PLATELETS

platelet lineage

• Platelets

thrombocytopenia


• Thrombocytopenia (low platelet count) results from 3 main mechanisms: decreased production, increased consumption/destruction, and abnormal distribution:
   Decreased production: due to marrow dysfunction due to primary (e.g. Fanconi anemia) or acquired (e.g. marrow infiltration) causes or ineffective thrombopoeisis (e.g. nutritional deficiency)
   Increased consumption or destruction: mediated by enhanced immune response (e.g. ITP, TTP), infection, drug, or shear stress
   Abnormal distribution: due to splenic sequestration in hypersplenism or hemodilution


THROMBOCYTOPENIA

✿ Pseudothrombocytopenia
  ✧ artifact (edta)
  ✧ antibodies (IgG, IgM, IgA)
  ✧ glycoprotein iib/iiia inhibitors

✿ Decreased production
  ✧ Fanconi anemia
  ✧ acquired aplastic anemia
  ✧ myelodysplasia
  ✧ myelofibrosis
  ✧ neoplastic infiltration
    ☼ leukemia
    ☼ lymphoma
    ☼ metastatic cancer
  ✧ paroxysmal nocturnal hemoglobinuria
  ✧ hemophagocytic lymphohistiocytosis
  ✧ vitamin b12/ folate deficiency
  ✧ chronic alcohol abuse
  ✧ thyroid disorders
  ✧ infection
    ☼ parvovirus, hiv, hcv, ebv, cmv
    ☼ tuberculosis, brucellosis
  ✧ immunosuppressants


✿ Increased destruction
  ✧ immune thrombocytopenic purpura
  ✧ thrombotic thrombocytopenic purpura
  ✧ hemolytic uremic syndrome
  ✧ disseminated intravascular coagulopathy
  ✧ pregnancy (hellp)
  ✧ infection
    ☼ virus (hiv, hcv, ebv)
    ☼ protozoa (malaria, babesia)
    ☼ bacteria (h pylori)
  ✧ drugs
    ☼ heparin (hit)
    ☼ quinidine
    ☼ abciximab
  ✧ posttransfusion purpura
  ✧ shear stress
    ☼ hemodialysis
    ☼ cardiopulmonary bypass
    ☼ ecmo

✿ Abnormal distribution
  ✧ hypersplenism (splenomegaly)
  ✧ hemodilution

thrombocytosis


• Thrombocytosis (high platelet count) results from either:
   Primary disorders: such as essential thrombocythemia or polycythemia vera
   Secondary disorders: such as reactive thrombocytosis (e.g. in response to anemia, thrombocytopenia, inflammation) or induced production by drugs (e.g. growth factors)
   Abnormal distribution: or relative thrombocytosis seen in asplenia or hemoconcentration


THROMBOCYTOSIS

✿ Abnormal distribution (relative)
  ✧ asplenia
  ✧ hemoconcentration

✿ Primary causes
  ✧ essential thrombocythemia
  ✧ polycythemia verA


✿ Secondary causes
  ✧ anemia
    ☼ acute blood loss
    ☼ iron deficiency anemia
    ☼ hemolytic anemia
  ✧ rebound from thrombocytopenia s/p treatment
  ✧ inflammation
    ☼ infection (acute & chronic)
    ☼ autoimmune disorders (ibd, ra)
    ☼ tissue injury/ trauma
    ☼ malignancy
  ✧ drugs
    ☼ growth factors (thrombopoietin)
    ☼ vincristine
    ☼ epinephrine
    ☼ steroids
    ☼ all-trans retinoic acid

platelet dysfunction


• Platelet dysfunction (qualitative)


PLATELET DYSFUNCTION

✿ Inherited disorders
  ✧ bernard-soulier syndrome
  ✧ glanzmann thrombasthenia
  ✧ von willerbrand disease
  ✧ storage pool disease
    ☼ gray platelet syndrome
    ☼ chediak-higashi syndrome
  ✧ wiskott-aldrich syndrome
  ✧ scott syndrome
  ✧ platelet release disorders
  ✧ sitcky platelet syndrome


✿ Acquired disorders
  ✧ uremia
  ✧ liver disease
  ✧ disseminated intravascular coagulopathy
  ✧ cariopulmonary bypass
  ✧ myeloproliferative disorders
  ✧ paraproteinemia
    ☼ multiple myeloma
    ☼ macroglobulinemia
  ✧ acquired von willerbrand syndrome
  ✧ infection (hiv)
  ✧ drugs
    ☼ nsaids
    ☼ antiplatelets
    ☼ anticoagulants
    ☼ thrombolytics
    ☼ antibiotics
    ☼ cardiovascular drugs
    ☼ chemotherapy

platelet morphology


• Platelets are small, anuclear cells derived from megakaryocytes down the myeloid lineage (illustrated above).
• The presence of large platelets (megathrombocytes) might suggest abnormal (e.g. giant platelet disorders) or increased megakaryocyte/ platelet production due to increased destruction (e.g. microangiopathy, ITP) or uncontrolled proliferation (e.g. myeloproliferation).

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peripheral blood smear platelets morphology

related topics




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