A case report of spastic diplegic cerebral palsy in a late preterm child with hypoplastic left heart syndrome.

IF 1.5 4区 医学 Q2 PEDIATRICS
Translational pediatrics Pub Date : 2024-07-31 Epub Date: 2024-07-29 DOI:10.21037/tp-24-57
Alexa C Escapita, Julienne G Thomas, Tara L Johnson
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引用次数: 0

Abstract

Background: Congenital heart disease (CHD) is the most common birth defect, affecting 1% of children who are born in the United States each year. Children with hypoplastic left heart syndrome, a type of critical CHD, are at high risk for neurodevelopmental disabilities, which are conditions that can affect motor, language, and cognitive development. In children with critical CHD, the severity and prevalence of their motor delays is most pronounced in infancy.

Case description: We present a case of a former late preterm male with hypoplastic left heart syndrome and history of hypoxic ischemic encephalopathy, who was diagnosed with spastic diplegic cerebral palsy in the setting of periventricular leukomalacia. Like many children with critical CHD, this child had gross motor delays and tone abnormalities in infancy. However, unlike many children with CHD, he continued to have neurologic differences that prompted additional evaluation through a Cardiac Neurodevelopmental Program. He was diagnosed with spastic diplegic cerebral palsy based upon clinical history and physical examination. Ancillary testing showed periventricular leukomalacia on brain magnetic resonance imaging (MRI); this finding was consistent with his clinical diagnosis.

Conclusions: This is an interesting case report of spastic diplegic cerebral palsy in a late preterm infant with critical CHD. When making a diagnosis of cerebral palsy, it is important to consider the etiology of the motor impairment. Selective vulnerability may have played a factor in this child's condition. The most vulnerable part of the neonatal brain is the periventricular white matter; cerebral hypoxia can lead to periventricular leukomalacia. Children with CHD have brain dysmaturity beginning in-utero. Thus, it is possible that this child's brain dysmaturity may have increased his susceptibility to periventricular leukomalacia. Because most children with CHD have gross motor delays in infancy, it may be challenging to make a definitive diagnosis of cerebral palsy in an infant with critical CHD. Children with cerebral palsy have early motor delays that persist throughout life. It is the identification of persistent motor impairments through repeat evaluations that enabled this child's cerebral palsy diagnosis. This illustrates the importance of developmental surveillance in children with critical CHD.

一例早产晚期左心发育不全综合征患儿痉挛性偏瘫脑瘫的病例报告。
背景:先天性心脏病(CHD)是最常见的出生缺陷,每年影响美国1%的新生儿。左心发育不全综合症是一种严重的先天性心脏病,患有该病的儿童是神经发育障碍的高危人群。在患有临界先天性心脏病的儿童中,运动发育迟缓的严重性和普遍性在婴儿期最为明显:我们介绍了一例曾患有左心发育不全综合征和缺氧缺血性脑病的晚期早产男婴,他在脑室周围白斑病的情况下被诊断为痉挛性偏瘫脑瘫。与许多患有危重先天性心脏病的儿童一样,这名儿童在婴儿期也有大运动迟缓和张力异常的症状。然而,与许多患有先天性心脏病的儿童不同的是,他的神经系统仍然存在差异,这促使他接受了心脏神经发育项目的额外评估。根据临床病史和体格检查,他被诊断为痉挛性偏瘫脑瘫。辅助检查显示,脑磁共振成像(MRI)显示存在脑室周围白斑;这一结果与他的临床诊断一致:这是一例有趣的早产儿痉挛性双瘫脑瘫病例报告。在诊断脑瘫时,考虑运动障碍的病因非常重要。选择性脆弱可能是造成该患儿病情的一个因素。新生儿大脑最脆弱的部分是脑室周围白质;大脑缺氧可导致脑室周围白质异常。患有先天性心脏病的儿童从胎儿时期就开始大脑发育不良。因此,该患儿大脑发育不全可能会增加他对脑室周围白质异常症的易感性。由于大多数患有先天性心脏病的儿童在婴儿期都会出现粗大运动迟缓,因此对患有严重先天性心脏病的婴儿做出脑瘫的明确诊断可能具有挑战性。脑瘫患儿的早期运动迟缓会持续终生。正是由于通过重复评估发现了持续性运动障碍,该患儿才得以确诊为脑瘫。这说明了对患有严重先天性心脏病的儿童进行发育监测的重要性。
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
Translational pediatrics
Translational pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
4.50
自引率
5.00%
发文量
108
期刊介绍: Information not localized
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