A rare conotruncal anomaly: absent pulmonary valve syndrome, interrupted aortic arch, and severe aortic stenosis.

IF 0.8 4区医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS

Cardiology in the Young Pub Date : 2026-09-30 DOI:10.1017/S1047951126124172

Ghoon Hoong Cheh, Martin Ngie Liong Wong

引用次数: 0

Abstract

The coexistence of absent pulmonary valve syndrome, Type B interrupted aortic arch, and severe aortic stenosis represents an exceptionally rare and complex congenital cardiac phenotype. The diagnosis was established in a newborn using multimodality imaging. Given the profound airway compression secondary to the massive pulmonary artery dilatation and the associated poor prognosis, palliative care was chosen.

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一个罕见的圆锥锥体异常：肺动脉瓣缺失综合征，主动脉弓中断，和严重的主动脉狭窄。

肺动脉瓣缺失综合征、B型主动脉弓中断和严重主动脉瓣狭窄共存是一种非常罕见和复杂的先天性心脏表型。诊断是建立在一个新生儿使用多模态成像。考虑到肺动脉扩张引起的气道深度压迫和预后不良，我们选择了姑息治疗。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Cardiology in the Young 医学-小儿科

CiteScore

1.70

自引率

10.00%

发文量

715

审稿时长

4-8 weeks

期刊介绍： Cardiology in the Young is devoted to cardiovascular issues affecting the young, and the older patient suffering the sequels of congenital heart disease, or other cardiac diseases acquired in childhood. The journal serves the interests of all professionals concerned with these topics. By design, the journal is international and multidisciplinary in its approach, and members of the editorial board take an active role in the its mission, helping to make it the essential journal in paediatric cardiology. All aspects of paediatric cardiology are covered within the journal. The content includes original articles, brief reports, editorials, reviews, and papers devoted to continuing professional development.