Hematologic diseases Flashcards
iron deficiency anemia
poor absorption or excessive loss of iron
pernicious anemia
poor absorption of B12 due to absence of intrinsic factor
leads to low H&H, GI problems, neuro symptoms
Aplastic anemia
bone marrow without erythroid, myeloid, megakariocytic cell lines
Requires transfusions until bone marrow again produces cells
S/S: weakness, dyspnea, headaches
hemolytic anemia
RBC are destroyed, bone marrow cannot keep up with RBC loss
Thalassemia
genetic disorder leading to inadequate hemoglobin production
Polycythemia Vera
Over production of RBC, WBC, and platelets
Thick blood, large blood volume, organ congestion
S/S: Red complexion, dizziness, headache, visual disturbances, painful joints
Treatment: myelosuppresive drugs, radiation
Immune thrombocytopenia purpura
abnormal destruction and reduced production of circulating platelets, primarily an autoimmune disease
Hemophilia
X-linked recessive genetic disorder caused by a defective of deficient coagulation factor
Disseminated intravascular coagulation
widespread clotting
Causes: shock, sepsis, cirrhosis, severe trauma
usually a secondary event from activation of one of the coagulation pathways
Acute Leukemia
clonal proliferation of immature hematopoietic cells
Chronic Leukemia
Mature forms of WBC and onset is more gradual
Leukemia-ALL
childhood 80% of time, diagnosis by lymphoblasts in bone marrow, bleeding, anemia symptoms, joint pain
Leukemia- AML
advanced aging- 60 years, auer rod structure in cytoplasm of myeloblasts confirms diagnosis
Leukemia- CLL
age 55 or older, frequently detected incidentally, diagnosis by lymphocytosis, lymphadenopathy present 80%
Leukemia- CML
middle age 55 years, Philadelphia chromosome confirms diagnosis, main symptoms of fatigue and spleenomegaly