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Microcytic, Hypochromic Anemias Hematology Review 311


ANEMIA ETIOLOGY BLOOD SMEAR OTHER

Iron deficiency
anemia (IDA)

Sideroblastic anemia

b–thalassemia major

b–thalassemia minor

Anemia of chronic
inflammation*

Insufficient iron for hgb
synthesis.

Enzymatic defect in heme
synthesis.

↓b-chain production.

↓b-chain production.

Acute phase reactants (e.g.,
hepcidin) affect iron absorp-
tion & release. Iron in bone
marrow macrophages is not
released to developing RBCs.

Aniso, poik, hypochromic
microcytes

Dual population of RBCs
(normocytic & microcytic),
Pappenheimer bodies,
basophilic stippling

Marked aniso & poik,
hypochromic microcytes,
target cells, ovalocytes,
nRBCs, basophilic stippling

Aniso, poik, hypochromic
microcytes, target cells,
basophilic stippling

60%–70% of cases have
normocytic normochromic
RBCs; 30%–40% microcytic
hypochromic

Most common anemia.

RBC indices usually normal.
Ringed sideroblasts in marrow.

Homozygous. Little or no Hgb A,
95%–98% F, 2%–5% A 2.
Severe anemia. MCV <67 fL.

Heterozygous. >90%–95% Hgb A,
3.5%–7% A 2 , 2%–5% F.
Mild anemia.

Associated with chronic infections &
inflammation, malignancies, autoim-
mune diseases. 2nd most common
anemia after IDA. Most common
anemia in hospitalized pts.

*Formerly known as anemia of chronic disease. More often normocytic normochromic but included here because must be considered in differential Dx of microcytic anemia.

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