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Korean Journal of Medicine ; : 739-743, 2014.
Artigo em Coreano | WPRIM | ID: wpr-85491

RESUMO

Amyloidosis can be identified by the deposition of amyloid fibrils in biopsy specimens from multiple organs, including the heart, kidney, skin, and bowel. Systemic amyloid protein A amyloidosis (AA amyloidosis) is commonly associated with chronic inflammatory diseases or chronic infectious conditions. Cardiac involvement in AA amyloidosis is found in < 1% of reported cases. Here, we report a case of cardiac AA amyloidosis confirmed by heart biopsy in a 54-year-old-female with a medical history of rheumatoid arthritis and stage 4 chronic kidney disease due to renal amyloidosis. She had suffered from progressive aggravation of dyspnea for 2 years. Infiltrative disease involving the heart was suspected by echocardiography, and the patient was diagnosed with AA amyloidosis involving the heart by cardiac biopsy. This is a rare case of cardiac involvement in a patient with systemic AA amyloidosis associated with rheumatoid arthritis.


Assuntos
Humanos , Amiloide , Amiloidose , Artrite Reumatoide , Biópsia , Dispneia , Ecocardiografia , Insuficiência Cardíaca , Coração , Rim , Insuficiência Renal Crônica , Febre Reumática , Pele , Proteína Estafilocócica A
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