Chapter 13: Blood System: Pathology and Laboratory Tests Flashcards
anemia
Deficiency in erythrocytes or hemoglobin
aplastic anemia
Failure of blood cell production in the bone marrow
pancytopenia
Occurs when stem cells fail to produce leukocytes, platelets, and erythrocytes
hemolytic anemia
Reduction in red cells due to excessive destruction
congenital spherocytic anemia
hereditary spherocytosis
Erythrocytes become spheroidal instead of their normal biconcave shape
pernicious anemia
Lack of mature erythrocytes caused by inability to absorb vitamin B12 into the bloodstream
sickle cell anemia
Hereditary disorder of abnormal hemoglobin producing sickle-shaped erythrocytes and hemolysis
thalassemia
Inherited disorder of abnormal hemoglobin production leading to hypochromia
hemochromatosis
Excessive iron deposits throughout the body
polycythemia vera
General increase in red blood cells (erythremia)
hemophilia
Excessive bleeding caused by hereditary lack of factors VIII and IX necessary for blood clotting
purpura
Multiple pinpoint hemorrhages and accumulation of blood under the skin
petechia
Tiny purple or red flat spots appearing on the skin as a result of hemorrhages
ecchymoses
Larger blue or purplish patches on the skin (bruises)
autoimmune thrombocytopenia purpura
Condition in which the patient makes an antibody that destroys platelets
leukemia
Increase in cancerous white blood cells (leukocytes)
acute myeloid (myelocytic) leukemia
Immature granulocytes (myeloblasts) predominate. Platelets and erythrocytes are diminished because of infiltration and replacement of the bone marrow by larger numbers of myeloblasts
acute lymphoid leukemia
Immature lymphocytes (lymphoblasts) predominate. This form is seen most often in children and adolescents; onset is sudden
chronic myeloid (myelocytic) leukemia
Both mature and immature granulocytes are present in large numbers in the marrow and blood