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eim chap 13
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131 Terms
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monocyte
mononuclear white blood cell formed in lymph tissue; it is a phagocyte and the precursor of a macrophage
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platelet
thrombocyte or cell fragment that helps blood clot
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hematopoietic stem cell
cell in the bone marrow that gives rise to different types of blood cells
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lymphocyte
mononuclear leukocyte formed in lymph tissue; produces antibodies
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eosinophil
leukocyte with dense, reddish granules having an affinity for red acidic dye; associated with allergic reactions
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erythrocyte
red blood cell
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neutrophil
leukocyte (polymorphonuclear granulocyte) formed in the bone marrow; granules do not stain intensely and have a pale color
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basophil
leukocyte (granulocyte) with dark-staining blue granules; releases histamine and heparin
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coagulation
blood clotting
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granulocyte
white blood cell with numerous, cytoplasmic granules (neutrophil, basophil, and eosinophil)
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mononuclear
pertaining to a leukocyte with a single round nucleus; monocytes and lymphocytes are mononuclear leukocytes
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polymorphonuclear
pertaining to a white blood cell with a multilobed nucleus; neutrophil
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globulin
plasma protein; alpha, beta, and gamma (immune) globulins are examples
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erythroblast
immature red blood cell
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megakaryocyte
large platelet precursor (forerunner) cell found in bone marrow
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macrophage
monocyte that migrates from blood to tissue spaces; phagocyte that engulfs foreign material and ingests red blood cells
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hemoglobin
blood protein containing iron; carries oxygen in erythrocytes
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plasma
liquid portion of blood
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myeloblast
immature bone marrow cell that gives rise to granulocytes
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bilirubin
orange-yellow pigment produced from hemoglobin when red blood cells are destroyed
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fibrinogen
plasma protein converted to fibrin in clotting process
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erythropoietin
hormone secreted by the kidneys to stimulate bone marrow to produce red blood cells
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antigen
hormone secreted by the kidneys to stimulate bone marrow to produce red blood cells
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albumin
protein in blood that maintains the proper amount of water in the blood
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antibody
specific protein produced by lymphocytes in response to antigens in the blood
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heparin
anticoagulant found in blood and tissue cells
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serum
plasma minus clotting proteins and cells
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differentiation
change in structure and function of a cell as it matures
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colony-stimulating factor
protein that stimulates growth of developing blood cells
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4 types of plasma proteins
albumin
globulins
fibrinogen
prothrombin
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Rh factor
an antigen normally found on red blood cells
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hemolysis
destruction or breakdown of red blood cells
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A person with type A blood has
A antigens and anti-B antibodies in blood
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A person with type B blood has
B antigens and ani-A antibodies in blood
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A person with type O blood has
NO A or B antigens but has anti-A and anti-B antibodies in blood
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A person with type AB blood has
A and B antigens but has NO anti-A and anti-B in blood
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Can you transfuse blood from a type A donor into a type B recipient? Why or Why not?
No. A antigens will react with the anti-A antibodies in the type B recipient's bloodstream
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Can you transfuse blood from a type AB donor into a type O recipient? Why or why not?
No. A and B antigens will react with the anti-A and anti-B antibodies in the type O recipient's bloodstream
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immunoglobulin
protein with antibody activity; IgG, IgH, IgE
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plasmapheresis
removal by centrifuge of plasma from withdrawn blood
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Why is a person with type O blood the universal donor?
type O blood does not contain A or B antigens and therefore will not react with antibodies in any recipient's blood
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anticoagulant substance found in liver cells, blood, and tissues
heparin
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protein thread that forms the basis of a blood clot
fibrin
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plasma protein that is converted to thrombin in the clotting process
prothrombin
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plasma minus clotting proteins and cells
serum
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drug given to patients to prevent formation of clots
warfarin (coumadin)
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plasma protein that is converted to fibrin in the clotting process
fibrinogen
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process of clotting
coagulation
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enzyme that helps convert fibrinogen to fibrin
thrombin
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anticoagulant
a substance that prevents clotting
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hemoglobinopathy
disease (abnormality) of hemoglobin
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cytology
study of cells
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leukopenia
deficiency of white blood cells
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morphology
study of the shape or form (of cells)
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cell with a large (mega-) nucleus (kary); platelet precursor
megakaryocyte
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sideropenia
deficiency of iron
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cell that eats or swallows other cells
phagocyte
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formation of the bone marrow
myelopoiesis
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separation of platelets from the rest of the blood
plateletpheresis
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monoblast
immature monocyte
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abnormal (ineffective) production of myeloid cells in bone marrow
myelodysplasia
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myeloid progenitor cells
give rise to erythrocytes, granulocytes, and platelets
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hemostasis
controlling or stopping the flow of blood
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thrombolytic (therapy)
pertaining to treatment using drugs to destroy clots
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hematopoiesis
formation of blood cells
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myeloid
derived in bone marrow
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neutropenia
deficiency of a type of neutrophils
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hematocrit
percentage of red blood cells in a volume of blood
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increase in a type of white blood cell (seen in allergies)
eosinophilia
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thrombosis
abnormal condition of clot formation
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leukapheresis
separation of white blood cells from a blood sample
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coagulopathy
disease of clotting process
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deficiency of platelets
thrombocytopenia
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poikilocytosis
any irregularity in the shape of red blood cells
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hemoglobin
oxygen-containing protein in red blood cells
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formation of red blood cells
erythropoiesis
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anemia
deficiency in numbers of red blood cells
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hypochromic
pertaining to reduction of hemoglobin in red blood cells
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anisocytosis
variation in size of red blood cells
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spherocytosis
abnormal numbers of round, rather than normally biconcave-shaped, red blood cells
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microcytosis
increase in number of small red blood cells
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polycythemia vera
general increase in numbers of red blood cells; erythremia
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macrocytosis
increase in numbers of large red blood cells
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separation of blood so that the percentage of red blood cells in relation to the volume of a blood sample is measured
hematocrit
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lack of iron leading to insufficient hemoglobin production
iron deficiency anemia
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lack of mature erythrocytes caused by inability to absorb vitamin B12 into the bloodstream
pernicious anemia
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intrinsic factor
missing in gastric juice, so B12 is not absorbed
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hereditary disorder of abnormal hemoglobin producing sickle-shaped erythrocytes and hemolysis
sickle cell anemia
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failure of blood cell production in bone marrow
aplastic anemia
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inherited disorder of abnormal hemoglobin production leading to hypochromia
thalassemia
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multiple pinpoint hemorrhages and accumulation of blood under the skin (cause may be deficiency of platelets)
purpura
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abnormal increase in granulocytes in the blood (eosinophilia and basophilia)
granulocytosis
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excessive bleeding caused by hereditary lack of blood clotting factors
hemophilia
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excessive iron deposits throughout the body
hemochromatosis
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malignant neoplasm of bone marrow
multiple myeloma
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infectious disease marked by increased numbers of mononuclear leukocytes and enlarged cervical lymph nodes
mononucleosis
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relapse
Symptoms of the disease return
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remission
Symptoms of the disease disappear
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palliative
Relieving but not curing
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Bence Jones protein
Immunoglobulin fragment found in the urine of patients with multiple myeloma
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