Frontiers in Immunology (Apr 2025)

Case Report: A case of pediatric persistent refractory ITP responsive to avatrombopag

  • Antonella Sau,
  • Gianfranco Di Prinzio,
  • Daniela Onofrillo,
  • Anna Caterina Russo,
  • Nicole Santoro,
  • Mauro Di Ianni

DOI
https://doi.org/10.3389/fimmu.2025.1576053
Journal volume & issue
Vol. 16

Abstract

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Immune thrombocytopenia (ITP) is a rare hematologic disorder characterized by low platelet counts due to an immune-mediated destruction of platelets. While corticosteroids, intravenous immunoglobulin (IVIG) are the mainstays of treatment, a subset of patients may remain refractory to these therapies. Here, we present a case of a 6-year-old girl diagnosed with refractory ITP, who failed to respond to standard therapies but showed a remarkable clinical improvement with avatrombopag, a thrombopoietin receptor agonist.

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