z-logo
open-access-imgOpen Access
Amyloidosis: a unifying diagnosis for nephrotic syndrome and congestive cardiac failure
Author(s) -
Jaskanwal D. Sara,
Ryan B. Khodadadi,
Dylan D Barth,
Mary Caroline Burton
Publication year - 2018
Publication title -
bmj case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.231
H-Index - 26
ISSN - 1757-790X
DOI - 10.1136/bcr-2018-224317
Subject(s) - medicine , nephrotic syndrome , heart failure , amyloidosis , proteinuria , cardiorenal syndrome , cardiology , amyloid (mycology) , fluid restriction , pathology , intensive care medicine , kidney , hyponatremia
Diagnosing patients simply with heart failure or nephrotic syndrome is insufficient, and clinicians should always search for the underlying causes of these syndromes. Amyloidosis represents a rare group of diseases in which abnormal protein, namely amyloid fibrils, build up in various organs. Presentation depends on which organ systems are involved, and symptoms could include breathlessness associated with fluid overload suggestive of cardiac and/or renal involvement and diarrhoea and weight loss, suggestive of gastrointestinal involvement. The authors present a case of congestive cardiac failure and nephrotic range proteinuria in a patient with persistent fluid overload secondary toamyloid light-chain (AL) amyloidosis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here