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CC BY-NC-ND 4.0 · J Lab Physicians 2017; 9(04): 332-336
DOI: 10.4103/JLP.JLP_95_17
Case Report

Rare presentation of mixed autoimmune hemolytic anemia in children: Report of 2 cases

Preeti Rai
Department of Pathology, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India
,
Geetika Sharma
Department of Pathology, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India
,
Deeksha Singh
Department of Pathology, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India
,
Jyoti Garg
Department of Pathology, Lady Hardinge Medical College and Associated Hospitals, New Delhi, India
› Institutsangaben Financial support and sponsorship Nil.
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Abstract

Immune hemolytic anemia is characterized by clinical and laboratory features of hemolytic anemia with direct antiglobulin test (DAT) positivity. It could be autoimmune hemolytic anemia (AIHA), alloimmune, or drug-induced hemolysis based on the antigenic stimulus. Furthermore, based on thermal amplitude of autoantibody, AIHA is classified as warm (65%), cold (30%), and mixed (5%) type. Mixed AIHA is extremely rare in children and must be differentiated from warm AIHA with clinically insignificant cold agglutinins and cold hemagglutinin disease as their treatment is different. It may present as blood group discrepancy or cross-match incompatibility leading to delay in arranging suitable blood unit for transfusion. Therefore, a thorough immunohematology workup including monospecific DAT, indirect antiglobulin test at 4°C and 37°C, determination of thermal amplitude and titer is essential. We hereby present two pediatric cases of mixed AIHA presenting as ABO forward and reverse blood group discrepancy and cross-match incompatibility.

Key words

Autoantibody - autoimmune hemolytic anemia - best match blood - direct antiglobulin test - transfusion


Publikationsverlauf

Eingereicht: 23. Mai 2017

Angenommen: 21. Juni 2017

Artikel online veröffentlicht:
19. Februar 2020

© 2017.

Thieme Medical and Scientific Publishers Private Ltd.
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