Romanian Journal of Internal Medicine (Dec 2019)

Idiopathic thrombocytopenic purpura (ITP) – new era for an old disease

  • Onisâi Minodora,
  • Vlădăreanu Ana-Maria,
  • Spînu Andreea,
  • Găman Mihaela,
  • Bumbea Horia

DOI
https://doi.org/10.2478/rjim-2019-0014
Journal volume & issue
Vol. 57, no. 4
pp. 273 – 283

Abstract

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Immune thrombocytopenia is an autoimmune hematological disorder characterized by severely decreased platelet count of peripheral cause: platelet destruction via antiplatelet antibodies which may also affect marrow megakaryocytes. Patients may present in critical situations, with cutaneous and/or mucous bleeding and possibly life-threatening organ hemorrhages (cerebral, digestive, etc.) Therefore, rapid diagnosis and therapeutic intervention are mandatory.

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