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82 Cards in this Set

  • Front
  • Back

blood

made up of cells and plasma


1. cells - 45%


2. plasma - 55%

cells

the portion of blood that consists of erythrocytes, leukocytes, and thrombocytes

plasma

the portion of blood made up of water, sugar, proteins, salts, hormones, lipids, and vitamins

A, B, AB, O

blood types

Type O

universal donor

Type AB

universal recipient

chrom/o

root for color

coagul/o

root for clotting

erythr/o

root for red

hem/o, hemat/o

roots for blood

is/o

root for same, equal

myel/o

root for bone marrow

poikil/o

root for varied, irregular (usually shape)

sider/o

root for iron

spher/o

root for round, globe

thromb/o

root for clot

-apheresis

suffix for removal, carrying away

-blast

suffix for immature cell

-cytosis

suffix for abnormal condition

-globin/-globulin

suffix for protein

-lytic

suffix for pertaining to the destruction of

-penia

suffix for deficiency

-philia

suffix for attraction for

-phoresis

suffix for carrying transmission

colony stimulating factor (CSF)

protein that stimulates the growth of WBCs

electrophoresis

method of separating serum proteins by electrical charge

plasmapheresis

removal of plasma from blood by centrifuge (the collected cells are transfused back into the donor)

red blood cells

1. erythroblast -> reticulocyte -> erythrocyte


2. Have a biconcanve shape with a central depression


3. Life span of 120 days

anemia

deficiency in erythrocytes/hemoglobin

aplastic anemia

an anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements

pancytopenia

lack of peripheral blood elements (not the anemia)

hemolytic anemia

general term covering a large group of anemias, in which there is a shortened life span of the RBCs (usually due to destruction)

hemolytic disease of the newborn

a hemolytic anemia that is usually caused by blood group incompatibility between the mother and the baby

hereditary spherocytosis and hereditary elliptocytosis

abnormal RBC membrane hemolytic anemias

sickle cell anemia and thalassemia

abnormal hemoglobin hemolytic anemia

hemoglobin

oxygen carrying molecule that fills the RBC

hereditary spherocytosis

an anemia that results in the formation of spherocytes

spherocytes

RBCs that are almost spherical in shape and have no area of central pallor like a normal RBC


sickle cell anemia

an inherited hemoglobinopathy that is characterized by the irreversibly crescent or sickle-shaped RBCs, increased hemolysis, painful crisis, and increased susceptibility to infections

thalassemia

a group of inherited disorders that affect the synthesis of hemoglobin, resulting in hypochromic and microcytic RBCs

beta-thalassemia

thalassemia caused by a deficient synthesis of beta globin. Requires transfusion therapy to sustain life

alpha-thalassemia

thalassemia caused by a deficient synthesis of alpha globin

pernicious anemia

a megaloblastic anemia caused by the lack of intrinsic factor (responsible for the absorption of B12) from the parietal cells in the gastric mucosa

B12

a vitamin necessary for the proper development and maturation of erythrocytes

folic acid deficiency anemia

a megaloblastic anemia produced by the deficiency of folic acid

folic acid

a nutrient that is essential for DNA synthesis and is mainly present in fruits and vegetables

iron deficiency anemia

a hypochromic and microcytic anemia that is caused by an underlying condition. The microcytic RBCs are all a different size (anisocytosis). It is the most common type of anemia world wide.

hemochromatosis

genetic condition causing excessive deposits of iron throughout the body, resulting in iron overload

polycythemia vera

the general increase in RBCs (generally also results in the increase of leukocytes and platelets)

erythremia

the term used to describe the general increase in RBCs

hemophilia

inherited bleeding disorder secondary to clotting factor deficiency

hemophilia A

hemophilia caused by the deficiency of factor VII

hemophilia B (Christmas disease)

hemophilia caused by the deficiency of factor IX

Von Willebrand's disease

hemophilia caused by the deficiency of Von Willibrand's factor

purpura

bleeding under the skin, resulting in multiple pinpoint hemorrages and the accumulation of blood under the skin (petechiae and ecchymosis)

petechiae

tiny, pinpoint flat spots of blood appearing on the skin

ecchymosis

a large bruise

ITP (idiopathic thrombocytopenia purpura)

a decrease in platelets after infection (<100,000) that can lead to brusiing, bleeding gums, GI bleeds, gyn bleeding, and a prolonged bleeding time

leukemia

a cancer involving WBCs, resulting in immature blood cells in the bone marrow and peripheral circulation, producing an array of neoplastic disorders

lymphocytic leukemia (ALL/CLL)

leukemia resulting in the predominance of lymphocytes

myelogenous leukemia (AML/CML)

leukemia resulting in the predominance of myeloid cells

chronic lymphocytic leukemia (CLL)

most common form of leukemia, often found in the elderly

acute lymphocytic leukemia (ALL)

the leukemia most often seen in children

granulocytosis

an abnormal increase in granulocytes in the blood

eosinophilia

a type of granulocytosis resulting in the increase of eosinophils. Seen with allergic conditions

basophilia

a type of granulocytosis resulting in the increase basophils. Seen with types of leukemia

mononucleosis

an acute, self-limited infection that occurs mainly in adolescents. Caused by the Epstein-Barr virus (EBV) and is transmitted mainly through saliva

multiple myeloma

the malignant tumor of the bone, resulting in a tumor of plasma cells

Bence Jones protein

Plasma proteins in the urine. A classic sign of multiple myeloma.

antiglobulin test (Coombs' test)

a test that detects antigen-antibody complexes on the RBC membrane in vivo as well as RBC sensitization

bleeding time

measures the primary phase of hemostasis (the interaction of the platelet with the blood vessel wall and the formation of a hemostatic pluc)

coagulation time

time required for venous blood to clot in a test tube

complete blood count (CBC)

a test that measures the contents of the blood

erythrocyte sedimentation rate

the rate at which erythrocytes settle out of the anticoagulated blood in 1 hour

sedimentation

occurs when the erythrocytes clump or aggregate together in a column-like manner (rouleaux formation)

hematocrit (Hct)

test that indirectly measures the RBC mass. The results are expressed as a percentage by volume of packed RBCs in the whole blood

hemoglobin

the main component of erythrocytes that serves as a vehicle for the transportation of oxygen and carbon dioxide

platelet count

measure the amount of platelets in the blood

platelets (thrombocytes)

the smallest of the formed elements in the blood

partial thromboplastin time (PTT)

a one-stage clotting test that screens for coagulation disorders. It can deficiencies of the intrinsic thromboplastin system and also reveals defects in the extrinsic coagulation mechanism pathway. Used to monitor heparin

prothrombin time (pro time/PT)

tests the ability of the blood to clot. Used to evaluate therapy with coumadin

prothrombin (factor II)

a protein produced by the liver for the clotting of blood. During the clotting process, it is converted to thrombin.