Abstract
Chronic immune thrombocytopenia (ITP) is defined much the same as acute ITP, aside from the duration of thrombocytopenia, which is to exceed 12-month duration, without another identifiable cause. Consideration for underlying etiologies for chronic thrombocytopenia, such as inherited thrombocytopenia disorders, as well as evaluation of secondary causes of ITP, as in immune dysregulation disorders, immunodeficiencies, chronic infections, or autoimmune diseases, should be based on clinical features and family history. In addition to cutaneous bleeding, a clinically significant non-bleeding complaint is fatigue. Treatment options include the same first-line therapies that are utilized in acute ITP, as well as immunomodulatory agents, thrombopoietin receptor agonists (TPO-RA), and in some cases splenectomy.
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Rose, M.J., Jacobson-Kelly, A. (2020). A Preteen Female with Fatigue and Incidental Finding of Thrombocytopenia. In: Dunn, A., Kerlin, B., O'Brien, S., Rose, M., Kumar, R. (eds) Pediatric Bleeding Disorders. Springer, Cham. https://doi.org/10.1007/978-3-030-31661-7_14
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