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Catastrophic antiphospholipid syndrome in an immune thrombocytopenia patient treated with avatrombopag.

Authors :
Van de Vondel S
Vandenbriele C
Gheysens G
Verhamme P
Janssens A
Source :
Research and practice in thrombosis and haemostasis [Res Pract Thromb Haemost] 2023 Mar 15; Vol. 7 (3), pp. 100125. Date of Electronic Publication: 2023 Mar 15 (Print Publication: 2023).
Publication Year :
2023

Abstract

Background: Avatrombopag is an orally administered second-generation thrombopoietin receptor agonist (TPO-RA) approved for the treatment of chronic immune thrombocytopenia (ITP). However, increased thrombogenicity in patients with ITP after initiation of TPO-RA treatment has been reported.<br />Key Clinical Question: We report a case of a patient with ITP who developed a catastrophic antiphospholipid antibody syndrome (CAPS), following treatment with avatrombopag.<br />Clinical Approach: A20-year-old known chronic patient with ITP presented at the emergency department with a 2-week history of headache, nausea, and abdominal pain, 3 weeks after initiating avatrombopag. In-hospital diagnostic work-up revealed multiple microvascular thrombotic events, including myocardial, cerebrovascular, and pulmonary infarctions. Laboratory test results showed a triple-positive antiphospholipid antibodies serology.<br />Conclusion: The diagnosis of probable avatrombopag-associated CAPS was made.<br /> (© 2023 The Authors.)

Details

Language :
English
ISSN :
2475-0379
Volume :
7
Issue :
3
Database :
MEDLINE
Journal :
Research and practice in thrombosis and haemostasis
Publication Type :
Report
Accession number :
37065845
Full Text :
https://doi.org/10.1016/j.rpth.2023.100125