Deferasirox – a rarer cause of Fanconi syndrome

Deferasirox is a recently approved iron chelator and is widely used to treat iron overload in transfusion-dependent patients. Its once-daily dosing and oral route of administration have made it an appealing alternative to deferoxamine. Recent case studies have brought to light its potential to cause...

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Main Authors: Iman Khan, Mustafa Muhammad, Janki Patel
Format: Article
Language:English
Published: Greater Baltimore Medical Center 2019-07-01
Series:Journal of Community Hospital Internal Medicine Perspectives
Subjects:
Online Access:http://dx.doi.org/10.1080/20009666.2019.1650592
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author Iman Khan
Mustafa Muhammad
Janki Patel
author_facet Iman Khan
Mustafa Muhammad
Janki Patel
author_sort Iman Khan
collection DOAJ
description Deferasirox is a recently approved iron chelator and is widely used to treat iron overload in transfusion-dependent patients. Its once-daily dosing and oral route of administration have made it an appealing alternative to deferoxamine. Recent case studies have brought to light its potential to cause damage to the proximal convoluted tubule resulting in Fanconi syndrome (FS). FS is a proximal tubular dysfunction that leads to glycosuria, phosphaturia, aminoaciduria, and normal anion gap metabolic acidosis. Herein, we discuss a case of a young male on chronic blood transfusions requiring deferasirox therapy, who was found to have FS from its use. We discuss the possible mechanism of drug toxicity and the need for regular monitoring of serum electrolytes andurinalysis along with renal function tests to avoid this consequence.
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spelling doaj.art-de0784367f164553b23cbae810a704472023-01-03T02:35:42ZengGreater Baltimore Medical CenterJournal of Community Hospital Internal Medicine Perspectives2000-96662019-07-019435835910.1080/20009666.2019.16505921650592Deferasirox – a rarer cause of Fanconi syndromeIman Khan0Mustafa Muhammad1Janki Patel2Greater Baltimore Medical CenterGreater Baltimore Medical CenterGreater Baltimore Medical CenterDeferasirox is a recently approved iron chelator and is widely used to treat iron overload in transfusion-dependent patients. Its once-daily dosing and oral route of administration have made it an appealing alternative to deferoxamine. Recent case studies have brought to light its potential to cause damage to the proximal convoluted tubule resulting in Fanconi syndrome (FS). FS is a proximal tubular dysfunction that leads to glycosuria, phosphaturia, aminoaciduria, and normal anion gap metabolic acidosis. Herein, we discuss a case of a young male on chronic blood transfusions requiring deferasirox therapy, who was found to have FS from its use. We discuss the possible mechanism of drug toxicity and the need for regular monitoring of serum electrolytes andurinalysis along with renal function tests to avoid this consequence.http://dx.doi.org/10.1080/20009666.2019.1650592NephropathyelectrolytesFanconiproximal
spellingShingle Iman Khan
Mustafa Muhammad
Janki Patel
Deferasirox – a rarer cause of Fanconi syndrome
Journal of Community Hospital Internal Medicine Perspectives
Nephropathy
electrolytes
Fanconi
proximal
title Deferasirox – a rarer cause of Fanconi syndrome
title_full Deferasirox – a rarer cause of Fanconi syndrome
title_fullStr Deferasirox – a rarer cause of Fanconi syndrome
title_full_unstemmed Deferasirox – a rarer cause of Fanconi syndrome
title_short Deferasirox – a rarer cause of Fanconi syndrome
title_sort deferasirox a rarer cause of fanconi syndrome
topic Nephropathy
electrolytes
Fanconi
proximal
url http://dx.doi.org/10.1080/20009666.2019.1650592
work_keys_str_mv AT imankhan deferasiroxararercauseoffanconisyndrome
AT mustafamuhammad deferasiroxararercauseoffanconisyndrome
AT jankipatel deferasiroxararercauseoffanconisyndrome