Light-Chain Cardiac Amyloidosis: A Case Report and Review of the Literature
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Abstract Background: Light-chain (AL) cardiac amyloidosis is a rare cardiomyopathy associated with poor prognosis. Due to the advances of imaging technology, cardiac amyloidosis can be now sufficiently diagnosed without myocardial biopsy. Case presentation: This study reports a 69-year-old female who was admitted with chest distress, abdominal distension, anorexia, resistant hypotension, oliguria, and hyponatremia. The patient was confirmed as AL cardiac amyloidosis with the aid of cardiac MR 2 years after symptom onset. The patient received palliative care due to the end stage of the disease. Conclusions: Early diagnosis by cardiac imaging and etiology-oriented treatment are of importance to improve prognosis of AL cardiac amyloidosis.
2012 ◽
Vol 2012
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pp. 1-3
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2003 ◽
Vol 127
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pp. e371-e373
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2020 ◽
Vol 2
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2017 ◽
Vol 56
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pp. 729-732
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2006 ◽
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pp. 293-295
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1989 ◽
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pp. 186-189
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