Hemolytic anemia: Difference between revisions

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** Direct antiglobulin ("Coombs") test-negative
** Direct antiglobulin ("Coombs") test-negative
** Direct antiglobulin ("Coombs") test-positive
** Direct antiglobulin ("Coombs") test-positive
** Cold agglutinin disease<ref name="pmid22330255">{{cite journal| author=Berentsen S, Tjønnfjord GE| title=Diagnosis and treatment of cold agglutinin mediated autoimmune hemolytic anemia. | journal=Blood Rev | year= 2012 | volume= 26 | issue= 3 | pages= 107-15 | pmid=22330255 | doi=10.1016/j.blre.2012.01.002 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22330255  }} </ref>
* Complement-induced lysis
* Complement-induced lysis
* [[Microangiopathic hemolytic anemia]]. Includes [[Thrombotic thrombocytopenic purpura]].
* [[Microangiopathic hemolytic anemia]]. Includes [[Thrombotic thrombocytopenic purpura]].

Revision as of 00:22, 22 December 2014

In hematology, Hemolytic anemia is an "A condition of inadequate circulating red blood cells (anemia) or insufficient hemoglobin due to premature destruction of red blood cells (erythrocytes)."[1]

Classification

One classification is based on whether hemolysis occurs intravascularly or extravascularly. Another classification is whether the erythrocytes are intrinsically normal:[2]

Hemolytic anemia associated with normal red cells

Hemolytic anemia associated with abnormal red cells

Diagnosis

Hemolysis

Autoimmunity:

References