Huge Thoracic Aortic Aneurysm Presenting with Jaundice: A Case Report.

INTRODUCTION: Thoracic aortic aneurysms (TAA) are encountered frequently in the emergency department with an obscure presentation. Most of these aneurysms are incidentally discovered while doing routine imaging studies. This report describes a case of unusual presentation of TAAs. CASE
PRESENTATION: A 37-year-old male presented to the emergency department with jaundice, shortness of breath, abdominal swelling, and lower limb edema, which worsened during the previous month. The patient was worked up and diagnosed with an ascending aortic aneurysm measuring 6.9 cm associated with severe aortic insufficiency and heart failure.
CONCLUSION: TAA is a life-threatening condition with indistinct signs and symptoms. A high index of suspicion and early implementation of radiological studies are prerequisites to reach a diagnosis.

Background

Thoracic aortic aneurysms are often silent.1–4 Their diagnosis usually follows a pathway in which a radiological study is being performed for a different reason, and the aneurysm is discovered coincidentally.5 The etiology of aneurysmal formation is incompletely understood.6 Most aortic aneurysms are caused by degenerative, infectious, or genetic conditions that weaken the aortic wall.6 Symptomatic aortic aneurysms may manifest as chest pain, discomfort, a new cardiac murmur, or more drastically as heart failure, aortic dissection, or rupture.6 It is estimated that 21% of patients suffering from acute aortic syndromes die before reaching the hospital.2 Jaundice is mainly caused by choledocholithiasis, carcinoma of the head of the pancreas, biliary strictures, pancreatitis, and sclerosing cholangitis.7 Jaundice is a rare presentation of abdominal aneurysms due to obstruction to the biliary tree.7 CT or MRI confirms the diagnosis of aortic aneurysms.6 Intervention by surgery or percutaneous technology is indicated when the size of the aneurysm reaches a threshold where the risk for developing complications according to the natural history of the disease is significant.6,8

Case Presentation

A 37-year-old man who smokes but denies any previous medical illness was referred to Prince Sultan Cardiac Center complaining of worsening shortness of breath, especially during exertion, abdominal swelling, and lower limb edema. He has no family history of connective tissue disorders. Upon examination, the patient looked tired, jaundiced, and unable to lie flat on the bed. The patient was afebrile. His heart rate was 113 beats per minute, his blood pressure was 101/70 mmHg, and he saturated 97% on room air. On chest auscultation, there was an audible diastolic murmur all over the chest. The abdominal exam was unremarkable, and there was bilateral pitting edema up to the shaft of the leg. Laboratory investigations showed the following: hemoglobin of 13 g/dl, normal platelet count, elevated liver enzymes with AST of 843 U/L (Normal: 0–32 U/L), ALT 1766 U/L (Normal 0–41 U/L), total bilirubin of 290 umol/L (Normal: 0–21 umol/L), and direct bilirubin of 200 umol/L (Normal: 0–3.4 umol/L). Creatinine was also elevated at 120 umol/L (Normal: 62–106 umol/L). The coagulation profile was abnormal, with INR 2.15 sec., while cardiac enzymes were within normal. The patient’s chest x-ray showed an enlarged cardiac silhouette (Figure 1). The abdominal ultrasound was normal. The patient had transthoracic echocardiography (TTE), which showed severely reduced ventricular function with an ejection fraction of about 25%, dilated both ventricles, a bicuspid aortic valve with severe regurgitation, dilated inferior vena cava, congested liver, and an ascending aortic aneurysm with a maximum diameter of 6.9 cm (Figure 2). CT scan with contrast further delineated the aneurysm and its extension into the distal aorta, which was only confined to the ascending aorta (Figure 3). Following an urgent heart team discussion, the patient was admitted to the intensive care unit for close observation and started on intravenous inotropes to support his circulation and optimize his condition for surgery. His blood pressure was maintained at less than 120 mmHg, and his heart rate was sustained to 55 beats per minute. The patient underwent a modified Bentall procedure in the second week of admission. The surgery was uneventful, and the patient was discharged home one week post-surgery. Tissue pathology showed degenerative changes only. The follow-up echo four weeks later demonstrated improvement in overall cardiac function, and the patient reported significant symptomatic improvement.

Figure 1

Chest X-ray showing enlarged cardiac silhouette with cardiothoracic ratio of 70%, and mild pulmonary congestion.

Figure 2

Transthoracic echocardiography; (A) parasternal long axis view showing an ascending aortic aneurysm (#) and (B) subcostal view showing dilated inferior vena cava (**) and congested liver (***).

Figure 3

CT chest axial view showing a huge ascending aortic aneurysm (*).

Discussion

An aneurysm can generally be defined as the enlargement of a blood vessel to more than 150% of the diameter expected for gender, age, and weight.4 Although the true prevalence of TAAs is unknown, it is estimated to have an incidence of at least 5–10 per 100,000 person-years.5,9 More than half of these aneurysms are in the ascending aorta followed in frequency by the descending thoracic aorta. Less than 10% are confined to the aortic arch.5 Atherosclerosis along with its risk factors, connective tissue disease (eg, Marfan syndrome), and abnormalities of the aortic valve (eg, bicuspid aortic valve) are strongly associated with the development of ascending aortic aneurysms, but sporadic cases have also been reported.10,11

The majority of TAAs are asymptomatic, and identifying a patient with them represents a true challenge to health care providers.4,5 TAA can be encountered during a routine radiological examination, as an acute presentation with dissection, as a part of screening the relative of a patient with a known aneurysm, or as a part of a known congenital cardiac defect.1 Frequently reported symptoms of thoracic aortic aneurysm include dyspnea, cough, dysphagia, hoarseness of voice, claudication, cerebrovascular events, as well as chest, abdominal, or back pain.11 Other unusual presentations of thoracic aneurysms reported in the literature include erosion of the overlying skin and sternum, rupture into the esophagus, compression and invasion of the pulmonary artery, superior vena cava syndrome, and recurrent laryngeal and phrenic nerve palsy.12–15,17,18 The most common causes of jaundice are choledocholithiasis, biliary strictures, carcinoma of the head of the pancreas, pancreatitis, and sclerosing cholangitis.7 Jaundice has been reported in the literature as a rare presentation of abdominal aortic aneurysm (not TAAs) because of compression and obstruction of biliary ducts.16 Right ventricular failure may precipitate liver congestion, while congestion reduces hepatic blood flow, decreases arterial oxygen saturation, and increases hepatic venous pressure.19 Laboratory abnormalities include elevated serum aminotransferase level to two to three times the upper limit of normal and hyperbilirubinemia.19 In our case, the patient developed biventricular failure, which resulted in hepatic congestion, and consequently, jaundice.

Unrecognized aneurysms risk rupture and dissection, which carry higher morbidity and mortality burden.18 To diagnose these aneurysms, the clinical history should be focused on the symptoms, risk factors, family history, and followed by detailed physical examination looking for signs of aneurysmal dilatation or its complications.11 Aortic imaging with echocardiography, computed tomography angiography, and magnetic resonance angiography remain the cornerstone to diagnose aortic aneurysms.11 Screening with transesophageal echocardiography is reasonable to evaluate the aorta in predisposed populations (eg, connective tissue disorders, bicuspid aortic valve, or screening first-degree relatives of patients with TAA). There is no recommendation for screening the general population.5 Blood pressure control is the cornerstone of nonsurgical management of small uncomplicated aneurysms.18 The significant determinants for intervention are the size of the aneurysm, rate of expansion, and associated conditions.11 Aneurysms are repaired when the risk of rupture exceeds the risk of repair.5

Conclusion

The presentation of TAAs can be obscured. Focused clinical history, physical examination, and early implementation of diagnostic imaging aid in early recognition and management of aneurysms and avoid significant morbidity and mortality.