Anemias Flashcards
Spherocytosis
Defect in ankyrin
Hyperchromic, extravascular, hemolysis
Elliptocytosis
Defect in spectrin
Protective against malaria
PK deficiency
Decreased ATP, increased 2,3BPG, rigid RBC
Normocytic normochromic
G6PD deficiency
Decreased NADPH, decreased GSSG and increased ROS - damage
Heinz bodies, episodic
PNH
Defect in PIGA/GPI anchor/CD55&59
March hemoglobinuria/foot strike
Trauma from running, small blood vessels
WAIHA
IgG ran with Rh at 37 degrees
Extravascular
IgG+
Decreases platelet, microspherocytes
CAD
Type of CAIHA
Can be extravascular or intravascular
C3 and IgM positive
DAT/Coombs test
Anti IgG and anti C3 - immune mediated
PCH
Kids with respirator infection, dark urine
Intravascular
C3+
Biphasic IgG activates complement in cold and dissociates in warm so only C3 positive
Drug induced
Antibiotics - IgG - extravascular
Quinidine - C3+ - intravascular
Iron deficiency anemia
Microcytic, normochromic
Decreased Fe, serum ferritin (less storage), % transferrin (not much iron to bind)
Increased TIBC (body trying to scavenge more)
Low hepcidin
Hepcidin
Inhibits iron absorption
Hi - no iron absorbed
Lo - iron absorbed
Thalessemia
Microcytic, hypochromic
Decreased RBC, Hb, erythropoiesis
Decreased ferritin
Sideroblastic anemia
Hereditary
No heme, but excess free iron, ring sideroblasts
Increased iron, decreased TIBC, increased % transferrin, increased ferritin
Anemia of chronic disease
Mild hypochromic, microcytic
Decreased Fe, TIBC, % transferrin, increased ferritin
Presence of IL-1 & TNF can decrease EPO
Megaloblastic anemia
Macrocytic anemia
Larger, oval, hyperhsegmented nucleus
Decreased reticulocytes
Can be caused by B12 or B9 deficiency
B12 deficiency
B12 from diet absorbed in ileum
Build up of MMA and homocysteine
Pernicious anemia
Autoimmune attack of IF, decreased B12
B9 deficiency
B9 absorbed in SI
Needed for purine and pyrimidines
Build out of homocysteine
Sickle cell anemia
Normocytic, bite cells
Vasoocclusion pain crisis, ischemia, acute chest syndrome, splenic sequestration
Treat with hydroxyurea (increases HbF)
Alpha thalassemia
Silent, trait/mild, disease , hydrous fetalis
Causes HbH = B tetramers
Some HbBarts = Y tetramers - hemolytic
Beta thalassemia
Carrier - intermediare - major = Cooley’s, transfusion dependent
Symptomatic at 3 months when HbF drops
Increased EPO - bone deformation