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Idiopathic Thrombocytopaenic Purpura

Idiopathic Thrombocytopaenic Purpura

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Pathology:

Antibody mediated destruction of megakaryocytes and platelets is the primary pathology of this condition.

Aetiology:

The exact cause of this pathology is largely unknown, though it is often preceded by a viral infection in children.

Symptoms:

  • Easy bruising
  • Menorrhagia (abnormally heavy menstrual bleeding)
  • Epistaxis (nosebleed)
  • Prolonged bleeding

Signs:

Purpura (spontaneous discoloration of the skin caused by tiny blood vessel hemorrhages)

Investigations:

  • Bloods: A full blood count (FBC) will show a decreased platelet count, while the clotting screen should be normal.
  • Blood Film: Giant platelets may be observed.
  • Bone Marrow Biopsy: The number of megakaryocytes may be normal or increased.

Treatment:

  • Medical: If platelet count is <30 x109/L, steroids or immunosuppression therapy should be considered.
  • Surgical: Splenectomy is also an option.

Complications:

Life-threatening bleeding may occur, and risk of life-threatening infections may arise following splenectomy or immunosuppression.

Prognosis:

The prognosis for this condition is good if treated early.

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