RBC Morphologycontinued Hematology Review 302
ABNORMALITY DESCRIPTION SIGNIFICANCE
Target cells (codocytes)StomatocytesSpherocytesArrangement
RouleauxAgglutinationBull’s-eye, “Mexican hat cell”RBC with slit-like central pallorSmall, dark-staining RBCs without
central pallorRBCs resemble stack of coinsRBCs in irregular clumpsHemoglobinopathies, 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 autoagglutininDIC = disseminated intravascular coagulation
TTP = thrombotic thrombocytopenic purpura
HUS = hemolytic uremic syndrome