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首页> 外文期刊>Journal of the American College of Radiology: JACR >ACR Appropriateness Criteria Clinically Suspected Pulmonary Arteriovenous Malformation
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ACR Appropriateness Criteria Clinically Suspected Pulmonary Arteriovenous Malformation

机译:临床可疑的ACR适当标准肺动静脉畸形

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摘要

Pulmonary arteriovenous malformations are often included in the differential diagnosis of common clinical presentations, including hypoxemia, hemoptysis, brain abscesses, and paradoxical stroke, as well as affecting 30% to 50% of patients with hereditary hemorrhagic telangiectasia (HHT). Various imaging studies are used in the diagnostic and screening settings, which have been reviewed by the ACR Appropriateness Criteria Vascular Imaging Panel. Pulmonary arteriovenous malformation screening in patients with HHT is commonly performed with transthoracic echocardiographic bubble study, followed by CT for positive cases. Although transthoracic echocardiographic bubble studies and radionuclide perfusion detect right-to-left shunts, they do not provide all of the information needed for treatment planning and may remain positive after embolization. Pulmonary angiography is appropriate for preintervention planning but not as an initial test. MR angiography has a potential role in younger patients with HHT who may require lifelong surveillance, despite lower spatial resolution compared with CT.
机译:肺动静脉畸形通常包括在常见临床表现的鉴别诊断中,包括低氧血症,咯血,脑脓肿和自相矛盾的中风,并影响30%至50%的遗传性出血性毛细血管扩张症(HHT)患者。诊断和筛查设置中使用了各种成像研究,这些研究已由ACR适当性标准血管成像小组进行了审查。 HHT患者的肺动静脉畸形筛查通常是通过经胸超声心动图气泡研究进行的,对于阳性病例,应行CT检查。尽管经胸超声心动图泡沫研究和放射性核素灌注检测从右向左分流,但它们不能提供治疗计划所需的所有信息,栓塞后可能仍呈阳性。肺血管造影适合进行干预前的计划,但不适合作为初始检查。尽管与CT相比空间分辨率较低,但MR血管造影术在可能需要终生监护的年轻HHT患者中具有潜在作用。

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