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AP MOD. I-Blood
| Term | Definition |
|---|---|
| Type O blood | universal donor blood |
| Type AB blood | universal recipient blood |
| polycythemia | overproduction of RBCs |
| anemia | low oxygen-carrying capacity of blood |
| hemorrghagic anemia | anemia caused by blood loss from trauma, ulcers, or cancer |
| aplastic anemia | anemia characterized by destruction of bone marrow |
| pernicious anemia | anemia caused by vitamin B12 deficiency |
| folate deficiency anemia | common in alcoholism and malnutrition |
| iron deficiency anemia | caused by inability to absorb iron |
| sickle cell anemia | genetic disease, RBCs are sickle shaped |
| thalassemia | RBCs are short lived, causes skeletal deformities and swelling of liver and spleen |
| erythroblastosis fetalis | hemolytic disease of newborn caused by ABO or Rh factor incompatibility between fetus and mother |
| RhoGAM | given during pregnancy to prevent Rh factor incompatibility |
| multiple myeloma | cancer of B lymphocytes, causes destruction and fracture of bones |
| leukemias | WBC-related blood cancers |
| chronic lymphocytic leukemia | (CLL)-generally mild symtoms occuring at age 65 |
| acute lymphocytic leukemia | (ALL)-sudden onset, primarily in children |
| chronic myeloid leukemia | (CML)-slow onset, most often in adults |
| acute myeloid leukemia | (AML)-sudden onset, rapid progression-most common |
| mononucleosis | noncancerous WBC disorder caused by a virus |
| thrombus | stationary blood clot |
| embolus | circulating blood clot |
| hemophilia | X-linked inherited bleeding disorder |
| thrombocytopenia | bleeding disorder characterized by purple spots in the skin |
| vitamin K deficiency | can result in abnormally reduced clotting |