Platelets are components of blood that aid in the formation of blood clots. Thrombocytosis arises when the body produces an excessive number of platelets. When this excess is triggered by an underlying condition, such as an infection, it is termed reactive or secondary thrombocytosis.
In rare cases where no apparent cause is identified, it is labeled primary thrombocythemia or essential thrombocythemia, a condition affecting both blood and bone marrow. The detection of elevated platelet levels often involves a routine blood test known as a complete blood count. It is essential to differentiate between reactive thrombocytosis or essential thrombocythemia to determine the appropriate course of treatment.
Individuals with elevated platelet counts may exhibit no symptoms at all. When symptoms appear, blood clots are frequently the cause. As examples, consider:
Extremely elevated platelet levels can lead to bleeding, resulting in:
Within your bones resides a spongy tissue known as bone marrow, containing stem cells capable of developing into platelets, white blood cells, or red blood cells. Platelets adhere to each other, aiding in the formation of a clot that halts bleeding when a blood vessel is injured, such as during a cut. However, an overproduction of platelets can result in thrombocytosis.
This kind of thrombocytosis is more typical. It is brought on by an underlying medical issue, like:
The exact cause of this condition remains unclear, but it often appears to be associated with changes in specific genes. In thrombocytosis, the bone marrow produces an excessive amount of cells responsible for platelets formation, often resulting in dysfunctional platelets. Unlike reactive thrombocytosis, this form carries a higher risk of clotting or bleeding complications.