1. [Hemolytic anemias in adults].
- Author
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Müller A, Zimmermann R, and Krause SW
- Subjects
- Adult, Anemia, Hemolytic etiology, Anemia, Hemolytic, Autoimmune diagnosis, Coombs Test, Diagnosis, Differential, Hemoglobinuria etiology, Hemoglobinuria, Paroxysmal etiology, Hemolytic-Uremic Syndrome diagnosis, Humans, Purpura, Thrombotic Thrombocytopenic diagnosis, Anemia, Hemolytic diagnosis
- Abstract
The erythrocyte lifespan in haemolytic anemia is shortened while erythropoesis is increased. Important labaratory findings are increased reticulocytes, LDH, indirect bilirubin and a decreased haptoglobin level. The most important diagnostic tool for further work up of hemolytic anemia is the direct antiglobulin test (DAT, Coombs test) to differentiate autoimmune hemolytic anemia (AIHA) from other causes. Another important group are fragmentation syndroms (hemolytic uremic syndrome and thrombotic thrombocytopenic purpura). In these forms of haemolytic anemia fragmented red blood cells can be found in the blood smear together with thrombocytopenia. A severe problem in paroxysmal nocturnal hematuria is the incidence of thrombosis. The following review describes the most important forms of hemolytic anemia in the adult and the diagnostic and therapeutic strategies., (© Georg Thieme Verlag KG Stuttgart · New York.)
- Published
- 2011
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