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Clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following COVID‐19 vaccination

De novo and relapsed immune‐mediated thrombotic thrombocytopenic purpura (iTTP) have been documented to have occurred following severe acute respiratory syndrome coronavirus 2 (COVID‐19) vaccination. Here, we present a case of a 28‐year‐old woman who received the tozinameran (BNT162b2, Pfizer‐BioNte...

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Autores principales: Deucher, William, Sukumar, Senthil, Cataland, Spero R.
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/PMC8822264/
https://www.ncbi.nlm.nih.gov/pubmed/35155977
http://dx.doi.org/10.1002/rth2.12658
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author Deucher, William
Sukumar, Senthil
Cataland, Spero R.
author_facet Deucher, William
Sukumar, Senthil
Cataland, Spero R.
author_sort Deucher, William
collection PubMed
description De novo and relapsed immune‐mediated thrombotic thrombocytopenic purpura (iTTP) have been documented to have occurred following severe acute respiratory syndrome coronavirus 2 (COVID‐19) vaccination. Here, we present a case of a 28‐year‐old woman who received the tozinameran (BNT162b2, Pfizer‐BioNtech) vaccine for COVID‐19 and experienced an iTTP relapse during longitudinal follow‐up. She received the vaccine 30 months after her initial diagnosis, while she was in clinical remission. She was not in complete ADAMTS‐13 remission, as she had undetectable ADAMTS‐13 activity during follow‐up except for one isolated measurement of 48%. Shortly after vaccination, she developed complaints of bruising, petechiae, ataxia, and an episode of slurred speech. Laboratory testing demonstrated thrombocytopenia, schistocytes, and eventually undetectable ADAMTS‐13 activity. She was successfully treated with caplacizumab, rituximab, and corticosteroids without plasma exchange. She achieved complete clinical and ADAMTS‐13 remission after treatment. We recommend caution in the administration of COVID‐19 vaccines for survivors of iTTP in remission with severely deficient ADAMTS‐13 activity.
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spelling pubmed-88222642022-02-11 Clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following COVID‐19 vaccination Deucher, William Sukumar, Senthil Cataland, Spero R. Res Pract Thromb Haemost Case Report De novo and relapsed immune‐mediated thrombotic thrombocytopenic purpura (iTTP) have been documented to have occurred following severe acute respiratory syndrome coronavirus 2 (COVID‐19) vaccination. Here, we present a case of a 28‐year‐old woman who received the tozinameran (BNT162b2, Pfizer‐BioNtech) vaccine for COVID‐19 and experienced an iTTP relapse during longitudinal follow‐up. She received the vaccine 30 months after her initial diagnosis, while she was in clinical remission. She was not in complete ADAMTS‐13 remission, as she had undetectable ADAMTS‐13 activity during follow‐up except for one isolated measurement of 48%. Shortly after vaccination, she developed complaints of bruising, petechiae, ataxia, and an episode of slurred speech. Laboratory testing demonstrated thrombocytopenia, schistocytes, and eventually undetectable ADAMTS‐13 activity. She was successfully treated with caplacizumab, rituximab, and corticosteroids without plasma exchange. She achieved complete clinical and ADAMTS‐13 remission after treatment. We recommend caution in the administration of COVID‐19 vaccines for survivors of iTTP in remission with severely deficient ADAMTS‐13 activity. John Wiley and Sons Inc. 2022-02-07 /pmc/articles/PMC8822264/ /pubmed/35155977 http://dx.doi.org/10.1002/rth2.12658 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
Deucher, William
Sukumar, Senthil
Cataland, Spero R.
Clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following COVID‐19 vaccination
title Clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following COVID‐19 vaccination
title_full Clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following COVID‐19 vaccination
title_fullStr Clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following COVID‐19 vaccination
title_full_unstemmed Clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following COVID‐19 vaccination
title_short Clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following COVID‐19 vaccination
title_sort clinical relapse of immune‐mediated thrombotic thrombocytopenic purpura following covid‐19 vaccination
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822264/
https://www.ncbi.nlm.nih.gov/pubmed/35155977
http://dx.doi.org/10.1002/rth2.12658
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