Surgical repair of partial atrioventricular septal defect (pAVSD) in adulthood: A rare case report.

IF 0.6 Q4 SURGERY
Agustian Sofian, Rusdiana Rusdiana, Ashil M A Rasyid, Auzan Hakim Agustian
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引用次数: 0

Abstract

Introduction: Partial Atrioventricular septal defect (pAVSD) is a rare congenital heart defect that typically presents in childhood period. It accounts to 1-2 % of all congenital heart malformations with a wide range of presentations from asymptomatic, subtle symptoms to congestive heart failure. While surgical repair is the definitive treatment best achieved at the age of 3-5 years, some patients are diagnosed over this age.

Case presentation: We report a 28-year-old female P1A0 with unremarkable past medical history presented with persistent headache and palpitation for 5 years leading to sleep disturbances. She was initially evaluated by neurologist, but no abnormalities were found. Later she was referred to a pediatric cardiologist and diagnosed as pAVSD because of the existence of primum atrial septal defect (ASD) with mitral valve cleft and mitral regurgitation. The patient was treated with surgical approach. The mitral cleft was repaired with simple interrupted suture, afterwards the primum ASD were closed using pericardial patch. The patient recovered well with subsided symptoms after 6 months of follow-up.

Discussion: The diagnosis of pAVSD may be complex and could constitute a major diagnostic mistake due to the vast range of presentation that may arise. These symptoms are prevalent medical observations noted by clinicians and are mostly benign, commonly alleviated by over-the-counter medications. Delayed diagnosis of pAVSD may postpone final treatment. Untreated pAVSD may progress to pulmonary arterial hypertension, full atrioventricular block, and atrial arrhythmias.

Conclusion: The case presented in this article are one of the many presentations that may appear in adult pAVSD patients. The symptoms were subtle and often harmless medical findings. However, if the symptoms persist, it is recommended to get cardiology consultation and echocardiography, in case suspicion of untreated pAVSD in adulthood arise as one possible differential diagnosis. Albeit she was not at the optimal age for repair, post-operative outcome showed favorable result.

手术修复部分房室间隔缺损(pAVSD):一例罕见的报告。
摘要部分房室间隔缺损是一种罕见的先天性心脏缺损,多见于儿童期。它占所有先天性心脏畸形的1- 2%,表现范围广泛,从无症状,轻微症状到充血性心力衰竭。虽然手术修复是3-5岁时最好的最终治疗方法,但有些患者的诊断年龄超过了3-5岁。病例介绍:我们报告一名28岁的女性P1A0,既往病史一般,表现为持续头痛和心悸5年,导致睡眠障碍。经神经科医生初步检查,未发现异常。后来,她被转到儿科心脏病专家,诊断为房间隔缺损(ASD),二尖瓣裂和二尖瓣反流的存在。患者采用手术入路治疗。单纯间断缝合修复二尖瓣裂,再用心包补片缝合原ASD。随访6个月,患者恢复良好,症状消退。讨论:由于可能出现的广泛表现,pAVSD的诊断可能是复杂的,并且可能构成主要的诊断错误。这些症状是临床医生注意到的普遍医学观察,大多是良性的,通常通过非处方药物缓解。延迟诊断可能会推迟最终的治疗。未经治疗的pAVSD可能发展为肺动脉高压、完全房室传导阻滞和心房心律失常。结论:本文报告的病例是可能出现在成人pAVSD患者中的许多表现之一。这些症状很细微,通常是无害的医学发现。然而,如果症状持续存在,建议进行心脏科咨询和超声心动图检查,如果怀疑成年期未经治疗的pAVSD,作为一种可能的鉴别诊断。虽然她不是最佳的修复年龄,但术后结果良好。
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
CiteScore
1.10
自引率
0.00%
发文量
1116
审稿时长
46 days
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