RBC Morphologycontinued Hematology Review 302
ABNORMALITY DESCRIPTION SIGNIFICANCE
Target cells (codocytes)
Stomatocytes
Spherocytes
Arrangement
Rouleaux
Agglutination
Bull’s-eye, “Mexican hat cell”
RBC with slit-like central pallor
Small, dark-staining RBCs without
central pallor
RBCs resemble stack of coins
RBCs in irregular clumps
Hemoglobinopathies, thalassemia, liver disease. May be
artifact if observed in only 1 part of smear.
Hereditary stomatocytosis, hereditary spherocytosis, tha-
lassemia, alcoholic cirrhosis, Rh null disease. May be artifact
in parts of smear that are too thin or too thick.
Membrane defect. Hereditary spherocytosis, autoantibodies,
burns, hemoglobinopathies, hemolysis, ABO HDN, incompat-
ible blood tf, tf of stored blood. A few are normal due to
aging of RBCs.
Serum protein abnormality; e.g., ↑globulins or fibrinogen.
Seen in multiple myeloma & macroglobulinemia. May be
artifact due to delay in spreading drop of blood or smear
that’s too thick.
Autoantibodies, cold autoagglutinin
DIC = disseminated intravascular coagulation
TTP = thrombotic thrombocytopenic purpura
HUS = hemolytic uremic syndrome