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Extreme Thrombocytosis in Refractory ITP Post-Splenectomy With Associated Fatal Thromboembolism
Author(s) -
Rithin Nedumannil,
Emma Leitinger,
Surender Juneja
Publication year - 2022
Publication title -
clinical pathology
Language(s) - English
Resource type - Journals
ISSN - 2632-010X
DOI - 10.1177/2632010x221083218
Subject(s) - thrombocytosis , thrombopoietin , refractory (planetary science) , medicine , splenectomy , immune thrombocytopenia , thrombopoietin receptor , myeloproliferative neoplasm , agonist , platelet , romiplostim , gastroenterology , immunology , myelofibrosis , receptor , spleen , haematopoiesis , biology , bone marrow , stem cell , astrobiology , genetics
Thrombopoietin (TPO)-receptor agonists have heralded a paradigm shift in the treatment of refractory immune thrombocytopenia (ITP). Reactive thrombocytosis has been described as a secondary effect of such therapies. However, the phenomenon of extreme thrombocytosis with morphology mimicking a myeloproliferative neoplasm (MPN) followed by fatal thromboembolism is unusual in this setting. Caution is required in the diagnosis of refractory ITP as well as TPO-receptor agonist dosing in such cases.

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