Journal of Clinical and Diagnostic Research (Apr 2017)

Cardiac Amyloidosis, An Infiltrative Heart Disease Presenting as Arrhythmia-A Case Report

  • B Magesh,
  • Deepak Kadeli,
  • Sunil Bohra,
  • V Krishnaprasath,
  • R Keshava

DOI
https://doi.org/10.7860/JCDR/2017/24698.9661
Journal volume & issue
Vol. 11, no. 4
pp. OD14 – OD15

Abstract

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Cardiac amyloidosis is a manifestation of amyloidosis which is a multisystem disorder. This is difficult to diagnose, rare disease which eventually leads to the mortality. Diagnosis requires a high index of clinical suspicion along with echocardiographic clues like, diastolic dysfunction, bi-atrial enlargement and ventricular thickening. Treatment is mainly supportive with disappointing outcomes. We present a case of systemic amyloidosis with negative congo red staining, presenting with predominantly cardiac features.

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