What is the definition of Idiopathic Thrombocytopenic Purpura?

Idiopathic thrombocytopenic purpura (ITP) is a bleeding disorder characterized by too few platelets in the blood. This is because platelets are being destroyed by the immune system. Symptoms may include bruising, nosebleed or bleeding in the mouth, bleeding into the skin, and abnormally heavy menstruation. With treatment, the chance of remission (a symptom-free period) is good. Rarely, ITP may become a chronic ailment in adults and reappear, even after remission.

What are the alternative names for Idiopathic Thrombocytopenic Purpura?

  • ITP
  • Autoimmune thrombocytopenic purpura
  • Thrombocytopenic purpura autoimmune
  • Condition: Autoimmune Hemolytic Anemia after BNT162b2 mRNA COVID-19 Vaccination
  • Journal: The Japanese journal of clinical hematology
  • Treatment Used: Oral Prednisolone Therapy
  • Number of Patients: 1
  • Published —
This case report describes a 75-year-old woman who developed autoimmune hemolytic anemia after BNT162b2 mRNA COVID-19 vaccination treated with oral prednisolone.
  • Journal: Frontiers in immunology
  • Published —
Case Report: Autoimmune Psychosis in Chromosome 22q11.2 Deletion Syndrome.