Just a quick remainder that Thrombotic thrombocytopenia Purpura, TTP, is typically described as a pentad of symptoms:
Neurological symptoms such as altered mental status, stroke, or headache
Renal failure
Fever
Thrombocytopenia (low platelets) associated with purpura
Microangiopathic hemolytic anemia
Not all symptoms need to be present and it would be rare for you to see the full pentad. Consider the diagnosis and request that the lab due a manual differentiation or blood smear. It is there that they will notice schistocytes, fragmented RBCs, that will help clinch the diagnosis.
Most cases of TTP are idiopathic (~60%) but secondary TTP is known to occur with cancer, pregnancy, HIV, bone marrow transplantation, immunospressive drugs like cyclosporin and tacrolimus, and platelet aggregation inhibitors such as cloperidol.
Treatment consists of plasmapheresis, plasma exchange, immunospression with steroids, Rituximab, and other chemotherapies.
