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92 Cards in this Set

  • Front
  • Back
Kidney derived hormone that increases RBC production
erythropoietin (EPO)
Things that increase EPO production
hypoxemia, severe anemia, left shift in O2 binding curve, high altitude

basically anything that decreases oxygenation of your tissues
Things that decrease EPO production
anything that increases O2 content (such as polycythemia vera)
Abnormal things that make EPO
renal cell carcinoma
hepatocellular carcinoma
Where is EPO made?
endothelial cells of peritubular capillaries
Effective erythropoiesis is measured by
reticulocyte count
normal retic count percentage
< 3%
In anemia, retic count percentage is falsely...
elevated
Formula to correct retic count in anemia
Corrected retic = (actual Hct/45) x retic count
Anemic person with low retic count means
poor BM response (ineffective erythropoiesis)
Anemia + low retic count

Causes?
Fe def
aplastic
Extramedullary hematopoiesis occurs when?
intrinsic BM disease (myelofibrosis)
increased EPOesis (sickle cell, etc)
Extramedullary hematopoiesis can occur where?
spleen
liver
Findings on PE for EMH?
hepatosplenomegaly
Findings in radiograph for EMH?
expanded marrow cavity
hair on end appearance of skull
types of globin chains found in HbF
alpha (a)
gamma (y)
increased HbF causes what kind of O2 binding curve, which will cause what?
left shift

increased EPO
How does an infant get rid of HbF?
splenic macrophages


hence the physiologic jaundice
how does testosterone affect erythropoiesis?
increases EPOesis
MCV < 80

this is called
microcytic
MCV > 100
macrocytic
causes of microcytic anemias
Fe def
anemia of chronic disease
thalassemias
sideroblastic anemia
key lab finding with Fe def anemia
inc RDW
most common anemia
Fe def
causes of macrocytic anemia
folate def
B12 def
If normocytic anemia w/ corrected retic < 3%, name 5 causes
acute blood loss
early Fe def
early anemia of chronic disease
aplastic
renal disease
If normocytic anemia w/ corrected retic >/= 3%, it can be due to one of two general things...
intrinsic RBC defect or extrinsic RBC defect
Name some intrinsic RBC defects
membrane defects
abnl Hb
Enzyme def
Name some extrinsic RBC defects
blood loss > 1 week
immune hemolytic anemia
micro/macroangiopathic hemolytic anemia
malaria
end product of Hb degradation in macrophage
unconjugated bilirubin
Primary Fe storage protein
ferritin
Primary storage site of ferritin
BM macrophages
Effect of inflammation on ferritin synthesized by macrophages
increased
Decreased serum ferritin is diagnostic of
Fe deficiency
Increased serum ferritin can indicate
anemia of chronic disease
Fe overload
Serum Fe is bound to
transferrin
organ that makes transferrin
liver
Normal serum Fe
100 ug/dL
TIBC correlates directly with
tranferrin levels
normal TIBC
300 ug/dL
effect of decreased ferritin on transferrin
increased synthesis
Formula for Fe saturation
Fe Sat = serum Fe/TIBC x 100
Fe sat represents
the percentage of binding sites on transferrin occupied by Fe
Normal Fe sat
33%
Dec Fe sat indicates
Fe def
anemia of chronic disease
inc Fe sat indicates
Fe overload
most common cause of Fe def anemia
bleed
Disease caused by chronic Fe deficiency
Plummer Vinson syndrome (esophageal web, achlorhydria, glossitis, spoon nails)
Fe def lab findings (MCV, serum Fe, Fe sat, ferritin, TIBC, RDW)
MCV dec
serum Fe dec
Fe sat dec
ferritin dec
TIBC inc
RDW inc
most common cause of blood loss in women < 50 years
menorrhagia
most common cause of blood loss in men < 50
PUD
Most common cause of blood loss in people > 50
polyps/colorectal ca
Most common cause of Fe def in young kids
decreased intake
Daily Fe requirement during preggo
3.4 mg/day
Daily Fe requirement during lactation
2.5-3mg/day
Sequence of Fe def
absent Fe stores
dec serum ferritin
dec serum Fe
inc TIBC
dec Fe sat
normocytic normochromic anemia
microcyto hypochromic anemia
Most common anemia in hospitalized pt's
anemia of chronic disease (ACD)
common causes of ACD
chronic inflammation
alcoholism
malignancy
most common causes of ACD
alcoholism and malignancy
relationship of hepcidin and ACD
acute phase reactant protein released by liver in response to inflammation --> enter macrophage --> prevent release of Fe to transferrin --> increased Fe stores in BM macros
Lab findings of ACD (MCV, serum Fe, TIBC, Fe sat, serum ferritin)
MCV dec
serum Fe dec
TIBC dec
Fe sat dec
serum ferritin inc
4 y-chains (Hb Bart) is assoc w/
a-thalassemia (4 a-gene deletions -/- -/-. Incompatible w/ life)
B-thal caused by DNA splicing defect tends to be
mild
B thal caused by stop codon tends to be
severe
B/B+ thal is which category of B thal?
minor
B thal minor characteristics
mild microcytic anemia
mild protection against falciparum malaria (due to shorter RBC life span)
dec MCV, Hb, Hct
inc RBC
nl RDW, serum ferritin
Dec HbA and inc HbA2/HbF in Hb electrophoresis
B0/B0 thal is known as
B thal major
Hb electrophoresis findings in B thal major
no HbA
inc HbA2
inc HbF
Clinical presentation of B thal maj
hemolytic anemia (a chain inclusions removed by macros in spleen = hemolysis = inc unconjugated Hb)
extramed EPOesis
inc RDW/retic
Tx B thal maj
long term transfusion
danger of long term blood transfusion
Fe overload (hemosiderosis)
Causes of sideroblastic anemia (SBA)
chronic alcoholism
pyridoxine def
Pb poison
most common cause of SBA
chronic alcoholism
pathogenesis of sideroblastic anemia
defective heme synth in mitochrondria = Fe accumulate in mito of young RBC's = ringed sideroblasts
what type of anemia is SBA?
Fe overload
Most common cause of B6 def
INH
Most common causes of Pb poisoning
paint
batteries
pathogenesis of Pb poisoning
denature ferrochelatase = can't bind Fe to protoporphyrin = accumulate protoporphyrin

denature ALA dehydrase = inc delta-ALA

denature ribonuclease = can't degrade ribosomes = persist in RBC = basophilic stippling
PE findings of Pb poisoning
abdominal colic + diarrhea (visible Pb on plain film)
encephalopathy (delta-ALA = neuron damage, inc vessel permeability, demyelination)
growth retardation in children (Pb deposit in epiphysis of growing bones)
periph neuropathy in adults (foot drop, etc)
nephrotoxicity (Fanconi's syndrome = prox tubular acidosis, aminoaciduria, phosphaturia, glucosuria)
Inc whole blood and urine Pb levels
Best screening/confirmatory test for Pb poisoning
blood/urine Pb
Lab findings of sideroblastic anemia
inc serum Fe, Fe sat, ferritin
dec MCV, TIBC
BM aspirate = ringed sideroblasts
Most common cause of macrocytic anemia
folate or B12 def
B12 malabsorption due to
dec IF (ie pernicious anemia)
dec gastric acid (can't activate pepsinogen to release B12)
dec GI reabsorption (any destruction of terminal ileum, bact overgrowth, fish tapeworm, chronic pancreatitis = can't cleave off R-binder)
who's more likely to be deficient in B12: pure vegan, elderly, or pregnant/lactating?
pure vegan
most common cause of folate def
dec intake
most common cause of inc homocysteine
folate def
effect of inc homocysteine
endothelial cell damage --> thrombosis
Distinguish between folate def and B12 def anemia
B12 def has neuro problems
someone with an enlarged, smooth, red tongue, hx of alcoholism, and poor diet will most likely show what on microscopic exam of blood?
macrocytosis w/ basophilic stippling
hypersegmented neutrophils
low retic count
Most common METABOLIC disorder of RBCs
G6PD def
G6PD def lab values for
periph smear
CBC
retic
haptoglobin
Coombs
periph smear - schistocytes, microcytosis, Heinz bodies
CBC- anemia, reticulocytosis
haptoglobin - low
Coombs - neg
Things that bring out G6PD def
oxidative stress (sulfa drugs, infection, DKA, etc)