Catastrophic antiphospholipid syndrome in an immune thrombocytopenia patient treated with avatrombopag

被引:5
|
作者
Van de Vondel, Saartje [1 ]
Vandenbriele, Christophe [2 ]
Gheysens, Gerald [3 ]
Verhamme, Peter [2 ]
Janssens, Ann [1 ]
机构
[1] Katholieke Univ Leuven, Univ Hosp Leuven, Dept Hematol, Leuven, Belgium
[2] Katholieke Univ Leuven, Univ Hosp Leuven, Dept Cardiovasc Sci, Leuven, Belgium
[3] Katholieke Univ Leuven, Univ Hosp Leuven, Dept Radiol, Leuven, Belgium
关键词
ANTIBODIES; MANAGEMENT; DIAGNOSIS; PURPURA;
D O I
10.1016/j.rpth.2023.100125
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.Key Clinical Question: We report a case of a patient with ITP who developed a catastrophic antiphospholipid antibody syndrome (CAPS), following treatment with avatrombopag.Clinical Approach: A 20-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. Conclusion: The diagnosis of probable avatrombopag-associated CAPS was made.
引用
收藏
页数:5
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