Hemolytic anemia classification: Difference between revisions
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*Transfusion of blood from a donor with a different blood type | *Transfusion of blood from a donor with a different blood type | ||
Hemolytic anemias can be either genetic or acquired. | '''Hemolytic anemias can be either genetic or acquired.''' | ||
===Genetic=== | ===Genetic=== |
Revision as of 16:11, 28 August 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Classification
Types of Hemolytic Anemias
- Secondary immune hemolytic anemia
- Idiopathic autoimmune hemolytic anemia
- Non-immune hemolytic anemia caused by chemicals or toxins
- Microangiopathic hemolytic anemia (MAHA)
- Sickle-cell anemia
- Hemoglobin SC disease (similar in symptoms to sickle-cell anemia)
- Thalassemia
- Hemolytic anemia due to G6PD deficiency
- Paroxysmal nocturnal hemoglobinuria (PNH)
- Hereditary elliptocytosis
- Hereditary ovalocytosis
- Hereditary spherocytosis
- Malaria
- Transfusion of blood from a donor with a different blood type
Hemolytic anemias can be either genetic or acquired.
Genetic
- Genetic conditions of RBC membrane
- Genetic conditions of RBC metabolism (enzyme defects)
- Glucose-6-phosphate dehydrogenase deficiency (G6PD or favism)
- Pyruvate kinase deficiency
- Genetic conditions of hemoglobin
Acquired
Acquired hemolytic anemia can be further divided into immune and non-immune mediated.
Immune mediated hemolytic anaemia (direct Coombs test is positive)
- Autoimmune hemolytic anemia
- Warm antibody autoimmune hemolytic anemia
- Idiopathic
- Systemic lupus erythematosus (SLE)
- Evans' syndrome (antiplatelet antibodies and haemolytic antibodies)
- Cold antibody autoimmune hemolytic anemia
- Idiopathic cold hemagglutinin syndrome
- Infectious mononucleosis and mycoplasma ( atypical) pneumonia
- Paroxysmal cold hemoglobinuria (rare)
- Warm antibody autoimmune hemolytic anemia
- Alloimmune hemolytic anemia
- Haemolytic disease of the newborn (HDN)
- Rh disease (Rh D)
- ABO hemolytic disease of the newborn
- Anti-Kell hemolytic disease of the newborn
- Rhesus c hemolytic disease of the newborn
- Rhesus E hemolytic disease of the newborn
- Other blood group incompatibility (RhC, Rhe, Kidd, Duffy, MN, P and others)
- Alloimmune hemolytic blood transfusion reactions (ie from a non-compatible blood type)
- Haemolytic disease of the newborn (HDN)
- Drug induced immune mediated hemolytic anemia
- Penicillin (high dose)
- Methyldopa
Non-immune mediated hemolytic anemia (direct Coombs test is negative)
- Drugs (i.e., some drugs and other ingested substances lead to hemolysis by direct action on RBCs)
- Toxins (e.g., snake venom)
- Trauma
- Mechanical (heart valves, extensive vascular surgery, microvascular disease)
- Microangiopathic hemolytic anemia (a specific subtype with causes such as TTP, HUS, DIC and HELLP syndrome)
- Infections
- Membrane disorders
- Paroxysmal nocturnal hemoglobinuria (rare acquired clonal disorder of red blood cell surface proteins)
- Liver disease