Complicated Long Term Vaccine Induced Thrombotic Immune Thrombocytopenia—A Case Report

Background and Objectives: Vaccine induced thrombotic thrombocytopenia (VITT) may occur after COVID-19 vaccination with recombinant adenoviral vector-based vaccines. VITT can present as cerebral sinus and venous thrombosis (CSVT), often complicated by intracranial hemorrhage. Today it is unclear, ho...

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Autores principales: Albrecht Günther, Dirk Brämer, Mathias W. Pletz, Thomas Kamradt, Sabine Baumgart, Thomas E. Mayer, Michael Baier, Angelina Autsch, Christian Mawrin, Linda Schönborn, Andreas Greinacher, Thomas Thiele
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:61ada4457095468f9fce453292077d0e2021-11-25T19:11:29ZComplicated Long Term Vaccine Induced Thrombotic Immune Thrombocytopenia—A Case Report10.3390/vaccines91113442076-393Xhttps://doaj.org/article/61ada4457095468f9fce453292077d0e2021-11-01T00:00:00Zhttps://www.mdpi.com/2076-393X/9/11/1344https://doaj.org/toc/2076-393XBackground and Objectives: Vaccine induced thrombotic thrombocytopenia (VITT) may occur after COVID-19 vaccination with recombinant adenoviral vector-based vaccines. VITT can present as cerebral sinus and venous thrombosis (CSVT), often complicated by intracranial hemorrhage. Today it is unclear, how long symptomatic VITT can persist. Here, we report the complicated long-term course of a VITT patient with extremely high titers of pathogenic anti-platelet factor 4 (PF4)-IgG antibodies. Methods: Clinical and laboratory findings are presented, including the course of platelet counts, D-Dimer levels, clinical presentation, imaging, SARS-CoV-2-serological and immunological, platelet activating anti-PF4-IgG, as well as autopsy findings. Results: The patient presented with extended superior sagittal sinus thrombosis with accompanying bifrontal intracerebral hemorrhage. Repeated treatment with intravenous immune globuline (IVIG) resolved recurrent episodes of thrombocytopenia. Moreover, the patient’s serum remained strongly positive for platelet-activating anti-PF4-IgG over three months. After a period of clinical stabilization, the patient suffered a recurrent and fatal intracranial hemorrhage. Conclusions: Complicated VITT with extremely high anti-PF4-IgG titers over three months can induce recurrent thrombocytopenia despite treatment with IVIG and anticoagulation. Plasma exchange, immunoadsorption, and /or immunosuppressive treatment may be considered in complicated VITT to reduce extraordinarily high levels of anti-PF4-IgG. Long-term therapy in such cases must take the individual bleeding risk and CSVT risk into account.Albrecht GüntherDirk BrämerMathias W. PletzThomas KamradtSabine BaumgartThomas E. MayerMichael BaierAngelina AutschChristian MawrinLinda SchönbornAndreas GreinacherThomas ThieleMDPI AGarticlevaccineCOVID-19thrombocytopeniacerebral thrombosisautoimmunecase reportMedicineRENVaccines, Vol 9, Iss 1344, p 1344 (2021)
institution DOAJ
collection DOAJ
language EN
topic vaccine
COVID-19
thrombocytopenia
cerebral thrombosis
autoimmune
case report
Medicine
R
spellingShingle vaccine
COVID-19
thrombocytopenia
cerebral thrombosis
autoimmune
case report
Medicine
R
Albrecht Günther
Dirk Brämer
Mathias W. Pletz
Thomas Kamradt
Sabine Baumgart
Thomas E. Mayer
Michael Baier
Angelina Autsch
Christian Mawrin
Linda Schönborn
Andreas Greinacher
Thomas Thiele
Complicated Long Term Vaccine Induced Thrombotic Immune Thrombocytopenia—A Case Report
description Background and Objectives: Vaccine induced thrombotic thrombocytopenia (VITT) may occur after COVID-19 vaccination with recombinant adenoviral vector-based vaccines. VITT can present as cerebral sinus and venous thrombosis (CSVT), often complicated by intracranial hemorrhage. Today it is unclear, how long symptomatic VITT can persist. Here, we report the complicated long-term course of a VITT patient with extremely high titers of pathogenic anti-platelet factor 4 (PF4)-IgG antibodies. Methods: Clinical and laboratory findings are presented, including the course of platelet counts, D-Dimer levels, clinical presentation, imaging, SARS-CoV-2-serological and immunological, platelet activating anti-PF4-IgG, as well as autopsy findings. Results: The patient presented with extended superior sagittal sinus thrombosis with accompanying bifrontal intracerebral hemorrhage. Repeated treatment with intravenous immune globuline (IVIG) resolved recurrent episodes of thrombocytopenia. Moreover, the patient’s serum remained strongly positive for platelet-activating anti-PF4-IgG over three months. After a period of clinical stabilization, the patient suffered a recurrent and fatal intracranial hemorrhage. Conclusions: Complicated VITT with extremely high anti-PF4-IgG titers over three months can induce recurrent thrombocytopenia despite treatment with IVIG and anticoagulation. Plasma exchange, immunoadsorption, and /or immunosuppressive treatment may be considered in complicated VITT to reduce extraordinarily high levels of anti-PF4-IgG. Long-term therapy in such cases must take the individual bleeding risk and CSVT risk into account.
format article
author Albrecht Günther
Dirk Brämer
Mathias W. Pletz
Thomas Kamradt
Sabine Baumgart
Thomas E. Mayer
Michael Baier
Angelina Autsch
Christian Mawrin
Linda Schönborn
Andreas Greinacher
Thomas Thiele
author_facet Albrecht Günther
Dirk Brämer
Mathias W. Pletz
Thomas Kamradt
Sabine Baumgart
Thomas E. Mayer
Michael Baier
Angelina Autsch
Christian Mawrin
Linda Schönborn
Andreas Greinacher
Thomas Thiele
author_sort Albrecht Günther
title Complicated Long Term Vaccine Induced Thrombotic Immune Thrombocytopenia—A Case Report
title_short Complicated Long Term Vaccine Induced Thrombotic Immune Thrombocytopenia—A Case Report
title_full Complicated Long Term Vaccine Induced Thrombotic Immune Thrombocytopenia—A Case Report
title_fullStr Complicated Long Term Vaccine Induced Thrombotic Immune Thrombocytopenia—A Case Report
title_full_unstemmed Complicated Long Term Vaccine Induced Thrombotic Immune Thrombocytopenia—A Case Report
title_sort complicated long term vaccine induced thrombotic immune thrombocytopenia—a case report
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/61ada4457095468f9fce453292077d0e
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