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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...

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Detalles Bibliográficos
Autores principales: Al Hazmi, Ahmed, Winters, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: University of California Irvine, Department of Emergency Medicine publishing Western Journal of Emergency Medicine 2019
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.
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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
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