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CASE REPORT
Acute cardiac tamponade in light-chain amyloidosis
  1. Mikhail Kuprian1,
  2. George Mount2
  1. 1Madigan Army Medical Center, Tacoma, Washington, USA
  2. 2Department of Rheumatology, Madigan Army Medical Center, Tacoma, Washington, USA
  1. Correspondence to Dr Mikhail Kuprian, mike.kuprian{at}gmail.com

Summary

A 71-year-old woman, with a history of light-chain amyloidosis, presented with a sudden onset dyspnoea. Echocardiography showed a large pericardial effusion with compression of the right atrium and the right ventricle. Right heart catheterisation demonstrated equalisation of her diastolic pressures consistent with cardiac tamponade. Pericardiocentesis revealed a haemmorrhagic exudative effusion with no evidence of malignancy. Bone marrow biopsy and other investigations showed no evidence of multiple myeloma. Her effusion recurred 2 weeks later and repeat pericardiocentesis demonstrated similar findings. She was started on chemotherapy with no further recurrence of pericardial effusion. The patient was unable to tolerate chemotherapy and died 1 year after initial presentation. This case represents a rare manifestation of cardiac amyloidosis and explores the reported aetiologies for cardiac tamponade in the setting of light-chain amyloidosis. Acute and definitive treatments are also discussed.

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