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      Unsolved Enigma of Atrial Myxoma with Biventricular Dysfunction

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          Abstract

          The Editor, Cardiac myxoma is the most common primary cardiac tumor. However, it is very unusual to find cardiac myxoma with severe biventricular dysfunction. We congratulate the authors for successful management of such cases.[1] Coexisting coronary atherosclerosis and coronary embolization of tumor fragments causing myocardial ischemia are well-known reasons for ventricular dysfunction in patients with left atrial myxoma. The incidence of coronary artery disease in patients with myxoma is between 20.3% and 36.6%.[2 3] Other proposed explanations for the left ventricular dysfunction in such patients were hypercoagulability state in patients with myxoma and raised interleukin-6.[3] Cases reported by Tewari et al. did not undergo preoperative coronary angiography. The reason, we believe, may be younger age groups and hence coronary artery disease was not suspected. Interestingly ventricular function improved immediately after the removal of myxoma. Previously we reported a case of left atrial myxoma with biventricular dysfunction despite having normal coronaries angiographically.[4] However, ventricular function didn’t improve even after removal of tumor. We believe that undiagnosed concomitant dilated cardiomyopathy could have been the reason. Cardiac myxoma is classified into two types. Type 1 myxoma is with an irregular villous or papillary surface and a soft consistency, and type 2 myxoma is with a smooth surface and a compact consistency.[3] Type 1 myxoma is more common and more fragile and tend to embolize frequently than myxomas with a smooth surface.[3] It is also suggested that repeated impingements of myxoma against the atrial wall or the valve leaflets can form thrombus leading to embolic events.[3] Embolic potential from a cardiac myxoma is mainly influenced by mobility and friability rather than tumor size.[3] Another plausible hypothesis for ventricular dysfunction in cardiac myxoma is coronary steal phenomenon due to highly vascularized mass in the cardiac chamber.[2] In a study of myxoma-related acute myocardial infarction (AMI), it was found that 48.8% of these patients had normal coronary arteries in coronary angiogram.[3] Although causes of the normal coronary angiogram in patients with cardiac myxoma-related AMI remain elusive, author suggested higher spontaneous recanalization rates of the myxomatous embolization as feasible explanation owing to rapid breakdown of the myxomatous materials.[3] Anecdotal case reports have suggested the reversal of cardiac dysfunction after surgical removal of myxoma suggesting the possibility of myocardial depressant effect of myxoma unrelated to coronary occlusion.[5] In young patients without apparent risk factors of coronary artery disease presenting with AMI and/or ventricular dysfunction, cardiac myxoma should always be placed as one of the differential diagnosis. Although echocardiography evaluates the myxoma in cardiac chambers, coronary angiography is important in identifying the status of coronary emboli and helps in decision-making for further management. surgically removed myxoma should be subjected to histopathological examination for diagnosis but also the structure should also evaluated for histochemical analysis for cardio-depressant factors particularly in patients with ventricular dysfunction. Endomyocardial biopsy in such patients during the surgery can also help to rule out associated cardiomyopathy. Future studies are certainly warranted in patients with cardiac myxoma with ventricular dysfunction. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.

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          Cardiac myxoma: a rare cause of acute myocardial infarction

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            Severe left ventricular dysfunction in left atrial myxoma--report of 2 cases.

            We report 2 patients with left atrial (LA) myxoma with associated severe left ventricular (LV) dysfunction. Both presented with progressive effort intolerance without a history suggestive of acute coronary event. LA myxoma was diagnosed by transthoracic echocardiography, which also detected severe systolic dysfunction and LV dilatation. Regional wall motion abnormality and thinning were absent. Coronary angiograms also showed no occlusive disease, but distal ectasia was seen in 1 patient. Metabolic and endocrine causes of reversible LV dysfunction were excluded. Cardiac function improved following surgery for myxoma in 1 patient. LV dysfunction, thus far, has not been directly attributed to myxoma. Coronary embolization leading to myocardial infarction and coexisting coronary atherosclerosis are the recognized methods by which LV dysfunction manifests in myxoma. Our report suggests the possibility of reversible severe global LV dysfunction due to cardiodepressant effect of myxoma through as yet unclear mechanisms.
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              Atrial Myxomas Causing Severe Left and Right Ventricular Dysfunction

              Myxomas are the most common cardiac tumors, accounting for about 50% of benign primary cardiac tumors, with the majority located in the left atrium, and 80% of which originate in the interatrial septum. We report two cases with severe cachexia, neurological sequelae, and severe biventricle dysfunction secondary to atrial myxomas with marked early improvement after tumor excision.
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                Author and article information

                Journal
                Ann Card Anaesth
                Ann Card Anaesth
                ACA
                Annals of Cardiac Anaesthesia
                Medknow Publications & Media Pvt Ltd (India )
                0971-9784
                0974-5181
                Jan-Mar 2018
                : 21
                : 1
                : 105-106
                Affiliations
                [1] Department of Cardiac Anaesthesia, Sir Ganga Ram Hospital, New Delhi, India
                [1 ] Department of Cardiac Surgery, Sir Ganga Ram Hospital, New Delhi, India
                Author notes
                Address for correspondence: Dr. Monish S Raut, Department of Cardiac Anaesthesia, Sir Ganga Ram Hospital, New Delhi, India. E-mail: drmonishraut@ 123456gmail.com
                Article
                ACA-21-105
                10.4103/aca.ACA_211_17
                5791478
                29336411
                608bcc5d-9e9b-4745-b60c-abe9dcfb3ee4
                Copyright: © 2018 Annals of Cardiac Anaesthesia

                This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

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