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1.
J Cardiothorac Surg ; 10: 138, 2015 Oct 30.
Article in English | MEDLINE | ID: mdl-26518127

ABSTRACT

BACKGROUND: Primary cardiac lymphoma is one of the rarest tumours of the heart. It belongs to the extra-nodal non-Hodgkin's lymphomas. The most common type of this tumour is diffuse large B cell lymphoma. Usually, right atrium and right ventricle are involved. This tumour is fatal unless diagnosed and treated in time. In this article two female patients who were diagnosed with primary cardiac lymphoma and treated at our clinic are described. The first patient went to remission after the treatment, while the second patient died. The goals of this article are to show the difficulties of diagnosing and treating this disease, the role of cardiac surgery in its treatment and to raise awareness of this disease. CASE REPORTS: In this article two female patients who were diagnosed with primary cardiac lymphoma and treated at our clinic are described. The first patient went to remission after the treatment, while the second patient died. CONCLUSIONS: Primary cardiac lymphoma is a very rare disease. At the moment the most effective treatment is chemotherapy. Palliative surgery may be necessary to correct hemodynamics when venous blood flow to the lungs is disturbed.


Subject(s)
Heart Neoplasms/diagnosis , Lymphoma, Large B-Cell, Diffuse/diagnosis , Fatal Outcome , Female , Heart Atria/pathology , Heart Neoplasms/surgery , Heart Ventricles/pathology , Humans , Lymphoma, Large B-Cell, Diffuse/surgery , Magnetic Resonance Imaging , Middle Aged , Treatment Outcome
2.
J Cardiothorac Surg ; 10: 72, 2015 May 14.
Article in English | MEDLINE | ID: mdl-25971888

ABSTRACT

Giant congenital right atrial aneurysms are rare defects of the heart. Though usually asymptomatic, they can be potentially life-threatening. Major risks include heart failure, supraventricular arrhythmias, rupture of the wall of the aneurysm. This defect is usually diagnosed incidentally. It is commonly found when transthoracic echocardiography or chest X-ray is performed. In some cases computed tomography or cardiac magnetic resonance imaging is needed to establish the diagnosis. Potential therapeutic options include surgery, catheter ablation and conservative follow-up. Currently preferred method for correcting this defect is surgical excision of the aneurysm, when surgical indications are met. In this article we describe a successful aneurysmectomy performed on a 16-month old female infant, who at the time of hospitalization presented with severe heart failure and symptoms of cardiac tamponade.


Subject(s)
Cardiac Surgical Procedures/methods , Heart Aneurysm/congenital , Heart Aneurysm/surgery , Heart Atria/abnormalities , Heart Atria/surgery , Echocardiography , Echocardiography, Doppler , Female , Heart Aneurysm/diagnosis , Humans , Infant , Magnetic Resonance Imaging, Cine , Tomography, X-Ray Computed
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