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A 62-year-old man was admitted to our hospital for the control of heart failure and pneumonia (figure 1A). His medical history included chronic atrial fibrillation for 20 years and the presence of a large left atrium (LA) without a family history of heart disease. Echocardiography showed a huge LA, a normal range of diastolic wall thickness of 9 mm, a 56% ejection fraction, a mean E/e′ of 8 and mild mitral regurgitation without stenosis (figure 1B). A CT image (figure 1C) showed a giant LA (16.4×12.9×15.7cm). After the control of infection (figure 1D), cardiac catheterisation revealed a high pulmonary capillary wedged pressure (mean of 29 mm Hg) and an end-diastolic left ventricular pressure (22mm Hg) without a dip and plateau pattern showing that he had restrictive cardiomyopathy. One year later, he died due to heart failure. The weight of the heart was increased up to 490 g with a markedly enlarged LA in an autopsy. Microscopic examination revealed unexpectedly hypertrophic cardiomyopathy with disarrayed cardiomyocytes (figure 2A: H&E staining), patty fibrosis (figure 2B: Azan staining), and normal pathology of atrium and mitral valve. This giant LA is the second largest one and the first autopsy case ever reported to our knowledge,1 implicating the extensibility of LA in compensation of restrictive left ventricle. LA volume was reported to be a powerful predictor of mortality in heart diseases and markedly increased by mitral valve diseases and a restrictive left ventricle, such as hypertension, dilated cardiomyopathy, hypertrophic cardiomyopathy, restrictive cardiomyopathy and amyloidosis.2
Footnotes
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Contributors TK analysed and interpreted the data, drafted the manuscript, and provided critical revision of the manuscript for important intellectual content. TF acquired the data. MI supervised.
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Competing interests None.
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Patient consent Obtained.
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Provenance and peer review Not commissioned; internally peer reviewed.