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Thrombotic Thrombocytopenic Purpura - StatPearls - NCBI Bookshelf
2023年4月7日 · Thrombotic thrombocytopenic purpura (TTP) is a microangiopathic hemolytic anemia classically characterized by the pentad of fever, hemolytic anemia, thrombocytopenia, and renal and neurologic dysfunction.
Thrombotic Thrombocytopenic Purpura - Cleveland Clinic
Thrombotic thrombocytopenic purpura (TTP) is a rare blood disorder in which thrombi (blood clots) form in small blood vessels throughout your body. These blood clots can restrict the flow of oxygen-rich blood to your organs, causing a number of life-limiting complications.
Thrombotic thrombocytopenic purpura - Wikipedia
Thrombotic thrombocytopenic purpura (TTP) is a blood disorder that results in blood clots forming in small blood vessels throughout the body. [2] This results in a low platelet count, low red blood cells due to their breakdown, and often kidney, heart, and brain dysfunction. [1]
Platelet Disorders Thrombotic Thrombocytopenic Purpura (TTP)
2022年3月24日 · “Thrombocytopenic” means the blood has a lower-than-normal platelet count. “Purpura” refers to purple bruises caused by bleeding under your skin. TTP usually occurs suddenly and lasts for days or weeks, but it can continue for months.
Thrombotic thrombocytopenic purpura - MedlinePlus
Thrombotic thrombocytopenic purpura is a rare disorder that causes blood clots (thrombi) to form in small blood vessels throughout the body. These clots can cause serious medical problems if they block vessels and restrict blood flow to organs such as the brain, kidneys, and heart.
Thrombotic Thrombocytopenic Purpura (TTP) - Blood Disorders ...
Thrombotic thrombocytopenic purpura (TTP) is a rare disorder in which many small blood clots (thrombi) form suddenly throughout the body. It is related to hemolytic-uremic syndrome (HUS), but it is more likely to occur in adults than HUS, which is more common in children.
Thrombotic Thrombocytopenic Purpura (TTP) - Hematology …
Thrombotic thrombocytopenic purpura (TTP) is an acute, fulminant disorder characterized by thrombocytopenia, microangiopathic hemolytic anemia, and sometimes organ damage. Clinical manifestations may include alterations in level of consciousness and kidney failure.