Abstract:Superior vena cava syndrome is a life-threatening condition. Typically, the clinical presentations are gradual; hence, the diagnosis is often delayed until critical compression or obstruction has occurred. Pericardial hematoma is a rare condition that could occur after cardiac surgery. An asymptomatic, 25-year-old female, who underwent surgical atrial septal defect closure 5 days ago, was sent for routine echocardiography examination before discharge. An intrapericardiac hematoma was detected at the right atri… Show more
“…Mediastinal hematoma caused due to damage from epicardial wires of CABG is an uncommon but significant complication [4,5]. Mediastinal hematoma with sufficient volume may result in compression of the neighboring heart chambers or vessels, one of which could be superior vena cava leading to the superior vena cava syndrome [5].…”
Section: Discussionmentioning
confidence: 99%
“…The computed tomography angiography (CTA) chest revealed a hematoma with an active extravasation within the right superior anterior mediastinum measuring 6 x 8 x 4 cm, outside the pericardium, and helped rule out hemopericardium. The imaging, just like in Figure 1, also showed that the posteriorly superior vena cava was compressed [4,5]. Due to the presence of hemorrhage adjuvant to epicardial pacer leads, it was proposed as a possible etiology for hemorrhage.…”
Section: Case Presentationmentioning
confidence: 93%
“…Source: Saboe et al [4] SVC: superior vena cava CT brain showed no abnormality. An echocardiogram showed an ejection fraction of 60% and confirmed the absence of hemopericardium.…”
“…These symptoms can be gradually progressing and are very often missed [2]. The superior vena cava syndrome is also known to cause sudden death [3,4].…”
“…Mediastinal hematoma caused due to damage from epicardial wires of CABG is an uncommon but significant complication [4,5]. Mediastinal hematoma with sufficient volume may result in compression of the neighboring heart chambers or vessels, one of which could be superior vena cava leading to the superior vena cava syndrome [5].…”
Section: Discussionmentioning
confidence: 99%
“…The computed tomography angiography (CTA) chest revealed a hematoma with an active extravasation within the right superior anterior mediastinum measuring 6 x 8 x 4 cm, outside the pericardium, and helped rule out hemopericardium. The imaging, just like in Figure 1, also showed that the posteriorly superior vena cava was compressed [4,5]. Due to the presence of hemorrhage adjuvant to epicardial pacer leads, it was proposed as a possible etiology for hemorrhage.…”
Section: Case Presentationmentioning
confidence: 93%
“…Source: Saboe et al [4] SVC: superior vena cava CT brain showed no abnormality. An echocardiogram showed an ejection fraction of 60% and confirmed the absence of hemopericardium.…”
“…These symptoms can be gradually progressing and are very often missed [2]. The superior vena cava syndrome is also known to cause sudden death [3,4].…”
“…The differential diagnosis of a pericardial mass is challenging, and both benign and malignant (primary or metastatic) diseases should be considered [31]. Heterogenous non-neoplastic pericardial entities (hematomas, thrombi, pseudoaneurysms, cysts, and inflammatory pseudo tumours) are described in the literature [32], as is the contribution of multimodality imaging in the diagnosis of multiple pericardial hematomas and the development of progressive superior vena cava syndrome [33,34]. However, the literature to date has not described the presence of a pericardial haematoma secondary to chronic TAAD compressing the right atrium and the superior and inferior caval veins, leading to right heart failure.…”
Background
An intrapericardial organized haematoma secondary to chronic type A aortic dissection is an extremely rare cause of right heart failure. Imaging studies are essential in recognising and diagnosis of this distinctive medical condition and guiding the anticipated treatment.
Case presentation
A 70-year-old male patient was admitted for progressive symptoms of right heart failure. His cardiovascular history exposed an aortic valve replacement 22 years before with a Medtronic Hall 23 tilting valve with no regular follow-up. Classical signs of congestion were recognized at physical examination. Transthoracic two-dimensional echocardiography and thoraco-abdominal computed tomography angiography, as essential parts of multimodality imaging algorithm, established the underlying cause of right heart failure. Under total cardiopulmonary bypass and cardiac arrest, surgical removal of the haematoma and proximal repair of the ascending aorta with a patient-matched vascular graft were successfully performed. The patient was discharged in good condition with appropriate pharmacological treatment, guideline-directed; no imagistic signs of acute post-surgery complications were ascertained.
Conclusion
This paper highlights the importance of recognizing and providing a timely clinical and imagistic diagnosis of this very rare, potentially avoidable cause of right heart failure in patients with previous cardiac surgery.
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