Down syndrome child with multiple heart diseases: A case report.

IF 1.9 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Mo-Wei Kong, Yi-Jing Li, Jun Li, Zhen-Ying Pei, Yu-Yu Xie, Guo-Xiang He
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引用次数: 0

Abstract

Background: Down syndrome, also known as trisomy 21 syndrome, is commonly associated with congenital heart disease, and can often result in early formation of pulmonary hypertension. The development of pulmonary hypertension can result from factors such as intracardiac and macrovascular shunts, and upper airway obstruction or hypoplasia of lung tissue. Individuals with Down syndrome and congenital heart disease have a significantly lower average life expectancy, with surgical intervention being the most viable treatment option to improve longevity.

Case summary: We report the case of a 13-year-old boy with Down syndrome presenting with atrial septal defect and patent ductus arteriosus along with severe pulmonary hypertension. The electrocardiogram shows sinus rhythm and right ventricular hypertrophy. The echocardiogram shows an atrial septal defect with interrupted echo in the interatrial septum, measuring 0.813 cm in length. The patient was initially refused to be offered surgical treatment by many hospitals due to the high surgical risk and pulmonary artery resistance. After discussing the patient's diagnosis and treatment options, we ultimately recommended surgical treatment. However, the patient and their family declined this recommendation and chose to be discharged. During the follow-up period of 6 mo, there were no significant improvements or deteriorations in the patient's condition.

Conclusion: In conclusion, this case highlights the challenges faced by individuals with Down syndrome and congenital heart disease complicated by severe pulmonary hypertension. Timely intervention and a multidisciplinary approach are crucial for improving prognosis and life expectancy. Further research is needed to enhance our understanding and develop effective interventions for this population.

唐氏综合症儿童合并多重心脏病1例
背景:唐氏综合征,又称21三体综合征,通常与先天性心脏病相关,并可导致肺动脉高压的早期形成。肺动脉高压的发生可由心内和大血管分流、上气道阻塞或肺组织发育不全等因素引起。患有唐氏综合症和先天性心脏病的人平均预期寿命明显较低,手术干预是延长寿命的最可行的治疗选择。病例总结:我们报告一例13岁的唐氏综合症男孩,表现为房间隔缺损和动脉导管未闭,并伴有严重的肺动脉高压。心电图显示窦性心律和右心室肥厚。超声心动图示房间隔缺损,房间隔回声间断,长0.813 cm。由于手术风险高,肺动脉阻力大,患者最初被多家医院拒绝手术治疗。在讨论了患者的诊断和治疗方案后,我们最终建议手术治疗。然而,患者及其家属拒绝了这一建议,选择出院。在6个月的随访期间,患者的病情没有明显的改善或恶化。结论:总之,本病例突出了唐氏综合征和先天性心脏病合并严重肺动脉高压患者所面临的挑战。及时干预和多学科方法对改善预后和预期寿命至关重要。需要进一步的研究来加强我们对这一人群的理解并制定有效的干预措施。
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来源期刊
World Journal of Cardiology
World Journal of Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
3.30
自引率
5.30%
发文量
54
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