A giant left atrial myxoma causing left-sided heart failure

Baba, Akiko; Hisata, Yoichi; Odate, Tomohiro; Yamada, Takafumi

doi:10.1177/2050313x221105829

Cited by 2 publications

(2 citation statements)

References 9 publications

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“…Myxoma jantung, meskipun jarang, adalah salah satu tumor jantung primer yang paling umum, kejadiannya sekitar 50% tumor jantung jinak primer. 1,2 Pasien yang menderita myxoma mempunyai rentang usia yang luas (11-82 tahun), 1,3 paling sering pada usia dewasa (rata-rata 50 tahun), dan didominasi wanita. Sembilan puluh persen kasus bersifat sporadis, 10% sisanya terkait dengan sindrom Carney yang umumnya berusia lebih muda (rata-rata 24 tahun) dan biasanya pada laki-laki (66%).…”

Section: Pendahuluanunclassified

Modalitas Pencitraan untuk Diagnosis Myxoma Jantung

Hadiyanti¹

2023

Cermin Dunia Kedokteran

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Myxoma jantung merupakan tumor jantung jinak primer yang paling umum, biasanya ada di atrium kiri dengan titik perlekatan di daerah fossa ovalis. Modalitas pencitraan untuk diagnosis myxoma jantung di antaranya ekokardiografi, computed tomography (CT), magnetic resonance imaging (MRI). Cardiac myxoma is the most common primary benign heart tumor, usually in the left atrium with an attachment point in the fossa ovalis area. Many imaging modalities for cardiac myxoma diagnosis include echocardiography, computed tomography (CT), and magnetic resonance imaging (MRI).

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Section: Pendahuluanunclassified

Modalitas Pencitraan untuk Diagnosis Myxoma Jantung

Hadiyanti¹

2023

Cermin Dunia Kedokteran

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“…Dilation of left atrium (LA) is a factor that prevents the restoration of sinus rhythm and increases the risk of thromboembolic complications [2,5,6,7,8,9]. Joining of giant LA myxoma to this complex pathology further increases the risk of surgery [10,11,12,13,14]. Combination of all the factors determines the feasibility of a comprehensive reconstruction of the left parts of the heart during surgical correction.…”

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Case of Dilated Cardiomyopathy in Combination with Left Atrial Myxoma and Left Atriomegaly (Rare Clinical Case)

Попов

Bolshak

Boukarim

et al. 2022

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Case description. A 41-year-old male patient F. was admitted to the Department ofSurgical Treatment of Ac-quired Heart Diseases of the National Amosov Institute of Cardiovascular Surgery of the National Academy of Medical Sciences of Ukraine with a diagnosis: Dilated cardiomyopathy. Mitral-tricuspid insufϐiciency. Left atrial myxoma. Left atriomegaly. Pulmonary hypertension. The patient was operated with heart failure symptoms of NYHA functional class IV. After a week of medical preparation and additional examination,the patient was successfully operated on (remov-al of the left atrial myxoma, imposition of support rings on the left and right atrioventricular openings, paraanular plicacy of the left atrium). The postoperative period proceededwithout signiϐicant complications. On the 12th day after the operation, the patient was discharged in satisfactorycondition. In the remote period the patient died suddenly 3 years later. Conclusion. Taking into account the initial serious condition of a patient with advanced heart disease with a reduced left ventricular ejection fraction, left atriomegaly (7.8 cm), pulmonary hypertension (50 mm Hg) and comorbidities, complex reconstruction of the left heart in atriomegaly and ventriculomegaly leads to an improvement in the functional state of the myocardium and morphometric indicators of left atrium and left ventricular ejection fraction.

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A giant left atrial myxoma causing left-sided heart failure

Cited by 2 publications

References 9 publications

Modalitas Pencitraan untuk Diagnosis Myxoma Jantung

Modalitas Pencitraan untuk Diagnosis Myxoma Jantung

Case of Dilated Cardiomyopathy in Combination with Left Atrial Myxoma and Left Atriomegaly (Rare Clinical Case)

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