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Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report
BACKGROUND: The presentation of idiopathic intracranial hypertension (IIH) in association with iron deficiency anemia (IDA) is rare. CASE PRESENTATION: This case report depicts the unusual case of a 31-year-old woman of mixed Jamaican and English heritage with IIH who presented initially as IDA in t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852283/ https://www.ncbi.nlm.nih.gov/pubmed/33526092 http://dx.doi.org/10.1186/s13256-020-02631-2 |
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author | Sim, Peng Yong Taribagil, Priyal Woollacott, Ione O. C. Rashid, Safina Kidd, Desmond P. |
author_facet | Sim, Peng Yong Taribagil, Priyal Woollacott, Ione O. C. Rashid, Safina Kidd, Desmond P. |
author_sort | Sim, Peng Yong |
collection | PubMed |
description | BACKGROUND: The presentation of idiopathic intracranial hypertension (IIH) in association with iron deficiency anemia (IDA) is rare. CASE PRESENTATION: This case report depicts the unusual case of a 31-year-old woman of mixed Jamaican and English heritage with IIH who presented initially as IDA in the context of menorrhagia. Subsequent ophthalmic review, lumbar puncture, cerebrospinal fluid analysis and neuroimaging studies revealed severe bilateral optic disc swelling and raised intracranial pressure in keeping with IIH. Prompt treatment of IDA with blood transfusion and orally administered iron supplements, in addition to medical treatment for IIH, contributed to significant improvement of symptoms and prevented long-term visual deficits. CONCLUSION: The possibility of IDA, albeit rare, should always be considered and investigated appropriately in all patients with IIH, as the treatment of the anemia alone may be sight-saving. |
format | Online Article Text |
id | pubmed-7852283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78522832021-02-04 Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report Sim, Peng Yong Taribagil, Priyal Woollacott, Ione O. C. Rashid, Safina Kidd, Desmond P. J Med Case Rep Case Report BACKGROUND: The presentation of idiopathic intracranial hypertension (IIH) in association with iron deficiency anemia (IDA) is rare. CASE PRESENTATION: This case report depicts the unusual case of a 31-year-old woman of mixed Jamaican and English heritage with IIH who presented initially as IDA in the context of menorrhagia. Subsequent ophthalmic review, lumbar puncture, cerebrospinal fluid analysis and neuroimaging studies revealed severe bilateral optic disc swelling and raised intracranial pressure in keeping with IIH. Prompt treatment of IDA with blood transfusion and orally administered iron supplements, in addition to medical treatment for IIH, contributed to significant improvement of symptoms and prevented long-term visual deficits. CONCLUSION: The possibility of IDA, albeit rare, should always be considered and investigated appropriately in all patients with IIH, as the treatment of the anemia alone may be sight-saving. BioMed Central 2021-02-02 /pmc/articles/PMC7852283/ /pubmed/33526092 http://dx.doi.org/10.1186/s13256-020-02631-2 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Sim, Peng Yong Taribagil, Priyal Woollacott, Ione O. C. Rashid, Safina Kidd, Desmond P. Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report |
title | Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report |
title_full | Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report |
title_fullStr | Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report |
title_full_unstemmed | Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report |
title_short | Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report |
title_sort | idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852283/ https://www.ncbi.nlm.nih.gov/pubmed/33526092 http://dx.doi.org/10.1186/s13256-020-02631-2 |
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