CH 13 BLOOD PATHOLOGY Flashcards
anemia
deficiency in erythrocytes or hemoglobin; caused by a lack of iron which is needed for hemoglobin production
aplastic anemia
failure of blood cell production in the bone marrow. usually idiopathic but few cases have been linked to benzene.
pancytopenia
occurs when stem cells fail to produce leukocytes, platelets and erythrocytes. antibiotics control infections and blood transfusion can prolong life. also bone marrow transplantation and immunosuppressive therapy.
hemolytic anemia
reduction of red blood cells due to excessive destruction.
congenital spherocytic anemia
hereditary spherocytosis- instead of the biconcave shape, erythrocytes are spheroidal. makes them fragile resulting in hemolysis. removal of spleen can help since the spleen helps destroy red blood cells.
sickle cell anemia
hereditary disorder of abnormal hemoglobin producing sickle-shaped erythrocytes and hemolysis. sickle-shaped red blood cells. a genetic defect hat is inherited. gene therapy possible. these patients are immune to malaria because the parasite cannot infect their cells.
thalassemia
inherited disorder of abnormal hemoglobin production leading to hypochromia. a gene defect affects production of globin, the protein that makes hemoglobin. so there is diminished hemoglobin content in red blood cells.
thalassa
means sea
pernicious anemia
lack of mature erythrocytes caused by inability to absorb vitamin b12 into the bloodstream. b12 necessary for erythrocytes. b12 cannot be absorbed without intrinsic factor which people with this lack. treatment is b12 injections for life. used to be fatal within 6 months before it was figured out.
hemochromatosis
excess iron deposits throughout the body. can be hereditary or caused by frequent blood transfusions.
polycythemia vera
general increase in red blood cells (erythremia). blood is viscuous because of a great number of erythrocytes. the bone marrow is hyperplastic, and leukocytosis and thrombocytosis are common. treatment is having blood removed and suppressing blood cell production with myelotoxic drugs.
hemophilia
excessive bleeding caused by hereditary lack of factors VIII or IX necessary for blood clotting. blood does not clot easily. progress is being made with gene therapy. typically affects majority males because these factors are located on the X gene, of which males only have one.
purpura
multiple point hemorrhages and accumulation of blood under the skin. reddish or bluish skin discoloration. petechia and ecchymoses are present. its a deficiency of platelets ( “autoimmune” thrombocytopenic purpura). immunologic, meaning the body produces antiplatelet factors that harm the platelets. splenectomy can treat it and immunosuppressive therapy.
leukemia
increase in malignant white blood cells.
acute myeloid leukemia
AML- immature granulocytes predominate. platelets and erythrocytes are diminished because of overproduction of myeloblasts. affects mainly adults and treated with chemo but remission is common. stem cell therapy may cure.
acute lymphoid (lymphocytic) leukemia (ALL)
immature lymphocytes (lymphoblasts) predominate. mostly in children, treated with chemo.
chronic myeloid (myelocytic) leukemia (CML)
mature and immature granulocytes are present. slowly progresses. both adults and children. drug therapy may control.
chronic lymphoid (lymphocytic) leukemia (CLL)
abnormal numbers of mature lymphocytes everywhere. usually in elderly and slowly progresses. does not require immediate treatment.
remission
disappearance of signs and symptoms of disease
relapse
symptoms and signs of disease reappear