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Updated: Dec 4 2016

Glanzmann Thrombasthenia

Snapshot
  • A 2-month-old female baby is seen in the emergency room with frequent nosebleeds and bruising. Her birth history is unremarkable, except for delayed separation of the umbilical cord. On physical exam, there is some blood in his blood. Lab results show normal PT and PTT but increased bleeding time. Her platelets come back at a normal range. Peripheral blood smear shows no clumping of platelets.
Introduction
  • Impaired platelet aggregation from genetic deficiency of GpIIb/IIIa
  • Genetics
    • autosomal recessive
  • Pathogenesis
    • ↓ GpIIb/IIIa (a platelet integrin)
      • recall that GpIIb/IIIa is a receptor on platelets
      • fibrinogen interacts with GpIIb/IIIa between two platelets, helping platelet aggregation
      • recall abciximab inhibits this receptor
    • defect in platelet plug formation
  • Key lab finding
    • normal platelet count
    • ↑ bleeding time
  • Associated conditions
    • leukocyte adhesion deficiency commonly seen
      • impaired wound healing
      • delayed umbilical cord separation > 30 days
      • recurrent skin and mucosal infections
    • acquired Glanzmann thrombasthenia
      • in those who received multiple platelet transfusions
Presentation
  • Symptoms from platelet abnormalities
    • mucocutaneous microhemorrhages
      • bleeding from mucous membranes
      • epistaxis
      • petechiae/purpura
Evaluation
  • ↑ bleeding time
  • Normal PT/PTT
  • Complete blood count
    • normal platelet count
    • normal platelet morphology
  • Peripheral blood smear
    • no platelet clumping seen
Differential Diagnosis
  • Bernard-Soulier (↓ platelet count, ↑ bleeding time, and ↓ GpIb)
  • ITP (↓ platelet count, ↑ bleeding time, and anti-GpIIb/IIIa antibodies)
  • TTP (↓ platelet count, ↑ bleeding time, and defective/deficient ADAMTS13)
Treatment
  • Platelet transfusions
    • with HLA-matched and leukocyte depleted blood products
  • No clear evidence but options are
    • recombinant factor VIIa
    • hematopoietic stem cell transplant
  • Supportive care
    • iron and folate supplementation
Prognosis, Prevention, and Complications
  • Prognosis
    • good with supportive care
    • generally, bleeding decreases with age
  • Prevention
    • avoid anti-platlet agents (aspirin and NSAIDs)
  • Complications
    • uncontrolled bleeding
Private Note

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