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Evans Syndrome
A 22-year-old man presented to the emergency department with facial swelling, rash, and fatigue. He had a past medical history of pericarditis and pericardial effusion. His evaluation showed anemia and thrombocytopenia. He was admitted for intravenous administration of steroids, plasmapheresis, and...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497206/ https://www.ncbi.nlm.nih.gov/pubmed/31061968 http://dx.doi.org/10.5811/cpcem.2019.1.41028 |
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author | Al Hazmi, Ahmed Winters, Michael E. |
author_facet | Al Hazmi, Ahmed Winters, Michael E. |
author_sort | Al Hazmi, Ahmed |
collection | PubMed |
description | A 22-year-old man presented to the emergency department with facial swelling, rash, and fatigue. He had a past medical history of pericarditis and pericardial effusion. His evaluation showed anemia and thrombocytopenia. He was admitted for intravenous administration of steroids, plasmapheresis, and workup of his anemia and thrombocytopenia. He was ultimately diagnosed with Evans syndrome as a presenting feature of systemic lupus erythematosus. Plasmapheresis was stopped but administration of steroids continued. His blood counts improved, and the facial swelling and rash subsided. Evans syndrome is an immunologic conundrum that requires early recognition and treatment. |
format | Online Article Text |
id | pubmed-6497206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-64972062019-05-06 Evans Syndrome Al Hazmi, Ahmed Winters, Michael E. Clin Pract Cases Emerg Med Case Report A 22-year-old man presented to the emergency department with facial swelling, rash, and fatigue. He had a past medical history of pericarditis and pericardial effusion. His evaluation showed anemia and thrombocytopenia. He was admitted for intravenous administration of steroids, plasmapheresis, and workup of his anemia and thrombocytopenia. He was ultimately diagnosed with Evans syndrome as a presenting feature of systemic lupus erythematosus. Plasmapheresis was stopped but administration of steroids continued. His blood counts improved, and the facial swelling and rash subsided. Evans syndrome is an immunologic conundrum that requires early recognition and treatment. University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine 2019-02-26 /pmc/articles/PMC6497206/ /pubmed/31061968 http://dx.doi.org/10.5811/cpcem.2019.1.41028 Text en Copyright: © 2019 Hazmi et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) License. See: http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Case Report Al Hazmi, Ahmed Winters, Michael E. Evans Syndrome |
title | Evans Syndrome |
title_full | Evans Syndrome |
title_fullStr | Evans Syndrome |
title_full_unstemmed | Evans Syndrome |
title_short | Evans Syndrome |
title_sort | evans syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497206/ https://www.ncbi.nlm.nih.gov/pubmed/31061968 http://dx.doi.org/10.5811/cpcem.2019.1.41028 |
work_keys_str_mv | AT alhazmiahmed evanssyndrome AT wintersmichaele evanssyndrome |