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Summary
Cold agglutinins cause autoimmune hemolytic anemia, reacting most at low temperatures. This review details diagnosis for cold agglutination disease and paroxysmal cold hemoglobinuria.
Area of Science:
- Hematology
- Immunology
- Internal Medicine
Background:
- Cold autoimmune hemolytic anemia involves autoantibodies (cold agglutinins) reactive at low temperatures.
- The anti-I autoantibody is associated with cold hemagglutination disease and secondary anemias.
- Paroxysmal cold hemoglobinuria features the Donath-Landsteiner antibody, causing hemolysis upon cold exposure.
Observation:
- Anti-I cold agglutinins are prevalent in cold hemagglutination disease, lymphomas, leukemias, and atypical pneumonia.
- Infectious mononucleosis and other lymphoproliferative disorders can also present with anti-I antibodies.
- The Donath-Landsteiner antibody is a unique biphasic autoantibody specific to paroxysmal cold hemoglobinuria.
Findings:
- This article reviews cold autoimmune hemolytic anemias, focusing on cold agglutinins and the Donath-Landsteiner antibody.
- Diagnostic approaches for various cold autoimmune hemolytic anemias are presented.
- Table 4 provides a practical diagnostic strategy for autoimmune hemolytic anemias.
Implications:
- Understanding cold agglutinin types aids in diagnosing specific autoimmune hemolytic anemias.
- Differentiating between cold agglutinin disease and paroxysmal cold hemoglobinuria is crucial for appropriate management.
- This review serves as a practical guide for clinicians managing patients with autoimmune hemolytic anemias.