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Bleeding disorders are a broad group of diseases that can be categorized under multiple different causes and clinical presentations. There are several different types of bleeding disorders that have several different etiologies. Most bleeding disorders are caused by defects in the body's normal blood clotting capability. Common causes of bleeding disorders are due to problems with normal functioning of platelets, clotting factors, blood vessels, and tissue integrity. Disorders involving certain aspects of the normal clot formation process can be due to an inherent disease process or genetic defect, they can be caused by adverse effects of certain medications, or they can be caused secondarily to other disease states. All these disorders share in common that an individual with this bleeding disorder will have an increased propensity to bleed as well as the inability to stop the bleeding and maintain normal homeostasis functioning.

Homeostasis is the body's capacity to maintain normal blood flow to essential organs and body parts through a series of blood vessels (i.e., arteries, capillaries, and veins) and supporting tissues. Homeostasis functions to maintain sufficient tissue perfusion by preventing excess formations of thromboses (clots inside blood vessels) as well as breaking up existing clots when required (disorders of this aspect of homeostasis are not going to be addressed in this entry, see Hypercoagulable Disorders). The body's homeostasis must also function to prevent the loss of blood by the ability to form clots when necessary. Defects in this component of homeostasis are the source of most bleeding disorders and will be addressed in this entry.

In cases of tissue damage in humans, the normal response of the body is to form clots to stop bleeding and initiate tissue repair. Blood clots are formed by the interaction of certain components of tissues, platelets, blood clotting factors and other blood signaling molecules. These compounds undergo various complex chemical interactions, thereby allowing the body to precisely regulate the extent of clotting at the exact site of injury. It is likely there will be some form of a bleeding disorder if the body has a defect in the functioning of the normal clotting system.

Platelet Disorders

One of the most common defects in clot formation is disorders of platelets. Defects can be due to decreased formation of platelets, increased destruction or consumption of platelets, or impairment in normal function of platelets. There are normally 150,000 to 450,000 platelets per cubic millimeter of blood and are made from cells called megakaryocytes in the bone marrow; decrease in number of platelets is called thrombocytopenia. Clinical features of thrombocytopenia are increase amount of bleeding, easy bruising, formation of petechia and purpura (skin rashes), prolonged bleeding time (time before bleeding stops after injury), and possible (potentially life-threatening) intracranial or gastrointestinal bleeding.

Thrombocytopenia is usually due to the decreased formation or increase destruction of platelets. Decreased formation of platelets can be due to (but not limited to) vitamin B12/folate deficiency, severe blood infections (sepsis), and certain leukemias. These diseases cause decrease in number or decrease in functioning of normal megakaryocytes in bone marrow, leading to decreased platelets. B12 and folate are required for normal proliferation of megakaryocytes and other blood cells in bone marrow, deficiency in these essential vitamins lead to thrombocytopenia and anemia. Severe infections of the blood cause inflammation, which decreases proliferation of megakaryocytes and decreases number of platelets. Leukemias, especially, can lead to severe platelet deficiency due to overgrowth of cells other than megakaryocytes within the bone marrow. One severe side effect in patients with leukemia is their increased propensity to bleed due to lack of platelets in the blood.

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