomen. There was no bowel type. There was tenderness on the upper abdomen and umbilical cord. There were no obvious masses and bowel sounds. Anal test was negative. A few small liquid planes scattered on the abdominal plain film. The admission diagnosis was acute intestinal obstruction. Conservative treatment did not improve. On the 28th of the same month, laparotomy