Table 2.
| Primary or clonal | Secondary or reactive | Artefactual or spurious |
|---|---|---|
| Essential thrombocytosis | Acute blood loss | Erythrocyte fragments |
| Polycythaemia vera | Trauma | Schistocytes |
| Primary myelofibrosis | Surgery | Microcytosis |
| Familial/hereditary thrombocytosis | Infectious diseases | Spherocytosis |
| Chromosome 5q-deletion syndrome | Iron deficiency | Cryoglobulinaemia |
| Chronic myeloid leukaemia | Asplenia | Neoplastic fragments |
| Chronic myelomonocytic leukaemia | Malignancy | Bacteria |
| Atypical chronic myeloid leukaemia | Chronic inflammationa | Fungi |
| Myelodysplastic syndrome | Haemolysis | Lipid dropletsc |
| Unclassifiable myeloproliferative neoplasms | Allergic reactions | – |
| RARS‑T | Exercise | – |
| POEMS syndrome | Medicationb | – |
RARS‑T refractory anaemia with ringed sideroblasts associated with marked thrombocytosis.
POEMS acronym for a rare blood disorder with the following signs/symptoms: polyneuropathy, organomegaly, endocrinopathy/oedema, monoclonal protein, skin changes
aFor example, rheumatic diseases
bFor example, low-molecular-weight heparin, ceftazidime, clozapine, gemcitabine, non-steroidal anti-inflammatory drugs and steroids
cNotably when samples are taken shortly after a meal