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经努森伦塞钠治疗的 2 型脊髓性肌萎缩症患儿行室间隔缺损的外科矫正:病例报告。

Surgical correction of a ventricular septal defect in a child with spinal muscular atrophy type 2 treated with nusinersen sodium: a case report.

机构信息

Department of Pediatric Cardiovascular Surgery, Koç University Hospital, Istanbul, Turkey.

School of Medicine, Koç University, Koç University Hospital, Zeytinburnu, Istanbul, Turkey.

出版信息

J Cardiothorac Surg. 2023 Feb 9;18(1):68. doi: 10.1186/s13019-023-02170-z.

Abstract

INTRODUCTION

Spinal muscular atrophy (SMA) is a severe, inherited neuromuscular disorder characterized by progressive muscle weakness and atrophy. Cardiac pathology co-existence is reported more frequently in the severely affected patient groups. Structural heart anomalies, mainly septal, and outflow tract defects are commonly observed pathologies.

CASE PRESENTATION

We herein report the case of a 23 days-old female patient with the diagnosis of spinal muscular atrophy type 2 complicated with structural heart defects. Successful pulmonary banding, and at the age of 17 months, subsequent surgical atrial and ventricular septal defect closure were performed on our patient who was under treatment of Nusinersen Sodium. Post-operative recovery was uncomplicated. Cardiac assessments were normal, and the patient was neurologically improving in her recent follow-up.

CONCLUSION

In the literature, there are no reported cases of successful surgical repair of heart defects in spinal muscular atrophy patients. These patients can be perceived as risky surgical candidates with suboptimal postoperative recovery given the unfavorable disease prognosis of SMA in untreated patients. We report our promising experience with a SMA type 2 patient undergoing a disease-modifying medical treatment. The SMA patients under treatment may be potential candidates for successful surgical cardiac correction given their overall improved prognosis.

摘要

介绍

脊髓性肌萎缩症(SMA)是一种严重的遗传性神经肌肉疾病,其特征是进行性肌肉无力和萎缩。在病情严重的患者群体中,心脏病理学共存的报告更为频繁。结构心脏异常,主要是间隔和流出道缺陷,是常见的病理学观察结果。

病例介绍

我们在此报告一例 23 天大的女性患者,诊断为 2 型脊髓性肌萎缩症,合并结构心脏缺陷。我们对患者成功地进行了肺动脉环缩术,在 17 个月大时,在使用 Nusinersen Sodium 治疗的同时,对其进行了心房和心室间隔缺损的后续手术修复。术后恢复顺利。心脏评估正常,在最近的随访中,患者的神经功能在改善。

结论

在文献中,没有报道过成功修复脊髓性肌萎缩症患者心脏缺陷的病例。鉴于未治疗患者 SMA 疾病预后不佳,这些患者可能被视为风险较高的手术候选者,术后恢复情况不佳。我们报告了一例 2 型 SMA 患者的有希望的经验,该患者接受了疾病修正治疗。接受治疗的 SMA 患者由于整体预后改善,可能是成功进行心脏矫正手术的潜在候选者。

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本文引用的文献

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Spinal muscular atrophy: mechanisms and therapeutic strategies.脊髓性肌萎缩症:发病机制与治疗策略。
Hum Mol Genet. 2010 Apr 15;19(R1):R111-8. doi: 10.1093/hmg/ddq147. Epub 2010 Apr 13.

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