Hemolytic anemia causes: Difference between revisions
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===Extrinsic factors=== | ===Extrinsic factors=== | ||
* Commonly acquired in nature | * Commonly acquired in nature | ||
* Immune system abnormality | * Immune system abnormality. Antibodies against RBC membrane such as autoimmune hemolytic anemia, alloimmune hemolytic anemia, delayed [hemolytic] transfusion reaction, some drug-induced hemolytic anemias) | ||
* Blood clots in small blood vessels | * Blood clots in small blood vessels | ||
* Infections | * Infections |
Revision as of 18:16, 25 September 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
It has numerous possible causes, ranging from relatively harmless to life-threatening.
Causes
Common Causes
- Hemolytic anemia occurs when the bone marrow is unable to increase production to make up for the premature destruction of red blood cells.
- If the bone marrow is able to keep up with the early destruction, anemia does not occur (this is sometimes called compensated hemolysis).
- There are many types of hemolytic anemia, which are classified by the reason for the premature destruction of red blood cells. The defect may be in the red blood cell itself (intrinsic factors), or outside the red blood cell (extrinsic factors).
Intrinsic or Intracorpuscular
- Commonly hereditary in nature exceptions, paroxysmal nocturnal hemoglobinuria and acquired alpha thalassemia
- Occurs secondary to abnormalities in RBC components such as hemoglobin, RBC membranes (alpha or beta globin chains in thalassemia, hereditary spherocytosis, paroxysmal nocturnal hemoglobinuria), glycolysis, and reducing power of the RBC.
Extrinsic factors
- Commonly acquired in nature
- Immune system abnormality. Antibodies against RBC membrane such as autoimmune hemolytic anemia, alloimmune hemolytic anemia, delayed [hemolytic] transfusion reaction, some drug-induced hemolytic anemias)
- Blood clots in small blood vessels
- Infections
- Medications side-effects