Description

A 42-year-old female with a history of migraine was admitted to our hospital with syncope at rest. She had a 1-week history of dizziness, fatigue, headache and right lower limb pain. At physical examination she had a body mass index of 33.6 kg/m², oedema of the right lower limb, and her blood pressure was 100/69 mm Hg, with 95% oxygen saturation. Troponin I was 0.1 ng/ml (normal<0.034 ng/ml) and NT-proBNP was 5260 pg/ml (normal<1800 pg/ml). An ECG showed sinus tachycardia with 110 bpm and negative T-waves in inferior and anterior leads. A Doppler ultrasound of the right lower limb confirmed the diagnosis of deep venous thrombosis. A transthoracic echocardiography documented a very mobile, irregular, heterogeneous and huge (1 cm×1.8 cm) mass in the right atria crossing the interatrial septum and intermittently the mitral valve, swinging between the left atria and left ventricle (videos 1–3). There was also a heterogeneous mass in the right branch of the pulmonary artery, enlargement and hypokinesia of the right ventricle, interventricular septal rectification, moderate tricuspid regurgitation and an estimated pulmonary artery systolic pressure of 83 mm Hg (figures 1 and 2). A chest CT scan confirmed bilateral pulmonary thromboembolism (figure 3). Perfusion of alteplase was started but was discontinued after half the dosage (50 mg) owing to a massive haematoma of the neck with dysphagia. After consulting a thoracic surgeon, a continuous infusion of unfractionated heparin was started, with a complete resolution of the mass in 3 days (confirmed on transesophageal echocardiogram). As the patient complained of a severe and persistent migraine-like headache, a cranial magnetic resonance was performed 14 days after the admission to rule out paradoxical embolism or treatment-related intracranial bleeding (figure 4). The examination showed small high-signal foci in the supratentorial white matter compatible with multiple small strokes. The serological screening carried out for thrombophilia, autoimmune diseases and vasculitis was negative. The patient was discharged without any neurological deficits after percutaneous closure of the patent foramen ovale under hypocoagulation.

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Figure 1

Transthoracic echocardiography performed in the emergency room, in a four-chamber view, showing the thrombus on both sides of the interatrial septum (A) and crossing the mitral valve during diastole (B). RV, right ventricle; LV, left ventricle; RA, right atria; LA, left atria; the arrows indicate the thrombus.

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Figure 2

Transthoracic echocardiography performed in the emergency room. (A) In a longitudinal short-axis view demonstrating the thrombus on both sides of the interatrial septum; (B) In a longitudinal long-axis view showing the thrombus crossing the mitral valve in diastole (B). RV, right ventricle; LV, left ventricle; RA, right atria; LA, left atria; Ao, aorta; the arrows indicate the thrombus.

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Figure 3

Chest angio-CT scan obtained 3 h after the admission. (A) In an axial plane, identifying a filling defect in both branches of the pulmonary artery, confirming a diagnosis of pulmonary embolism; (B) In a volume-rendered endocardial view, showing the thrombus through the suspected defect in the interatrial septum. Ao, aorta; PA, pulmonary artery; RB, right branch; LB, left branch; RV, right ventricle, LV, left ventricle; RA, right atria; LA, left atria; the arrows indicate the thrombus.

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Figure 4

Transesophageal echocardiography performed 15 days after the admission, obtained at 55°, confirming the presence of a patent foramen ovale. (A) During the microbubbles test; (B) With colour doppler. Ao, aorta; LA, left atria; RA, right atria; the arrow indicates the patent foramen ovale.