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Comparison of paroxysmal cold hemoglobinuria, cold agglutinin disease, and cryoglobulinemia

Comparison of paroxysmal cold hemoglobinuria, cold agglutinin disease, and cryoglobulinemia
  Paroxysmal cold hemoglobinuria Cold agglutinin disease Cryoglobulinemia
Presentation
  • Typically in childhood, rarely adults
  • Dark (red-brown) urine after cold exposure with fever, chills, back or leg pain
  • Typically in older women (over 70 years)
  • Anemia symptoms, acrocyanosis
  • Typically in older individuals (over 60 years)
  • Palpable purpura, arthralgias, myalgias, may be chronic for decades
Associated diseases
  • Secondary or tertiary syphilis
  • Post-viral infection (eg, varicella, measles, mumps, EBV, CMV)
  • Post-bacterial infection (eg, mycoplasma, Klebsiella, Escherichia coli, Haemophilus influenzae)
  • Post-measles vaccine
  • Autoimmune disorders
  • Lymphoma or CLL
  • Lymphoma or other lymphoproliferative disorder
  • Infection (eg, mycoplasma, infectious mononucleosis)
  • Monoclonal IgM gammopathy
  • Autoimmune disorders
  • Infections (eg, adenovirus, hepatitis viruses, HIV, bacteria, spirochetes, fungi, parasites)
  • Autoimmune disorders
  • Inflammatory bowel disease
  • Neoplasms (various)
  • Lymphoproliferative disorders
  • Cirrhosis
  • Vaccinations
  • Familial syndromes
Clinical findings
  • Jaundice
  • Hemoglobinemia, hemoglobinuria, and hemosiderinuria
  • Raynaud phenomenon
  • Urticaria
  • Anemia
  • Neutropenia (rare)
  • Anemia
  • Livido reticularis
  • Acrocyanosis or Raynaud phenomenon
  • Fatigue, weakness, dyspnea
  • Hemoglobinuria (less common)
  • Dysphagia for cold foods/liquids
  • Small to medium vessel vasculitis
  • Macules, papules
  • Arthralgias/myalgias
  • Peripheral neuropathy
  • Raynaud phenomenon
Characteristics of hemolysis
  • Intravascular, biphasic
  • DAT positive using anti-C3 and negative using IgG, may be negative between episodes
  • Mainly extravascular; possibly intravascular in massive hemolytic crisis 
  • DAT positive using anti-C3 and negative using IgG (unless patient has an IgG, which may be warm-reacting)
  • Not associated with hemolysis
Characteristics of antibody
  • Antigen = "P antigen"
  • Cold-reacting IgG
  • Polyclonal
  • Does not cause RBC agglutination
  • Moderate titer (eg, <1:160)
  • Binds RBCs and fixes complement; causes hemolysis upon rewarming (Donath-Landsteiner antibody)
  • Antigen = "I" or "i" antigen
  • Cold-reacting IgM (rarely IgG or IgA)
  • Monoclonal or polyclonal
  • Agglutinates RBCs
  • High titer (eg, >1:2000)
  • Binds RBCs and fixes complement
  • Some cold agglutinins are also cryoglobulins
  • Mixture of antibodies and complement
  • Cold-reacting IgM, IgG, IgA, or combinations; may be isolated light chains, may be rheumatoid factor positive 
  • Monoclonal, polyclonal, or both
  • Concentration varies, measured in mg/dL
  • Precipitates upon cooling of plasma or serum
  • Complement may be consumed with immune complexes
  • Does not interact with RBCs
These clinical features are meant as a guide to typical findings and cannot be used in isolation to confirm or exclude a diagnosis. Refer to UpToDate content on paroxysmal cold hemoglobinuria, cold agglutinin disease, and cryoglobulinemia for further details.
PCH: paroxysmal cold hemoglobinuria; EBV: Epstein-Barr virus; CMV: cytomegalovirus; CLL: chronic lymphocytic leukemia; Ig: immunoglobulin; DAT: direct antiglobulin test (Coombs test); RBC: red blood cell.
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