Hemolytic anemia is a modular concept, includes a variety of Pathology, a common symptom of which is increased destruction of red blood cells in the bloodstream, that leads, in turn, to the development of anemia, bilirubinemii and strengthen eritropoaiza. Among all the diseases of blood hemolytic anemia make up a little more 5%, among all anemias- 11,5%.
Among the hereditary causes include: congenital jeritropojeticheskaja Porphyria, hereditary sferocitoz, jelliptocitoz, deficiency of CH-6-dehydrogenase, Thalassemia, serpovidnokletochnaya anemia, carrier stable abnormal Hb, etc. Among the acquired causes include:
Regardless of the etiology of hemolysis, in the development of hemolytic anemia can be divided into three stages (hemolytic crisis, subcompensation hemolysis and remission). Haemolytic crisis characterized by the clinical manifestations of the anaemic syndrome and syndrome of bilirubin intoxication. When bilirubin intoxication appear nausea, vomiting, ikterichnost' skin and mucous membranes (especially skler), dizziness, headache, stomach ache, fever, and sometimes convulsions, disorders of consciousness. For the anaemic syndrome is characterized by weakness, dizziness, breathlessness, paleness of the skin and mucous membranes, tachycardia, expanding the boundaries of the heart, gluhost' heart tones, systolic murmur at the apex. Gradually increases the liver and spleen.
In the diagnosis of hemolytic anemias apply general blood test (detects anemia and changes the size and shape of red blood cells), biochemical blood analysis (including serum bilirubin, ALT, LDH), serum haptoglobin, urine hemoglobin and hemosiderin. To confirm the diagnosis can use bone marrow puncture (in the biopsy identifies active processes erythropoiesis).
The most characteristic for an intravascular hemolysis is active sferocitoz erythrocytes (in transfusion reactions, ancestral sferocitoze, When heat antibody hemolytic anemia). May also be shistocitoz (When intravaskuljarnom prosthetics, mikroangiopatiah), sickle-shaped red blood cells (when sickle-cell anemia), mishenevidnye erythrocytes (in liver pathologies, gemoglobinopatiâh), jadrosoderzhashhie erythrocytes and basophilia (high beta-tallasemii). Taurus Gejnca are detected when an unstable hemoglobin, Activation peroxide oxidation, akantocity-with anemia with shporovidnymi cell, aggljutinirovannye cells with cold agglutinin disease.
Congenital (hereditary) forms of hemolytic anemia can be divided into:
Acquired forms of hemolytic anemias are classified in:
Other hemolytic anemia-idiopathic (in half the cases), secondary (lymphomas) anemia, hemolytic jaundice of newborn.
If you suspect the presence of anemia are referred to a specialist.
For the treatment of hemolytic anemias glukokorticosteroida used, immunosuppressants, transfusion of washed red blood cells, piracetam (in the complex therapy), they can also conduct splenjektomiju (removal of the spleen).
The only possible way to prevent the development of anemia is maintaining a healthy lifestyle, timely treatment and prevention of other diseases.
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