Thrombocytosis is a common finding and is a frequent cause of referral for further investigation. There is a wide range of primary (eg, essential thrombocythaemia (ET), other myeloproliferative neoplasm MPN) and secondary causes as well as false or ‘spurious’ conditions mimicking thrombocytosis. Much less commonly there is a primary cause (eg, ET, other MPN). Establishing the cause therefore requires consideration of clinical features, haematological parameters and other test results.
The most common secondary (or reactive) causes of thrombocytosis are infection, inflammation, iron deficiency, tissue damage, haemolysis, severe exercise, malignancy, hyposplenism and other causes of an acute phase response. These are usually, but not always, characterized by an elevated C-reactive protein.