Autoimmune hemolytic anemia: Difference between revisions
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==Background== | ==Background== | ||
*Autoimmune hemolytic anemia (AIHA) = generation of auto-antibodies towards red blood cell membrane antigens, leady to hemolysis. | *Autoimmune [[hemolytic anemia]] (AIHA) = generation of auto-antibodies towards red blood cell membrane antigens, leady to hemolysis. | ||
*Can be primary ( | *Can be primary (idiopathic) or due to another disease process (e.g. malignancy, autoimmune disease, infection) | ||
==="Warm" Autoimmune Hemolytic Anemia=== | ==="Warm" Autoimmune Hemolytic Anemia=== | ||
''Autoantibodies agglutinate to RBCs at higher temperatures'' | ''Autoantibodies agglutinate to RBCs at higher temperatures'' | ||
*IgG mediated, usually pan-reactive to patient's and transfused RBCs | *IgG mediated, usually pan-reactive to patient's and transfused RBCs | ||
*Extravascular (i.e. in spleen) | *Extravascular (i.e. in spleen) hemolysis→ unconjugated > conjugated [[hyperbilirubinemia]] | ||
*Haptoglobin low, LDH may be normal | *Haptoglobin low, LDH may be normal | ||
*Causes: | *Causes: | ||
**[[Lymphoma]], especially Non-Hodgkin's lymphoma | **[[Lymphoma]], especially Non-Hodgkin's lymphoma | ||
**[[Leukemia]], particularly chronic lymphocytic leukemia | **[[Leukemia]], particularly [[chronic lymphocytic leukemia]] | ||
** Collagen vascular diseases (E.g. [[Systemic Lupus Erythematosus]], [[Rheumatoid arthritis]], [[Giant cell arteritis]] | **Collagen vascular diseases (E.g. [[Systemic Lupus Erythematosus]], [[Rheumatoid arthritis]], [[Giant cell arteritis]] | ||
**Viral-induced or [[HIV]]-associated | **Viral-induced or [[HIV]]-associated | ||
**Medications: methyldopa, quinidine, [[penicillin]] | **Medications: methyldopa, [[quinidine]], [[penicillin]] | ||
==="Cold" Autoimmune Hemolytic Anemia=== | ==="Cold" Autoimmune Hemolytic Anemia=== | ||
''Autoantibodies agglutinate at lower temperatures'' | ''Autoantibodies agglutinate at lower temperatures'' | ||
*IgM mediated | *IgM mediated | ||
*Intravascular | *Intravascular hemolysis→ high LDH, low haptoglobin, hemoglobinuria | ||
*Causes: | *Causes: | ||
**Infection, most commonly [[Mycoplasma pneumoniae]] and [[mononucleosis]], also [[varicella]], [[listeria]], [[influenza]] | **Infection, most commonly [[Mycoplasma pneumoniae]] and [[mononucleosis]], also [[varicella]], [[listeria]], [[influenza]] | ||
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*Signs/symptoms of underlying disease process | *Signs/symptoms of underlying disease process | ||
*Cold-type: | *Cold-type: | ||
**Acrocyanosis, Raynaud's, vascular occlusion with | **Acrocyanosis, [[Raynaud’s disease|Raynaud's]], vascular occlusion with peripheral tissue ischemia | ||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
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*Direct Coombs test - blood sample is removed of plasma and incubated with anti-human immunoglobulin (aka "Coombs reagent"). This detects if autoantibodies are attached to RBCs or compliment. If the RBCs are coated with IgG (positive direct Coombs test), this suggests the diagnosis of "warm AIHA. If the RBCs are coated with only compliment, this suggests the diagnosis of "cold" AIHA | *Direct Coombs test - blood sample is removed of plasma and incubated with anti-human immunoglobulin (aka "Coombs reagent"). This detects if autoantibodies are attached to RBCs or compliment. If the RBCs are coated with IgG (positive direct Coombs test), this suggests the diagnosis of "warm AIHA. If the RBCs are coated with only compliment, this suggests the diagnosis of "cold" AIHA | ||
== | ==Management== | ||
===Warm AIHA=== | ===Warm AIHA=== | ||
*Oral [[prednisone]] 1-1.5mg/kg/day for 1-3 weeks with taper after hemoglobin stable | *Oral [[prednisone]] 1-1.5mg/kg/day for 1-3 weeks with taper after hemoglobin stable | ||
**may need several months of low dose prednisone to remain in remission | **may need several months of low dose [[prednisone]] to remain in remission | ||
*Splenectomy and/or cytotoxic drugs for for steroid-refractory disease | *[[Splenectomy]] and/or cytotoxic drugs for for steroid-refractory disease | ||
* | *[[Plasmapheresis]] as temporizing measure for severe disease | ||
*Transfuse only if truly life-threatening anemia, least incompatible units possible | *Transfuse [[pRBCs]] only if truly life-threatening anemia, least incompatible units possible | ||
===Cold AIHA=== | ===Cold AIHA=== | ||
*No treatment for mild disease | *No treatment for mild disease | ||
*Immunosuppressive or cytotoxic medications can be considered | *Immunosuppressive or cytotoxic medications can be considered | ||
* | *[[Plasmapheresis]] for severe disease | ||
==Disposition== | ==Disposition== | ||
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*[[Rheumatoid arthritis]] | *[[Rheumatoid arthritis]] | ||
*[[Scleroderma]] | *[[Scleroderma]] | ||
==References== | |||
<references/> | |||
[[Category:Heme/Onc]] | |||
Latest revision as of 23:57, 30 September 2019
Background
- Autoimmune hemolytic anemia (AIHA) = generation of auto-antibodies towards red blood cell membrane antigens, leady to hemolysis.
- Can be primary (idiopathic) or due to another disease process (e.g. malignancy, autoimmune disease, infection)
"Warm" Autoimmune Hemolytic Anemia
Autoantibodies agglutinate to RBCs at higher temperatures
- IgG mediated, usually pan-reactive to patient's and transfused RBCs
- Extravascular (i.e. in spleen) hemolysis→ unconjugated > conjugated hyperbilirubinemia
- Haptoglobin low, LDH may be normal
- Causes:
- Lymphoma, especially Non-Hodgkin's lymphoma
- Leukemia, particularly chronic lymphocytic leukemia
- Collagen vascular diseases (E.g. Systemic Lupus Erythematosus, Rheumatoid arthritis, Giant cell arteritis
- Viral-induced or HIV-associated
- Medications: methyldopa, quinidine, penicillin
"Cold" Autoimmune Hemolytic Anemia
Autoantibodies agglutinate at lower temperatures
- IgM mediated
- Intravascular hemolysis→ high LDH, low haptoglobin, hemoglobinuria
- Causes:
- Infection, most commonly Mycoplasma pneumoniae and mononucleosis, also varicella, listeria, influenza
- Multiple myeloma and other plasmacytomas
- Idiopathic
Clinical Features
- Signs and symptoms of anemia (fatigue, pallor, palpitations, etc.)
- Jaundice and scleral icterus
- Signs/symptoms of underlying disease process
- Cold-type:
- Acrocyanosis, Raynaud's, vascular occlusion with peripheral tissue ischemia
Differential Diagnosis
Anemia
RBC Loss
RBC consumption (Destruction/hemolytic)
- Hereditary
- Acquired
- Microangiopathic Hemolytic Anemia (MAHA)
- Autoimmune hemolytic anemia
Impaired Production (Hypochromic/microcytic)
- Iron deficiency
- Anemia of chronic disease
- Thalassemia
- Sideroblastic anemia
Aplastic/myelodysplastic (normocytic)
Megaloblastic (macrocytic)
- Vitamin B12/folate deficiency
- Drugs (chemo)
- HIV
Evaluation
- CBC, LFTs, LDH, haptoglobin
- Direct Coombs test - blood sample is removed of plasma and incubated with anti-human immunoglobulin (aka "Coombs reagent"). This detects if autoantibodies are attached to RBCs or compliment. If the RBCs are coated with IgG (positive direct Coombs test), this suggests the diagnosis of "warm AIHA. If the RBCs are coated with only compliment, this suggests the diagnosis of "cold" AIHA
Management
Warm AIHA
- Oral prednisone 1-1.5mg/kg/day for 1-3 weeks with taper after hemoglobin stable
- may need several months of low dose prednisone to remain in remission
- Splenectomy and/or cytotoxic drugs for for steroid-refractory disease
- Plasmapheresis as temporizing measure for severe disease
- Transfuse pRBCs only if truly life-threatening anemia, least incompatible units possible
Cold AIHA
- No treatment for mild disease
- Immunosuppressive or cytotoxic medications can be considered
- Plasmapheresis for severe disease
Disposition
See Also
- Paroxysmal nocturnal hemoglobinuria (PNH)
- Systemic lupus erythematosus
- Rheumatoid arthritis
- Scleroderma