先天性单侧心包发育不全表现为青少年孤立性胸痛:一例报告和综合回顾。

IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Farshad Jafari, Maryam Taheri, Pouya Ebrahimi, Maedeh Soflaee, Reyhaneh Alipore Rafie, Mohsen Anafje
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引用次数: 0

摘要

摘要先天性心包发育不全是一种罕见的先天性异常,是由于胚胎发生时胸膜心包膜发育不全,导致心包囊部分或完全缺失所致。虽然这种情况通常没有症状,但它可以表现出各种误导性的症状,如胸痛(加上其他一些,可能是2个,更普遍的症状),使诊断具有挑战性。先进的成像技术对于准确的诊断和管理至关重要,特别是当常规诊断方式不能达到明确的诊断时。病例介绍:我们详细介绍了一位16岁女性的病史和诊断过程,她表现为孤立的非运动性胸痛。开始进行全面的诊断检查,包括胸部x线(CXR)、经胸超声心动图(TTE)、CT血管造影(CTA)和心脏磁共振成像(CMRI)。这些先进的成像模式揭示了罕见且难以捉摸的左侧心包发育不全的诊断,果断地排除了其他潜在的原因,并揭示了一个挑战传统诊断途径的特殊病例。结论:单侧心包发育不全,虽然通常是良性的,且常被临床所掩盖,但可表现出难以理解的症状,如孤立性胸痛,需要细致而全面的诊断方法。多模态成像对于准确诊断和排除心脏疝或冠状动脉压迫等并发症至关重要。考虑到没有明显的并发症,本病例选择保守治疗,患者出院时指示监测任何警告信号。临床关键信息:临床医生应考虑先天性心包发育不全是不明原因胸痛的潜在原因之一,特别是当初步调查尚无结论时。先进的成像技术(如CXR和MRI)对于确认诊断以及随后适当和及时的管理和预防潜在的并发症至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital unilateral pericardial agenesis presenting as an isolated chest pain in an adolescent: a case report and comprehensive review.

Introduction: Congenital pericardial agenesis is a rare congenital anomaly resulting from the incomplete development of the pleuropericardial membranes during embryogenesis, leading to the partial or complete absence of the pericardial sac. Although this condition usually remains asymptomatic, it can present with various misleading symptoms such as chest pain (add some other, maybe 2, more prevalent presenting symptoms), making diagnosis challenging. Advanced imaging techniques are crucial for accurate diagnosis and management, especially when usual diagnostic modalities do not achieve a definite diagnosis.

Case presentation: The history and diagnostic process of a 16-year-old female who presented with isolated, non-exertional chest pain are detailed. A comprehensive diagnostic work-up was initiated, including chest X-ray (CXR), transthoracic echocardiogram (TTE), CT angiography (CTA), and cardiac magnetic resonance imaging (CMRI). These advanced imaging modalities unveiled the rare and elusive diagnosis of left-sided pericardial agenesis, decisively ruling out other potential causes and shedding light on an extraordinary case that challenges conventional diagnostic pathways.

Conclusion: Unilateral pericardial agenesis, though typically benign and often shrouded in clinical obscurity, can manifest with enigmatic symptoms such as isolated chest pain, necessitating a meticulous and comprehensive diagnostic approach. Multimodal imaging is essential for accurate diagnosis and for ruling out complications such as cardiac herniation or coronary artery compression. Considering the absence of significant complications, conservative management was chosen in this case, with the patient being discharged with instructions to monitor for any warning signs.

Clinical key message: Clinicians should consider congenital pericardial agenesis as one of the potential causes of unexplained chest pain, particularly when the initial investigations are inconclusive. Advanced imaging techniques (such as CXR and MRI) are vital for confirming the diagnosis and subsequently appropriate and timely management and preventing potential complications.

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来源期刊
Journal of Cardiothoracic Surgery
Journal of Cardiothoracic Surgery 医学-心血管系统
CiteScore
2.50
自引率
6.20%
发文量
286
审稿时长
4-8 weeks
期刊介绍: Journal of Cardiothoracic Surgery is an open access journal that encompasses all aspects of research in the field of Cardiology, and Cardiothoracic and Vascular Surgery. The journal publishes original scientific research documenting clinical and experimental advances in cardiac, vascular and thoracic surgery, and related fields. Topics of interest include surgical techniques, survival rates, surgical complications and their outcomes; along with basic sciences, pediatric conditions, transplantations and clinical trials. Journal of Cardiothoracic Surgery is of interest to cardiothoracic and vascular surgeons, cardiothoracic anaesthesiologists, cardiologists, chest physicians, and allied health professionals.
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