thrombocytopenia Flashcards

1
Q
  • Direct damage of endothelium due to toxin, infection or drug.
  • SHIGA toxin produced by toxigenic strain of E-COLI O157:H7
  • Toxin damages the endothelial cells within the glomeruli and promotes the adhesion of platelets and trapping of RBCs.
  • Medicines like calcinuerin inhibitors (tacrolimus, cyclosporine) and cytotoxic drugs ( mitomycin C , cisplatin & Bleomycin) can induce it by direct damage to endothelial cells.
A

HEMOLYTIC UREMIC SYNDROME -
HUS

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2
Q

hemolytic uremic syndrome treatment

A
  • Reducing the spread of Shiga-toxin
    producing E-coli is vital.
  • Plasma exchange is standard of care in adults.
  • Aggressive antibiotic therapy appears to be beneficial for reducing seizures and death
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3
Q
  • caused by circulating anti platelet antibodies
  • children: acute ITP and rarely have chronic variant
  • adults: chronic recurring disorder
  • viral illness like HIV or Hepatitis C may induce it
A

idiopathic (immune) thrombocytopenic purpura

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4
Q

wet bleeding
- excessive mucocutaneous bleeding
- epistaxis
- gingival bleeding

  • patechae
  • ecchymosis
  • retinal hemorrhage
  • no splenomegaly
  • normal CBC except thrombocytopenia
  • peripheral smear shows large platelets and no schistocytes
A

idiopathic (immune) thrombocytopenic purpura signs and symptoms

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5
Q

idiopathic (immune) thrombocytopenic purpura treatment

A
  • monitor platelet levels
  • glucocorticocoids (prednisone or dexamethasone)
  • IVIG
  • anti D immunoglobulins
  • splenectomy (relapse)
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6
Q
  • Decrease activity of protease ADAMTS-13
  • decrease cleavage of high molecular weight V-WBF polymer
  • abnormal activation of platelets
  • Fibrin deposition with vessel occlusion
  • Blood cells fragmentation
  • Microangiopathic hemolysis and
    thrombocytopenia.
A

THROMBOTIC THROMBOCYTOPENIC PURPURA- TTP

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7
Q

thrombotic thrombocytopenic purpura treatment

A
  • Plasma exchange ( apheresis in which native plasma is exchanged with FFP).
  • Plasma exchange remove antibody
    against ADAMTS-13 and replete
    deficiency of ADMATS-13
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