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Reversible Cerebral Vasoconstriction Syndrome due to Atovaquone
A 72-year-old Japanese woman with rheumatoid arthritis whose activity decreased with previous treatments had recurrent thunderclap headaches during an atovaquone regimen for the treatment of pneumocystis pneumonia. The recurrent headaches disappeared after discontinuation of the drug. Brain magnetic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803701/ https://www.ncbi.nlm.nih.gov/pubmed/29422854 http://dx.doi.org/10.1159/000484551 |
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author | Makino, Takahiro Kamitsukasa, Ikuo Ito, Shoichi |
author_facet | Makino, Takahiro Kamitsukasa, Ikuo Ito, Shoichi |
author_sort | Makino, Takahiro |
collection | PubMed |
description | A 72-year-old Japanese woman with rheumatoid arthritis whose activity decreased with previous treatments had recurrent thunderclap headaches during an atovaquone regimen for the treatment of pneumocystis pneumonia. The recurrent headaches disappeared after discontinuation of the drug. Brain magnetic resonance images showed multiple cerebral vasoconstrictions of cerebral arteries with vasogenic cerebral white matter edema, which diminished several weeks later. We diagnosed the patient's headaches as reversible cerebral vasoconstriction syndrome due to atovaquone. |
format | Online Article Text |
id | pubmed-5803701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-58037012018-02-08 Reversible Cerebral Vasoconstriction Syndrome due to Atovaquone Makino, Takahiro Kamitsukasa, Ikuo Ito, Shoichi Case Rep Neurol Case Report A 72-year-old Japanese woman with rheumatoid arthritis whose activity decreased with previous treatments had recurrent thunderclap headaches during an atovaquone regimen for the treatment of pneumocystis pneumonia. The recurrent headaches disappeared after discontinuation of the drug. Brain magnetic resonance images showed multiple cerebral vasoconstrictions of cerebral arteries with vasogenic cerebral white matter edema, which diminished several weeks later. We diagnosed the patient's headaches as reversible cerebral vasoconstriction syndrome due to atovaquone. S. Karger AG 2017-12-19 /pmc/articles/PMC5803701/ /pubmed/29422854 http://dx.doi.org/10.1159/000484551 Text en Copyright © 2017 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Case Report Makino, Takahiro Kamitsukasa, Ikuo Ito, Shoichi Reversible Cerebral Vasoconstriction Syndrome due to Atovaquone |
title | Reversible Cerebral Vasoconstriction Syndrome due to Atovaquone |
title_full | Reversible Cerebral Vasoconstriction Syndrome due to Atovaquone |
title_fullStr | Reversible Cerebral Vasoconstriction Syndrome due to Atovaquone |
title_full_unstemmed | Reversible Cerebral Vasoconstriction Syndrome due to Atovaquone |
title_short | Reversible Cerebral Vasoconstriction Syndrome due to Atovaquone |
title_sort | reversible cerebral vasoconstriction syndrome due to atovaquone |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803701/ https://www.ncbi.nlm.nih.gov/pubmed/29422854 http://dx.doi.org/10.1159/000484551 |
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