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首页> 外文期刊>Journal of radiology case reports >Transarterial Embolization of a Hepatic Arteriovenous Malformation in an Infant Using Onyx: A Case Report and Review of the Differential Diagnosis Imaging Findings
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Transarterial Embolization of a Hepatic Arteriovenous Malformation in an Infant Using Onyx: A Case Report and Review of the Differential Diagnosis Imaging Findings

机译:On玛瑙婴儿肝动静脉畸形的经动脉栓塞术:一例病例报告及鉴别诊断影像学发现的回顾

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Hepatic arteriovenous malformations are rare congenital lesions associated with significant morbidity and mortality, most commonly from high output cardiac failure. Efficient diagnosis and treatment demands an interdisciplinary approach, and the interventional radiologist plays a pivotal role in both. Imaging is important for diagnostic accuracy and treatment planning, and transcatheter embolization has become an established primary therapy. We report the clinical and imaging findings of a rare hepatic arteriovenous malformation in an infant presenting with high-output cardiac failure and pulmonary artery hypertension that was successfully treated by transarterial embolization using Onyx. Keywords: Arteriovenous malformation, vascular malformation, liver, embolization, Onyx, interventional radiologyCASE REPORTA term male infant was delivered by a 20-year-old woman following an uncomplicated pregnancy. Shortly after delivery, the infant developed tachypnea, pallor, and poor muscular tone. A harsh systolic murmur was detected on physical exam and oxygen saturation was 74%. The patient required emergent intubation.Imaging findingsProfound cardiomegaly and trace bilateral pleural effusions were seen by chest radiography (Fig. 1). Echocardiogram revealed severe right heart dysfunction with atrial septal bowing, marked right atrial enlargement, and paradoxical flow across a patent foramen ovale (Fig. 2). A patent ductus arteriosus with right to left flow and 10 mmHg gradient indicative of pulmonary arterial hypertension was also identified (Fig. 3). Right ventricular function was moderately decreased, but left ventricular function was preserved. A vascular lesion was incidentally found in the liver. Open in a separate windowFigure 1 Conventional radiography.Male newborn with hepatic AVM.FINDINGS: Marked cardiomegaly and trace pleural effusions (arrows).TECHNIQUE: Portable AP chest radiograph. Shimadzu MobileDaRt Evolution.61 kVp. 1 mAs. 40 inches from patient.
机译:肝动静脉畸形是罕见的先天性病变,伴有明显的发病率和死亡率,最常见的原因是高输出心力衰竭。高效的诊断和治疗需要跨学科的方法,而介入放射科医生在这两者中都起着举足轻重的作用。影像学对于诊断准确性和治疗计划很重要,而经导管栓塞术已成为一种已确立的主要疗法。我们报告的临床和影像学发现的罕见的肝动静脉畸形的婴儿表现出高输出心力衰竭和肺动脉高压,已成功通过Onyx经动脉栓塞治疗。关键词:动静脉畸形,血管畸形,肝脏,栓塞,On玛瑙,介入放射学病例报告足月男婴是由一名20岁妇女在无并发症妊娠后分娩的。分娩后不久,婴儿出现呼吸急促,面色苍白和肌肉紧张。体格检查发现严重的收缩期杂音,血氧饱和度为74%。病人需要​​紧急插管。影像学检查发现胸部X线片可见明显的心脏肿大和双侧胸腔积液(图1)。超声心动图显示严重的右心功能不全,伴有心房间隔弯曲,明显的右心房增大以及卵圆孔未闭的反常血流(图2)。还发现了一条动脉导管未闭,从右向左流动,梯度为10 mmHg,表明肺动脉高压(图3)。右心室功能适度降低,但保留了左心室功能。偶然在肝脏中发现了血管病变。在单独的窗口中打开图1常规X线摄片男性患有肝AVM的影像学发现:明显的心脏肥大和微量胸腔积液(箭头)技术:便携式AP胸片Shimadzu MobileDaRtEvolution。61kVp。 1 mAs。离病人40英寸。

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