Warm-reacting-antibody hemolytic anemia
Warm-reacting-antibody hemolytic anemia is a type of autoimmune hemolytic anemia (AIHA) characterized by the presence of antibodies that react at body temperature, leading to the destruction of red blood cells. This condition is one of the most common forms of AIHA and can be idiopathic or secondary to other conditions such as lupus, chronic lymphocytic leukemia, or certain infections.
Causes[edit | edit source]
Warm-reacting-antibody hemolytic anemia is caused by the immune system mistakenly producing antibodies against the body's own red blood cells. These antibodies attach to the red blood cells at body temperature and mark them for destruction, primarily in the spleen. The exact trigger for the production of these antibodies is unknown in idiopathic cases, but the condition can also arise secondary to other diseases or exposure to certain drugs.
Symptoms[edit | edit source]
Symptoms of warm-reacting-antibody hemolytic anemia can vary from mild to severe and may include fatigue, pallor, jaundice, an increased heart rate, shortness of breath, and dark-colored urine. The severity of symptoms generally correlates with the rate of red blood cell destruction.
Diagnosis[edit | edit source]
Diagnosis involves a combination of clinical evaluation and laboratory tests. Key tests include a complete blood count (CBC), which often shows anemia with an increased reticulocyte count, and a direct antiglobulin test (DAT, also known as the Coombs test), which is positive for antibodies or complement on the surface of red blood cells. Additional tests may be performed to determine the underlying cause if the condition is suspected to be secondary.
Treatment[edit | edit source]
Treatment of warm-reacting-antibody hemolytic anemia focuses on reducing the immune system's attack on red blood cells. First-line therapy typically involves corticosteroids to suppress the immune system. In cases where corticosteroids are ineffective or not tolerated, other treatments such as immunosuppressive drugs, rituximab, or splenectomy (removal of the spleen) may be considered. Treatment also includes supportive care, such as folic acid supplementation and possibly blood transfusions.
Prognosis[edit | edit source]
The prognosis for individuals with warm-reacting-antibody hemolytic anemia varies. Some patients respond well to initial treatment and may achieve long-term remission, while others may have a chronic condition requiring ongoing management. Secondary forms of the disease may resolve if the underlying condition is effectively treated.
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Contributors: Prab R. Tumpati, MD