HEMOLYTIC ANEMIA

39 cards   |   Total Attempts: 188
  

Cards In This Set

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Characterized by what two things?
Decreased hg and decreased retic count
What can mimic this? but?
Acute blood loss (but an obvious site of bleeding would be identified usually)
Two main causes?
Extraerythrocytic factors (usually acquired) or intrinsic defects in the RBC (often inherited)
Where can hemolysis occur?
Intravascular space or in the extravasclar space (mainly spleen or liver)
Intravasc hemolysis--> rlease of hg, which gets bound to ____. the complex is ___ by the ___ system and the haptoglbin levels rapidly ___ to ___ or ____ levels
Haptoglobin; cleared; reticuloendothelial; low; undetectable
What happens once intravascular hg overload the haptoglobulin capacity?
Hg is filtered and reabsorbed by the kidney...tubular cells are sloughed off into the urine and are detected as urine hemosiderin...and when resorpstion is overwhelmed, hemoglobinuria can be detected (+ on urine dipstick)
In extravascular hemolysis, RBCs are ___ by ___ and ____ system---> ___ hg is released into the bloodstream. Haptoglobin may be ___, but urine hemosiderin and hemoglobinuria are usually ___ ___
Removed; spleen; RE; little; low; not present
2 major categories are extraerthrocytic factors and red blood cell defects. categories for each?
EF: microangiopathic hemolytic anemia (MAHA), immune-mediate hemolytic anemia, infections, splenomegaly.....RBCD: hemoglobinopathies (extra), enzyme defects (intravasccular), membrane defects
Types of MAHA? (4)
DIC, hemolytic uremic syndrome, thromobtic thrombocytopenic purpura, cardiac valve hemolysis
2 types of immune-mediated?
Warm antibody (hematolgoic malig, ct diosrders, drugs...extravascular); cold antibody (lymphoma, mycoplasma, mononucleosis...intravascular)
3 types of infections?
Malaria, babesiosis, clostridial toxin
2 causes of splenomegaly?
Infiltrative diseases, portal htn
Hemoglobinopathy? (extravascular)
Sickle cell disease
2 enzyme defects (intra)
Pyruvate kinase def, G6PD def
2 membrane defects?
Hereditary spherocytosis and elliptocytosis (extravascular), paroxysmal nocturnal hemoglobinuria (intravasc)