一名诊断为Wolff-Parkinson-White综合征并伴有心源性休克的新生儿

Jihyun Ha, Sun Hyang Lee, G. Park, Young-Lim Shin, Sung Shin Kim, Mi-Ae Jang
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引用次数: 2

摘要

我们报告了一例健康的28天大的足月女性新生儿,她因严重的代谢性酸中毒、低血糖和最初的窦性心律而住进新生儿重症监护室。第一个诊断假设是低血容量性休克,并立即开始液体复苏。在液体治疗过程中,心血管塌陷伴室上性心动过速。后者用腺苷和β受体阻滞剂成功治疗。8天后,心电图显示心室预激,诊断为Wolff-Parkinson-White综合征。出院后发现了一种与肥厚型心肌病和传导缺陷有关的MYL2基因的新变体。尽管心源性休克是新生儿休克的罕见原因,但仍应考虑。
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A Neonate Diagnosed with Wolff-Parkinson-White Syndrome Presenting with Cardiogenic Shock
We present the case of a healthy 28-day-old female full-term neonate who was admitted to the neonatal intensive care unit for severe metabolic acidosis, hypoglycemia, and an initial sinus rhythm. The first diagnostic hypothesis was hypovolemic shock, and fluid resuscitation was started immediately. During fluid therapy, cardiovascular collapse occurred with supraventricular tachycardia. The latter was successfully treated with adenosine and beta-blockers. After 8 days, electrocardiography showed ventricular pre-excitation, and Wolff-Parkinson-White syndrome was diagnosed. A novel variant of the MYL2 gene that is related to hypertrophic cardiomyopathy and conduction defect was found after discharge. Cardiogenic shock should be considered, despite being a rare cause of shock in neonates.
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审稿时长
12 weeks
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