Cargando…
Acquired hemophilia following COVID‐19 vaccination: Case report and review of literature
BACKGROUND: Acquired hemophilia A (AHA) is a rare bleeding disorder that can lead to spontaneous hemorrhage or bleeding induced by invasive procedures or trauma. We describe a patient who presented with multiple hematomas and a relapse of bullous pemphigoid shortly after his first dose of Vaxzevria...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459413/ https://www.ncbi.nlm.nih.gov/pubmed/36176309 http://dx.doi.org/10.1002/rth2.12785 |
_version_ | 1784786503713423360 |
---|---|
author | Happaerts, Michiel Vanassche, Thomas |
author_facet | Happaerts, Michiel Vanassche, Thomas |
author_sort | Happaerts, Michiel |
collection | PubMed |
description | BACKGROUND: Acquired hemophilia A (AHA) is a rare bleeding disorder that can lead to spontaneous hemorrhage or bleeding induced by invasive procedures or trauma. We describe a patient who presented with multiple hematomas and a relapse of bullous pemphigoid shortly after his first dose of Vaxzevria ChAdOx1‐S COVID‐19 vaccination. We reviewed literature for cases of AHA following COVID‐19 vaccination. KEY CLINICAL QUESTION: Can COVID‐19 vaccines induce (a recurrence of) AHA? CLINICAL APPROACH AND CONCLUSIONS: The diagnosis of AHA with a relapse of bullous pemphigoid was made. The patient was treated with recombinant activated factor VII, emicizumab, rituximab, and methylprednisolone. There were no further bleeding events. However, the patient deteriorated because of sepsis and died on the fifteenth day of admission. CONCLUSION: Vaccines may trigger autoimmune events such as AHA. However, proof of causality is not possible and in this case the relapse of bullous pemphigoid before vaccination challenges this even more. |
format | Online Article Text |
id | pubmed-9459413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94594132022-09-28 Acquired hemophilia following COVID‐19 vaccination: Case report and review of literature Happaerts, Michiel Vanassche, Thomas Res Pract Thromb Haemost Case Report BACKGROUND: Acquired hemophilia A (AHA) is a rare bleeding disorder that can lead to spontaneous hemorrhage or bleeding induced by invasive procedures or trauma. We describe a patient who presented with multiple hematomas and a relapse of bullous pemphigoid shortly after his first dose of Vaxzevria ChAdOx1‐S COVID‐19 vaccination. We reviewed literature for cases of AHA following COVID‐19 vaccination. KEY CLINICAL QUESTION: Can COVID‐19 vaccines induce (a recurrence of) AHA? CLINICAL APPROACH AND CONCLUSIONS: The diagnosis of AHA with a relapse of bullous pemphigoid was made. The patient was treated with recombinant activated factor VII, emicizumab, rituximab, and methylprednisolone. There were no further bleeding events. However, the patient deteriorated because of sepsis and died on the fifteenth day of admission. CONCLUSION: Vaccines may trigger autoimmune events such as AHA. However, proof of causality is not possible and in this case the relapse of bullous pemphigoid before vaccination challenges this even more. John Wiley and Sons Inc. 2022-09-09 /pmc/articles/PMC9459413/ /pubmed/36176309 http://dx.doi.org/10.1002/rth2.12785 Text en © 2022 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH). 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 Report Happaerts, Michiel Vanassche, Thomas Acquired hemophilia following COVID‐19 vaccination: Case report and review of literature |
title | Acquired hemophilia following COVID‐19 vaccination: Case report and review of literature |
title_full | Acquired hemophilia following COVID‐19 vaccination: Case report and review of literature |
title_fullStr | Acquired hemophilia following COVID‐19 vaccination: Case report and review of literature |
title_full_unstemmed | Acquired hemophilia following COVID‐19 vaccination: Case report and review of literature |
title_short | Acquired hemophilia following COVID‐19 vaccination: Case report and review of literature |
title_sort | acquired hemophilia following covid‐19 vaccination: case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459413/ https://www.ncbi.nlm.nih.gov/pubmed/36176309 http://dx.doi.org/10.1002/rth2.12785 |
work_keys_str_mv | AT happaertsmichiel acquiredhemophiliafollowingcovid19vaccinationcasereportandreviewofliterature AT vanasschethomas acquiredhemophiliafollowingcovid19vaccinationcasereportandreviewofliterature |