Autoimmune hemolytic anemia: Difference between revisions

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== See Also ==
== See Also ==
* [[Anemia]]
* [[Anemia]]
* [[Immune System Disorders]]
* [[Immune system disorders]]
* [[Blood Disorders]]
* [[Blood disorders]]
 
== References ==
== References ==
<references />
<references />

Latest revision as of 02:52, 14 May 2025

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Autoimmune hemolytic anemia
Synonyms AIHA
Pronounce N/A
Specialty N/A
Symptoms Fatigue (medical), pallor, jaundice, shortness of breath, tachycardia
Complications Heart failure, splenomegaly, thrombosis
Onset Any age, but more common in adults
Duration Variable
Types N/A
Causes Autoimmune disease, idiopathic, drug-induced
Risks Systemic lupus erythematosus, chronic lymphocytic leukemia, HIV/AIDS
Diagnosis Coombs test, complete blood count, blood smear
Differential diagnosis Hereditary spherocytosis, G6PD deficiency, cold agglutinin disease
Prevention N/A
Treatment Corticosteroids, immunosuppressive drugs, splenectomy, blood transfusion
Medication Prednisone, rituximab
Prognosis Variable; depends on underlying cause and response to treatment
Frequency Rare
Deaths N/A


Autoimmune hemolytic anemia (AIHA), is a medical condition wherein the body's own immune system mistakenly attacks and destroys red blood cells, leading to anemia. This condition can be acute or chronic and can range from mild to severe.

Introduction[edit]

AIHA occurs when the body produces antibodies that specifically target its own red blood cells. These antibodies can cause the red blood cells to burst (hemolyze) or can result in their premature removal by the spleen or liver.

Causes[edit]

There are a number of reasons why AIHA might develop, including:

  • Underlying diseases or conditions, such as lupus or certain types of cancer.
  • Certain medications.
  • After a viral infection.
  • Due to genetic predisposition.
  • Unknown causes - termed as idiopathic.

Types of AIHA[edit]

AIHA can be categorized based on the temperature at which the antibodies are most active:

  • Warm AIHA: This is the most common type, where antibodies act best at body temperature. They can be idiopathic or related to an underlying condition.
  • Cold AIHA: Here, antibodies are active at colder temperatures, often triggered after exposure to cold environments.

Symptoms[edit]

Patients with AIHA might exhibit various symptoms, including:

  • Fatigue and weakness.
  • Pale or yellowish skin.
  • Dark urine.
  • Rapid heartbeat or shortness of breath.
  • Enlarged spleen.

Treatment[edit]

The treatment for AIHA often involves:

  • Stopping any medication causing the anemia.
  • Corticosteroids to suppress the immune response.
  • Immune suppression drugs.
  • Blood transfusions in severe cases.
  • Surgical removal of the spleen in some situations.

See Also[edit]

References[edit]

<references />




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