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小儿外科影像。罕见病例:无症状儿童的腹腔干压迫综合征。

Pediatric surgical image. A rare case: celiac artery compression syndrome in an asymptomatic child.

作者信息

Alehan Dursun, Dogan Omer Faruk

机构信息

Hacettepe University Medical Faculty, Ankara, Turkey.

出版信息

J Pediatr Surg. 2004 Apr;39(4):645-7. doi: 10.1016/j.jpedsurg.2003.12.037.

Abstract

Celiac artery compression syndrome is a rare disorder and characterized by postprandial intestinal angina caused by insufficient blood supply to the gastrointestinal organs in symptomatic patients. This pathology is also known as median arcuate syndrome. The authors report a case of 12-year-old boy with severe celiac artery compression by the median arcuate ligament that was diagnosed by Magnetic Resonance Angiography (MRA) and color dupplex ultrasonography (US). There was only a bruit in the upper midepigastrium, and there were no gastrointestinal symptoms despite severe compression of celiac trunk. This clinicopathologic entity is very rare but represents severe complaints and clinical results caused by a decreased rate of the intestinal blood flow. In this report the authors suggest that the diagnosis of celiac artery compression should be considered in asymptomatic pediatric patients representing abdominal bruit or with palpated thrill in the upper epigastrium. In comparison with case reports present in the English-language literature, the patient reported on here is the youngest diagnosed.

摘要

腹腔动脉压迫综合征是一种罕见的疾病,其特征是有症状的患者因胃肠道器官血液供应不足而出现餐后肠绞痛。这种病理状况也被称为正中弓状韧带综合征。作者报告了一例12岁男孩,其腹腔动脉被正中弓状韧带严重压迫,通过磁共振血管造影(MRA)和彩色双功超声检查(US)得以确诊。仅在上腹部中部有杂音,尽管腹腔干严重受压,但并无胃肠道症状。这种临床病理实体非常罕见,但代表了因肠血流量减少而引起的严重症状和临床后果。在本报告中,作者建议对于有腹部杂音或上腹部可触及震颤的无症状儿科患者,应考虑腹腔动脉压迫的诊断。与英文文献中现有的病例报告相比,此处报告的患者是确诊时年龄最小的。

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