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      An exceptionally large coronary artery aneurysm in a formerly healthy young woman

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          Abstract

          A 32-year-old woman presented with progressive dyspnoea for 6 weeks, fatigue, weight loss, chest pain, and night sweats. Apart from an uncomplicated delivery of her third child 4 months ago, she had no medical or family history. Pneumonia was suspected (chest X-ray Supplementary Fig.1a, b), but thoracic computed tomography (CT) was performed to exclude pulmonary emboli. The CT surprisingly showed a large intrathoracic mass of 94 × 80 mm extending from the sternum to the thoracic spine, compressing the superior and inferior caval veins, the right atrium, and (partly) the right ventricle (Fig. 1, Supplementary Fig. c–e, and Video 1). Further analysis revealed a giant coronary aneurysm (GCA) originating from the proximal right coronary artery (RCA) connecting inferiorly to the distal RCA. Left ventricular function was good (Video 2 and 3). Due to the size and the location of the GCA, surgical exclusion was the treatment of choice (Fig. 2, Supplementary Fig. F). After surgery, the patient recovered well and was discharged on the fifth postoperative day. Fig. 1 Thoracic CT showing a large intrathoracic mass. Note the equal densities of the aneurysm and the left ventricular lumen Fig. 2 Giant coronary aneurysm after sternotomy GCAs are extremely rare: less than 0.02 % of all cardiac surgery is attributed to GCAs [1]. They are usually related to comorbidities or injuries such as infectious disease, inflammatory disease, trauma, coronary angioplasty, or connective tissue disease but can also occur as a congenital abnormality. [4] It is likely that in the current case, the GCA had existed for many years. Increased workload and hormonal changes during pregnancy and delivery may have contributed to growth and symptoms of the GCA [2, 3]. Conflict of interest None declared Electronic supplementary material (JPG 318 kb) (WMV 1271 kb) (AVI 759 kb) (AVI 431 kb)

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          Surgical treatment of giant coronary artery aneurysm.

          Giant coronary artery aneurysm is an extremely uncommon disease. Most previous reports have involved only single cases. This report describes 6 patients with giant coronary artery aneurysm, examines its causes, and aims to establish the optimal surgical strategies for this exceptional and rare pathology. From July 1996 to October 2004, a total of 30,268 patients underwent heart surgery at Fuwai Hospital in Beijing. Among these, 6 patients had giant coronary artery aneurysm diagnosed and underwent operation. Various surgical strategies were used for the operations of these 6 patients, such as coronary artery aneurysm resection, coronary artery reconstruction, and concomitant coronary bypass. Additional procedures, such as fistula closure, aortic valve replacement, aortoplasty, and embolectomy, were done at same time for the patients with complications of coronary fistula, aortic valve insufficiency, or thrombus. Patients were followed up from 8 to 87 months, with a mean of 48 months. Doppler echocardiography, ultrafast computed tomography, and 3-dimensional aerial image studies were performed during follow-up. Five of these six cases were found combined with coronary artery fistula, and the cause for these giant coronary artery aneurysms was congenital. The remaining case was caused by atherosclerosis. After surgery, all patients recovered uneventfully, without in-hospital mortality. None died during the follow-up, nor did any have recurrence of the symptoms or giant coronary artery aneurysm. Giant coronary artery aneurysm is a rare entity that is commonly caused by congenital malformation and combined with other cardiac anomalies. An optimal surgical operation should be based on the specific cardiac anomaly of the individual patient.
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            Histopathologic findings in human aortic media associated with pregnancy.

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              Aorta pathology and pregnancy.

              In addition to the haemodynamic changes in pregnancy, hormones also induce changes in the aortic wall. Women with diseases like Marfan syndrome, Ehlers-Danlo syndrome, or other aortic abnormalities, have an increased risk of complications during pregnancy. Counselling and risk assessment before pregnancy is mandatory for all women with known aortic disease. Proper information should be provided about the risks of morbidity and mortality during pregnancy and information on the risks for the fetus, including the potential recurrence of disease in the offspring. Evaluation of past medical and family history, the aortic size before conception, and any increase in size before and during pregnancy, is essential to try and estimate the risk of aortic dissection. If the aorta is dilated, prophylactic repair before pregnancy may be indicated. In some cases, elective surgery during pregnancy may be warranted. In women with a severely dilated ascending aorta, caesarean section is, at present, the advised mode of delivery.
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                Author and article information

                Contributors
                r.j.hassink@umcutrecht.nl
                Journal
                Neth Heart J
                Neth Heart J
                Netherlands Heart Journal
                Bohn Stafleu van Loghum (Houten )
                1568-5888
                1876-6250
                8 October 2015
                8 October 2015
                December 2015
                : 23
                : 12
                : 609-610
                Affiliations
                [ ]Department of Cardiology, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands
                [ ]Department of Medical Physiology, University Medical Center Utrecht, Utrecht, The Netherlands
                [ ]Department of Radiology, University Medical Center, Utrecht, The Netherlands
                [ ]Department of Anesthesiology, University Medical Center Utrecht, Utrecht, The Netherlands
                [ ]Department of Cardiothoracic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands
                Article
                756
                10.1007/s12471-015-0756-8
                4651965
                26449243
                049f8b1c-40d3-4dd8-a6e8-573f4add6388
                © The Author(s) 2015

                Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

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                Heart Beat
                Custom metadata
                © The Author(s) 2015

                Cardiovascular Medicine
                Cardiovascular Medicine

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