Low platelets (thrombocytopenia) may reflect reduced marrow production, increased destruction or consumption, splenic sequestration, or dilution. If the result is unexpected or isolated, first consider pseudothrombocytopenia from platelet clumping and confirm with a repeat count or smear.
Common settings include marrow suppression or infiltration (B12/folate deficiency, alcohol, chemotherapy, aplastic or malignant marrow disease), immune or drug-induced thrombocytopenia, infection/sepsis, consumptive microangiopathic processes (DIC, TTP/HUS, HELLP), hypersplenism, and chronic liver disease or portal hypertension.
High platelets (thrombocytosis) are most often reactive / secondary, especially with iron deficiency, inflammation, infection, recent bleeding or surgery, tissue injury, malignancy, or hyposplenism/splenectomy. In these cases, the platelet count often improves when the trigger resolves.
Persistent, unexplained, or marked thrombocytosis raises concern for a clonal myeloid disorder, especially essential thrombocythemia, polycythemia vera, primary myelofibrosis, or CML.


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