Platelet Size

Individuals with inherited platelet disorders experience lifelong abnormal bleeding, usually at mucocutaneous sites or elsewhere after trauma or invasive procedures. Inherited platelet disorders should be suspected in patients with lifelong thrombocytopenia; bleeding not explained by a coagulation factor deficiency; presentation with an associated condition; and patients with affected family members. Inherited platelet disorders can be caused by defects in surface membrane receptors, signaling pathways, granule formation and secretion, cytoskeletal remodeling and expression of procoagulant activity.

Laboratory testing for suspected inherited platelet disorders should begin with a complete blood count (CBC) and examination of a peripheral blood smear. CBC includes platelet count and mean platelet volume (MPV). An abnormal platelet count and MPV should be confirmed by examination of a peripheral blood smear. The following table contains a summary of platelet count and platelet size in various platelet disorders.

 

Platelet Disorder Platelet Count Reduction Platelet Size
Bernard Soulier Moderate to severe Giant
Familial platelet disorder associated with AML Mild to moderate Normal
GATA1-related thrombocytopenia Severe Large
Gray platelet syndrome Mild Large
Medich platelet syndrome Mild Large
MYH9 mutation associated disorders Mild to moderate Large
Paris-Trousseau syndrome Moderate to severe Normal to slightly increased
Platelet type vWD Mild Normal or slightly increased
Stormorken syndrome Mild to moderate Normal
Velocardiofacial syndrome Mild Large
Wiskott-Aldrich Severe Small
White platelet syndrome Mild Large

 

Reference range for MPV is 7.4-11.5 fL. MPV <6 fL is seen in Wiskott Aldrich syndrome and MPV >12 is seen in Bernard Soulier. If the platelet count and platelet size suggest that an inherited platelet disorder may be present, platelet function analysis (PFA-100) and platelet aggregation should be ordered. Abnormal findings in these tests may necessitate additional confirmatory tests including platelet electron microscopy, platelet flow cytometry and genotyping.

Updated Articles

Heparin Induced…

Heparin induced thrombocytopenia (HIT) is an antibody mediated adverse effect of heparin that is strongly associated with venous and arterial thrombosis. Major risk factors include exposure to unfractionated high molecular weight heparin for more…

New Articles

Myelin…

Myelin oligodendrocyte glycoprotein is a CNS antigen expressed on the myelin sheath. Approximately 5% of patients with neuromyelitis optica spectrum disorder (NMOSD) test negative for anti-neuromyelitis optica antibody (anti-AQP4) but have…

Blog

Oligoclonal Pattern…

Serum protein electrophoresis (SPEP) and serum immunofixation electrophoresis (SIFE) are important diagnostic tests for multiple myeloma. In approximately 80% of myeloma cases, a single monoclonal protein is detected. Detection of biclonal and…