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An Unusual Presentation of Iron-Deficiency Anemia: An Autobiographical Case Report

Gastroesophageal reflux disease (GERD) is one of the most common gastrointestinal disorders and the use of proton-pump inhibitors has become the mainstay of treatment for many patients. While these are the most effective medications for the management of GERD, there are several side effects that pat...

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Detalles Bibliográficos
Autores principales: Kobets, Andrew, Kobets, Kseniya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760012/
https://www.ncbi.nlm.nih.gov/pubmed/35047279
http://dx.doi.org/10.7759/cureus.20442
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author Kobets, Andrew
Kobets, Kseniya
author_facet Kobets, Andrew
Kobets, Kseniya
author_sort Kobets, Andrew
collection PubMed
description Gastroesophageal reflux disease (GERD) is one of the most common gastrointestinal disorders and the use of proton-pump inhibitors has become the mainstay of treatment for many patients. While these are the most effective medications for the management of GERD, there are several side effects that patients may experience with their use. This autobiographical case report describes the development of iron-deficiency anemia (IdA) with chronic use of omeprazole. The patient was a 35-year-old male with a history of essential hypertension and GERD who was taking omeprazole 40 mg daily for 3 years for the management of reflux symptoms. He developed some mild exercise intolerance and began noticing an affinity for unusual smells, including gasoline and dust, which prompted an evaluation. Lab work demonstrated IdA to 8.3 g/dl, which was not corrected by oral iron supplementation. Sources of gastrointestinal bleeding, Helicobacter pylori infection, and other hypersecretion syndromes were ruled out. IV iron response was transient and only after 8 months of discontinuation of omeprazole did the anemia correct on its own. Omeprazole has increasingly become recognized as a cause of IdA, but only three clinical case reports have been documented in the literature. At least two mechanisms may be involved, and the discontinuation of omeprazole may correct the anemia in 2 months in mild cases, but up to 8 months in more severe cases. The presence of an abnormal propensity for unusual smells, similar to pica as seen in other IdAs, was a unique feature of this case and should prompt evaluation.
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spelling pubmed-87600122022-01-18 An Unusual Presentation of Iron-Deficiency Anemia: An Autobiographical Case Report Kobets, Andrew Kobets, Kseniya Cureus Family/General Practice Gastroesophageal reflux disease (GERD) is one of the most common gastrointestinal disorders and the use of proton-pump inhibitors has become the mainstay of treatment for many patients. While these are the most effective medications for the management of GERD, there are several side effects that patients may experience with their use. This autobiographical case report describes the development of iron-deficiency anemia (IdA) with chronic use of omeprazole. The patient was a 35-year-old male with a history of essential hypertension and GERD who was taking omeprazole 40 mg daily for 3 years for the management of reflux symptoms. He developed some mild exercise intolerance and began noticing an affinity for unusual smells, including gasoline and dust, which prompted an evaluation. Lab work demonstrated IdA to 8.3 g/dl, which was not corrected by oral iron supplementation. Sources of gastrointestinal bleeding, Helicobacter pylori infection, and other hypersecretion syndromes were ruled out. IV iron response was transient and only after 8 months of discontinuation of omeprazole did the anemia correct on its own. Omeprazole has increasingly become recognized as a cause of IdA, but only three clinical case reports have been documented in the literature. At least two mechanisms may be involved, and the discontinuation of omeprazole may correct the anemia in 2 months in mild cases, but up to 8 months in more severe cases. The presence of an abnormal propensity for unusual smells, similar to pica as seen in other IdAs, was a unique feature of this case and should prompt evaluation. Cureus 2021-12-15 /pmc/articles/PMC8760012/ /pubmed/35047279 http://dx.doi.org/10.7759/cureus.20442 Text en Copyright © 2021, Kobets et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Family/General Practice
Kobets, Andrew
Kobets, Kseniya
An Unusual Presentation of Iron-Deficiency Anemia: An Autobiographical Case Report
title An Unusual Presentation of Iron-Deficiency Anemia: An Autobiographical Case Report
title_full An Unusual Presentation of Iron-Deficiency Anemia: An Autobiographical Case Report
title_fullStr An Unusual Presentation of Iron-Deficiency Anemia: An Autobiographical Case Report
title_full_unstemmed An Unusual Presentation of Iron-Deficiency Anemia: An Autobiographical Case Report
title_short An Unusual Presentation of Iron-Deficiency Anemia: An Autobiographical Case Report
title_sort unusual presentation of iron-deficiency anemia: an autobiographical case report
topic Family/General Practice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760012/
https://www.ncbi.nlm.nih.gov/pubmed/35047279
http://dx.doi.org/10.7759/cureus.20442
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