Sakai Takehiro, Sato Koichi, Sudo Yasuhiro, Koyanagi Masashi, Hasegawa Yoshie, Hiraga Noriko, Sawaya Manabu, Tohno Hiroshi, Tanaka Masanori
Department of Surgery, Hirosaki City Hospital, 3-8-1 O-machi, Hirosaki, Aomori 036-8004, Japan.
Surg Today. 2006;36(12):1118-21. doi: 10.1007/s00595-006-3305-7. Epub 2006 Dec 25.
An 18-year-old man was admitted to a local hospital with abdominal pain and bloody stool. Upper and lower gastrointestinal endoscopy failed to show any bleeding sites; however, an angiography of the superior mesenteric artery done on hospital day 4 showed an abnormal artery with an aneurysm, branching from the ileal artery. This artery was thought to be the vitellointestinal artery, a feeding artery of Meckel diverticulum. After embolization, he was transferred to our hospital, where we performed emergency laparotomy with partial resection of the ileum, including a bleeding Meckel diverticulum. Pathological examination revealed ectopic gastric mucosa and peptic ulceration, which we assumed was the origin of the bleeding. The patient had an uneventful postoperative course. Visceral artery aneurysms are rare but important vascular lesions because of their potential for fatal rupture. Although a minimally invasive procedure can be performed for a vitellointestinal artery aneurysm in patients with asymptomatic Meckel diverticulum, we treated our patient surgically because he presented with hemorrhagic shock and had been unresponsive to an H(2)-receptor antagonist.
一名18岁男性因腹痛和便血入住当地医院。上下消化道内镜检查未发现任何出血部位;然而,入院第4天进行的肠系膜上动脉血管造影显示,有一条异常动脉,带有一个动脉瘤,从回肠动脉分支出来。这条动脉被认为是卵黄肠管动脉,即梅克尔憩室的供血动脉。栓塞术后,他被转至我院,我们对其进行了急诊剖腹手术,部分切除回肠,包括出血的梅克尔憩室。病理检查发现异位胃黏膜和消化性溃疡,我们认为这是出血的根源。患者术后恢复顺利。内脏动脉瘤虽罕见,但因其有致命破裂的可能性,所以是重要的血管病变。对于无症状梅克尔憩室患者的卵黄肠管动脉瘤,虽然可以进行微创手术,但我们对该患者进行了手术治疗,因为他出现了失血性休克,且对H2受体拮抗剂无反应。