Hamostaseologie 2023; 43(03): 215-218
DOI: 10.1055/a-1497-1054
Case Report

COVID-19 as a Potential Trigger for Immune Thrombotic Thrombocytopenic Purpura and Reason for an Unusual Treatment: A Case Report

Marie-Kristin Schwaegermann
1   Department of Internal Medicine III, Comprehensive Cancer Center, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Lukas Hobohm
2   Department of Cardiology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
3   Centre of Thrombosis and Hemostasis (CTH), University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Johanna Rausch
1   Department of Internal Medicine III, Comprehensive Cancer Center, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Michael Reuter
4   Department of Internal Medicine I, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Thomas-Friedrich Griemert
4   Department of Internal Medicine I, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Visvakanth Sivanathan
4   Department of Internal Medicine I, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Tanja Falter
5   Institute of Laboratory Medicine and Clinical Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Martin F. Sprinzl
4   Department of Internal Medicine I, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
5   Institute of Laboratory Medicine and Clinical Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Karl J. Lackner
5   Institute of Laboratory Medicine and Clinical Chemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Peter R. Galle
4   Department of Internal Medicine I, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Stavros Konstantinides
3   Centre of Thrombosis and Hemostasis (CTH), University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Matthias Theobald
1   Department of Internal Medicine III, Comprehensive Cancer Center, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
,
Charis von Auer
1   Department of Internal Medicine III, Comprehensive Cancer Center, University Medical Center of the Johannes Gutenberg University, Mainz, Germany
3   Centre of Thrombosis and Hemostasis (CTH), University Medical Center of the Johannes Gutenberg University, Mainz, Germany
› Author Affiliations
Funding Not applicable.

Abstract

Immune thrombotic thrombocytopenic purpura (iTTP) is a rare autoimmune disorder characterized by severely reduced activity of the von Willebrand factor (VWF)-cleaving protease ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) due to autoantibodies. This leads to the development of pathogenic multimers of VWF, causing a thrombotic microangiopathy with decreased number of platelets, hemolysis, and life-threatening tissue ischemia of mostly brain, heart, and kidneys. Standard treatment of iTTP involves daily plasma exchange to remove ultra large multimers of VWF, inhibitors, substituting ADAMTS13, and the accompaniment of an immunosuppressive treatment with steroids. Recently, caplacizumab was approved for iTTP. Caplacizumab is a nanobody binding the A1 domain of VWF, blocking its interaction with glycoprotein Ib–IX–V platelet receptor and therefore preventing platelet aggregation. VWF activities may serve as therapeutic drug monitoring of caplacizumab, whereas ADAMTS13 activities may be used for biomarkers to guide caplacizumab treatment modalities and overall treatment duration. Additional immunosuppressive treatment by inhibiting autoantibody formation (e.g., the use of Rituximab, a chimeric monoclonal antibody directed against the B-cell antigen CD20) is a further treatment option. Infections are well-known causes for an acute episode for patients with iTTP. The novel SARS-CoV-2 virus is mainly associated with acute respiratory distress as well as diffuse endothelial inflammation and increased coagulopathy. However, little is known about an infection with SARS-CoV-2 virus triggering iTTP relapses. We herein report the case of an acute iTTP episode accompanying a SARS-CoV-2 infection.

Competing Interests

The authors have no competing interests.


Ethics Approval

Not applicable.


Consent to Participate

Informed consent was obtained from all individual participants included.


Author Contributions

All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by Marie-Kristin Schwaegermann and Charis von Auer. The first draft of the manuscript was written by Marie-Kristin Schwaegermann and amended by Charis von Auer. Lukas Hobohm prepared the diagram for laboratory results. All authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.




Publication History

Received: 16 March 2021

Accepted: 01 May 2021

Article published online:
29 July 2021

© 2021. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
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