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Delirium with delayed diagnosis of hereditary coproporphyria
We present a hereditary coproporphyria patient with acute psychiatric symptoms and skin lesions initially misdiagnosed with schizoaffective disorder and later developed hyperactive delirium and atrial fibrillation requiring intensive care unit admission. He recovered after administering glucose infu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163461/ https://www.ncbi.nlm.nih.gov/pubmed/35662770 http://dx.doi.org/10.1002/ccr3.5937 |
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author | Eroglu, Seyma Birsenogul, Ilhan |
author_facet | Eroglu, Seyma Birsenogul, Ilhan |
author_sort | Eroglu, Seyma |
collection | PubMed |
description | We present a hereditary coproporphyria patient with acute psychiatric symptoms and skin lesions initially misdiagnosed with schizoaffective disorder and later developed hyperactive delirium and atrial fibrillation requiring intensive care unit admission. He recovered after administering glucose infusions and the discontinuation of porphyrinogenic medications. |
format | Online Article Text |
id | pubmed-9163461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91634612022-06-04 Delirium with delayed diagnosis of hereditary coproporphyria Eroglu, Seyma Birsenogul, Ilhan Clin Case Rep Case Reports We present a hereditary coproporphyria patient with acute psychiatric symptoms and skin lesions initially misdiagnosed with schizoaffective disorder and later developed hyperactive delirium and atrial fibrillation requiring intensive care unit admission. He recovered after administering glucose infusions and the discontinuation of porphyrinogenic medications. John Wiley and Sons Inc. 2022-06-02 /pmc/articles/PMC9163461/ /pubmed/35662770 http://dx.doi.org/10.1002/ccr3.5937 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Eroglu, Seyma Birsenogul, Ilhan Delirium with delayed diagnosis of hereditary coproporphyria |
title | Delirium with delayed diagnosis of hereditary coproporphyria |
title_full | Delirium with delayed diagnosis of hereditary coproporphyria |
title_fullStr | Delirium with delayed diagnosis of hereditary coproporphyria |
title_full_unstemmed | Delirium with delayed diagnosis of hereditary coproporphyria |
title_short | Delirium with delayed diagnosis of hereditary coproporphyria |
title_sort | delirium with delayed diagnosis of hereditary coproporphyria |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163461/ https://www.ncbi.nlm.nih.gov/pubmed/35662770 http://dx.doi.org/10.1002/ccr3.5937 |
work_keys_str_mv | AT erogluseyma deliriumwithdelayeddiagnosisofhereditarycoproporphyria AT birsenogulilhan deliriumwithdelayeddiagnosisofhereditarycoproporphyria |