Navigating complexity: ruptured pulmonary artery dissection originating from type B aortic dissection via a persistent ductus arteriosus Botalli.

Matthias N Hagedorn, Andreas S Peters, Katrin Meisenbacher, Philipp Erhart, Moritz S Bischoff, Peter Reimer, Matthias Karck, Matthias Gorenflo, Dittmar Böckler
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引用次数: 0

Abstract

Pulmonary artery dissection (PAD) is a rare, life-threatening condition requiring prompt diagnosis and treatment. We present a case of ruptured left PAD originating from an acute type B aortic dissection (aTBAD) through a persistent ductus arteriosus Botalli (PDA) in an otherwise healthy 29-year-old man. The patient was successfully treated by means of thoracic endovascular aortic repair (TEVAR) alone. This case illustrates a rare and severe cardiovascular emergency, highlighting the critical importance of interdisciplinary collaboration. For the first time, we demonstrated that addressing the root of the problem - the primary aortic entry - leads to full symptom resolution and vascular remodeling.

导航复杂性:B型主动脉夹层经持续性波塔利动脉导管引起的肺动脉夹层破裂。
肺动脉夹层(PAD)是一种罕见的危及生命的疾病,需要及时诊断和治疗。我们报告一例由急性B型主动脉夹层(aTBAD)引起的左外周动脉破裂,该动脉夹层通过持续性的波塔利动脉导管(PDA),患者为29岁健康男性。仅采用胸椎血管内主动脉修复术(TEVAR)即可成功治疗。该病例说明了一种罕见而严重的心血管急症,突出了跨学科合作的至关重要性。第一次,我们证明了解决问题的根源-主主动脉入口-导致症状的完全解决和血管重塑。
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