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Severe immune hemolytic anemia associated with warm-reacting IgM autoantibodies: a diagnostic (and therapeutic) challenge (CROSBI ID 692843)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Raos, Mirela ; Lukic, Marija ; Burnac, Iva Lucija ; Plenkovic, Fini ; Aurer, Igor ; Golubic Cepulic, Branka Severe immune hemolytic anemia associated with warm-reacting IgM autoantibodies: a diagnostic (and therapeutic) challenge // Vox Sanguinis. 2016. str. 222-222

Podaci o odgovornosti

Raos, Mirela ; Lukic, Marija ; Burnac, Iva Lucija ; Plenkovic, Fini ; Aurer, Igor ; Golubic Cepulic, Branka

engleski

Severe immune hemolytic anemia associated with warm-reacting IgM autoantibodies: a diagnostic (and therapeutic) challenge

Autoimmune hemolytic anemia (AIHA) can present with severe intraand extravascular hemolysis. In warm AIHA (WAIHA), characterised by IgG autoantibodies, hemolysis is tipically extravascular ; however, complement-mediated intravascular hemolysis can be seen in “mixed” type AIHA, characterised by both IgG warm autoantibodies and IgM cold autoantibodies reactive up to 30 to 37°C, and in rare WAIHA caused by IgM warm autoantibodies. Diagnostic of IgM WAIHA is very difficult. It can be confused with cold agglutinin syndrome, caused by IgM cold autoantibodies reactive up to 30°C or with “mixed” type AIHA. Although death from WAIHA is considered rare (4–11%), it is particularly high (22%) in IgM WAIHA.

Immune hemolytic anemia, warm-reacting IgM autoantibodies

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Podaci o prilogu

222-222.

2016.

objavljeno

Podaci o matičnoj publikaciji

Vox Sanguinis

Podaci o skupu

34th International Congress of the ISBT

poster

03.09.2016-08.09.2016

Dubai, Ujedinjeni Arapski Emirati

Povezanost rada

nije evidentirano