Hemolytic Anemias

Hemolytic anemia

Definition

Hb < 12 g/dL (F) or < 13 g/dL (M) typically associated with elevated reticulocyte count and positive hemolytic markers, including:

  • Increased LDH
  • Increased indirect bilirubin
  • Increased AST
  • Decreased haptoglobin

Differential diagnosis

  • Immune:
    • Autoimmune:
      • Warm autoimmune hemolytic anemia
      • Cold autoimmune hemolytic anemia (cold agglutinin disease)
    • Alloimmune:
      • Immediate transfusion reaction
      • Delayed transfusion reaction
  • Non-immune:
    • Intracorpuscular:
      • Hemoglobinopathy:
        • Sickle cell disease
        • Thalassemia
      • Membranopathy:
        • Hereditary spherocytosis
        • Hereditary elliptocytosis
      • Enzymopathy:
        • G6PD deficiency
        • Pyruvate kinase deficiency
    • Extracorpuscular:
      • Thrombotic microangiopathy
      • Valve hemolysis
      • March hemoglobinuria
      • Spur cell anemia
      • Zieve syndrome
      • Wilson disease
      • Infection
        • Babesiosis
        • Malaria
        • C. perfringens
      • Thermal injury
  • Other conditions associated with positive hemolytic markers:
    • Resorbing hematoma
    • HLH
    • Pernicious anemia

 

 

Peripheral smear findings

ConditionFindings
Warm autoimmune hemolytic anemiaSize
+/- Microcytosis
Anisocytosis (from spherocytes + reticulocytes)
Staining
Hyperchromia (loss of central pallor)
Increased polychromatophilic cells
Shapes
Spherocytes
Inclusions
Typically none
Cold agglutinin diseaseSize
Normal
Staining
Mostly normochromic
Increased polychromatophilic cells
Shapes
Normal
Inclusions
Typically none
Other:
RBC agglutination
Sickle cell diseaseSize
Normal
Staining
Loss of central pallor in sickle forms
Increased polychromatophilic cells
Shapes
Irreversibly sickled cells
Boat cells
Inclusions
Nucleated RBCs
Howell-Jolly bodies
Basophilic stippling
Hereditary spherocytosisSize
+/- Microcytosis
Anisocytosis (from spherocytes + reticulocytes)
Staining
Hyperchromia (loss of central pallor)
Increased polychromatophilic cells
Shapes
Spherocytes
Inclusions
Typically none
Thrombotic microangiopathySize
Typically normal
Staining
Normal central pallor
Increased polychromatophilic cells
Shapes
Schistocytes
Inclusions
Typically none

Examples of peripheral smear findings

  • Warm autoimmune hemolytic anemia
  • Cold agglutinin disease
  • Thrombotic microangiopathy
  • Sickle cell disease

Additional TBP resources

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