Literature DB >> 31587789

Diagnosis and Treatment of Cardiac Amyloidosis Related to Plasma Cell Dyscrasias.

Kevin M Alexander1, Alessandro Evangelisti2, Ronald M Witteles3.   

Abstract

Light chain amyloidosis is a deadly disease in which a monoclonal plasma cell dyscrasia produces misfolded immunoglobulin light chains (AL) that aggregate and form rigid amyloid fibrils. The amyloid deposits infiltrate one or more organs, leading to injury and severe dysfunction. The degree of cardiac involvement is a major driver of morbidity and mortality. Early diagnosis and treatment are crucial to prevent irreversible end-organ damage and improve overall survival. Treatment of AL cardiac amyloidosis involves eliminating the underlying plasma cell dyscrasia with chemotherapy and pursuing supportive heart failure management.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Amyloidosis; Cardiomyopathy; Chemotherapy; Immunoglobulin light chain; Myeloma

Mesh:

Year:  2019        PMID: 31587789     DOI: 10.1016/j.ccl.2019.07.013

Source DB:  PubMed          Journal:  Cardiol Clin        ISSN: 0733-8651            Impact factor:   2.213


  1 in total

1.  Predictors of cardiac involvement and survival in patients with primary systemic light-chain amyloidosis: roles of the clinical, chemical, and 3-D speckle tracking echocardiography parameters.

Authors:  Changhui Lei; Xiaoli Zhu; David H Hsi; Jing Wang; Lei Zuo; Shengjun Ta; Qianli Yang; Lei Xu; Xueli Zhao; Yan Wang; Shiren Sun; Liwen Liu
Journal:  BMC Cardiovasc Disord       Date:  2021-01-21       Impact factor: 2.298

  1 in total

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