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极早产儿肥厚型心肌病。

Hypertrophic cardiomyopathy in an extremely preterm infant.

机构信息

Neonatal Unit, Homerton University Hospital NHS Foundation Trust, London, UK

Neonatal Unit, Homerton University Hospital NHS Foundation Trust, London, UK.

出版信息

BMJ Case Rep. 2021 Mar 9;14(3):e239787. doi: 10.1136/bcr-2020-239787.

Abstract

We present a case of an extreme preterm infant (Baby X) born at 24-week gestation. The echocardiogram showed evidence of hypertrophic cardiomyopathy (HCM) and a patent ductus arteriosus (PDA). There are a number of well-known causes of neonatal HCM including genetic, metabolic and endocrine. PDA is commonly present in preterm infants, and this can contribute to cardiac remodelling and result in cardiac changes mimicking HCM. Furthermore, medications such as steroids can also cause HCM through various mechanisms. A careful consideration of all the different aetiologies for HCM is important for appropriate management of such cases. This report examines the evidence in the literature for the above differential diagnoses and highlights the challenges in diagnosing the underlying cause of HCM in a preterm infant.

摘要

我们呈现了一例 24 周龄极早产儿(婴儿 X)的病例。超声心动图显示肥厚型心肌病(HCM)和动脉导管未闭(PDA)的证据。新生儿 HCM 有许多已知的原因,包括遗传、代谢和内分泌。PDA 在早产儿中很常见,这会导致心脏重塑,并导致类似于 HCM 的心脏变化。此外,类固醇等药物也可以通过各种机制引起 HCM。仔细考虑 HCM 的所有不同病因对于此类病例的适当管理非常重要。本报告检查了文献中关于上述鉴别诊断的证据,并强调了在早产儿中诊断 HCM 潜在病因的挑战。

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Hypertrophic cardiomyopathy in an extremely preterm infant.极早产儿肥厚型心肌病。
BMJ Case Rep. 2021 Mar 9;14(3):e239787. doi: 10.1136/bcr-2020-239787.
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