Transfus Med Hemother. 2015 Sep;42(5):311-5. doi: 10.1159/000438960. Epub 2015 Aug 10.
Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie
Abdulgabar Salama
PMID: 26696799 PMCID: PMC4678313 DOI: 10.1159/000438960
Autoimmune haemolytic anaemias (AIHAs) are well-characterized disorders. They can be differentiated from one another and from other non-immune haemolytic anaemias by clinical, laboratory and serological testing. However, several misleading clinical presentations and/or serological findings may result in misinterpretation, delay and/or misdiagnosis. Such failures are avoidable by adequate clinical and serological experience of the responsible physicians and serologists or, at least, by an optimised bidirectional communication. As long as this has not been achieved, unpleasant failures are to be expected. A true diagnosis of AIHA can neither be verified by clinical nor serological findings alone. Thus, a collective clinical and serological picture remains obligatory for fulfilling the criteria of optimal diagnosis and therapy. Ultimately, the majority of pioneer scientific and practical work in this field stems from scientists who were simultaneously involved in both the clinic and serology.
Keywords: AIHA; Agglutination; Autoimmune haemolytic anaemia; C3d DAT; Coombs-negative; IgG DAT; Immune haemolysis; Negative DAT; Positive DAT