[由腹部肿块暴露的髂动脉真菌性动脉瘤]。

Archives francaises de pediatrie Pub Date : 1993-08-01
I Bardi, F Ben Chehida, S Barsaoui, A Hammou, M Ouerghi, S Bousnina, R Slim
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引用次数: 0

摘要

背景:真菌性动脉瘤是感染性心内膜炎的典型并发症。当它们位于深部血管时,诊断可能会很困难。病例报告:一名8岁男孩因腰炎,左髂窝压痛和可触及的肿块而入院。患者因感染性心内膜炎接受抗生素治疗2个月,治疗3周后出现呕吐和发热。血培养为表皮葡萄球菌。肿块的超声检查结果与脓肿相符,但其内容物取样显示有血。即时多普勒超声显示肿块为左髂动脉动脉瘤。该诊断经CT扫描和主动脉造影证实。动脉瘤被切除,并使用Gore-tex移植物进行了满意的修复。结论:虽然该肿块没有临床血管特征,但由于感染性心内膜炎的病史和超声检查结果的更好分析,其起源应得到确认。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Mycotic aneurysm of the iliac artery disclosed by an abdominal mass].

Background: Mycotic aneurysms are classic complications of infective endocarditis. Their diagnosis can be difficult when they are located in deep vessels.

Case report: A 8 year-old boy was admitted for psoitis, tenderness of the left iliac fossa and a palpable mass. He was treated with antibiotics for 2 months for infective endocarditis, but vomiting and fever began after 3 weeks of therapy. Blood cultures showed Staphylococcus epidermidis. Ultrasonography of the mass showed findings compatible with an abscess but sampling of its contents showed blood. Immediate Doppler echography showed that the mass was an aneurysm of the left iliac artery. This diagnosis was confirmed by CT scan and aortography. The aneurysm was excised and a satisfactory repair was made using a Gore-tex graft.

Conclusion: Although this mass had no clinical vascular characteristics, its origin should have been recognized because of the history of infective endocarditis and a better analysis of the ultrasonographic findings.

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