Evaluation of anemia
male: Hb<13
famale, children: Hb<11
new born: Hb<15
Morphology
macrocytic anemia: MCV>100, Vit. B12 or folic acid insufficiency, aplastic anemia, reticulocytosis, alcoholism, hypothyroidism, drug, other hematologic disease
normocytic anemia: MCV=80-100, uremia, endocrine disorder, leukemia, liver abscess
microcytic anemia: MCV<80, anemia of chronic disease, iron insufficiency, thalassemia
Reticulocyte productive index, RPI
RPI=Ret (%) X Hct / (45X maturation index)
Microcytic anemia
anemia of chronic disease
malignancy, chronic infection, chronic inflammation cause massive cytokine and hepcidin production and EPO production reduced
<Lab>
serum ferritin: ─/↑
serum iron: ↓
TIBC: ↓
transferrin saturation: ↓
Iron deficiency disease
most common, female predominal
<Lab>
serum ferritin: ↓
serum iron: ↓
TIBC: ↑
transferrin saturation: ↓
thalassemia
autosominal recessive, target cell or basophilic stippling in blood smear
alpha-thalassemia
1 alpha abnormal: carrier, no symptom
2 alpha abnormal: alpha thalassemia-minor, may disdiagnosised as iron deficiency anemia
3 alpha abnormal: alpha thalassemia-intermdiate=Hb H disease, jaundice, splenomegaly, hemochromatosis
4 alpha abnormal: alpha thalassemia-major=hydrops fetalis=Hb Bart's disease: unable to born
beta-thalassemia
1 beta abnormal: beta thalassemia-minor, no symptom or mild anemia
2 beta abnormal: beta thalassemia-major=Cooley's disease: Hb F>2% or Hb A2>3.5%, need transfusion to survive, and bone marrow transplant soon after birth
Macrocytic anemia
megaloblastic anemia
Vit. B12 or folic acid insufficiency, MCV>115, pancytopenia, reticulocyte↓, megaloblastic hyperplasia
* PANCYTO for pancytopenia: PNH, Aplastic anemia, Neoplasm, Cirrhosis,Y(Vit. B12 or folic acid), Toxin, Overwhelming sepsis
Aplastic anemia
Hb<10, neutrophil<1500, platelet<50K, autoimmune disease
* neutropenia: ANC(=WBC*(Seg%+band%)<1500/uL
* neutropenia: ANC(=WBC*(Seg%+band%)<1500/uL