Autoimmune hemolytic anemia
From IDWiki
Differential Diagnosis
- Cold AIHA
- Primary: cold agglutinin disease (CAD)
- Secondary
- Viral infections: EBV, CMV, others
- Other infections: Mycoplasma (paroxysmal cold hemoglobinuria)
- Other diseases: Waldenström macroglobulinema, lymphoma
- Drugs: lenalidomide
- Warm AIHA
- Primary: warm AIHA
- Secondary
- Viral infections: HIV, vaccines
- Other diseases: lupus, CLL and other malignancies, chronic inflammatory disorders (including IBD)
- Allogeneic hematopoietic stem cell transplantation
- Drugs: cefotetan, ceftriaxone, piperacillin, immune checkpoint-modulating drugs (e.g. nivolumab)
- Drug-related
Management
Warm AIHA
- Can be an emergency if severe and acute
- If life-threatening, transfuse ABO-matched but incompatible blood, thereby sparing the patient's own cells
- First-line: prednisone 1 mg/kg daily (response in 50% of patients)
- Second-line: rituximab 100 mg/week for 4 weeks, with prednisone
- Refractory: splenectomy
Cold agglutinin disease
- Chronic hemolysis in older patients caused by IgM antibodies produced by a B-lymphocyte clone (can show up as MGUS), therefore is essentially a form of Waldenström macroglobulinema
- First-line: rituximab ± fludarabine
- Prednisone and splenectomy are not helpful