Table 1

Characteristics of patients with spontaneous mixed RhD phenotype

PatientSexAge, y*DiagnosisRH genotypeBlood group phenotype
D-positive RBCs, %Number of D sites per D-positive RBCs§Follow-up, moDynamics of D antigen positivity over follow-up interval
RhDuffy
DCEceFyaFyb
63 Idiopathic osteomyelofibrosis CcDdee ± ± − 56 11182 44 Complete loss 
56 Rheumatoid arthritis CcDdee ± ± − − 67 12073 52 Stable 
60 Anal fistula CcDdee ± ± − − 46 12578 40 Stable 
86 Essential thrombocythemia CcDdee ± ± − − 85 9838 Stable 
33 Uterus myomatosus CcDdee ± ± − ± 81 11380 24 Stable 
67 Acute myelogenous leukemia CcDvardee ±w ± − − 56 4419 13 Progressive loss 
43 Psychosis ccDdEe ± − ± 22 nd 65 Progressive loss 
78 Colon carcinoma CcDdee ± ± − − nd nd 33 Complete loss 
86 Leg vein thrombosis CcDdee ± ± − − 40 10950 12 Stable 
PatientSexAge, y*DiagnosisRH genotypeBlood group phenotype
D-positive RBCs, %Number of D sites per D-positive RBCs§Follow-up, moDynamics of D antigen positivity over follow-up interval
RhDuffy
DCEceFyaFyb
63 Idiopathic osteomyelofibrosis CcDdee ± ± − 56 11182 44 Complete loss 
56 Rheumatoid arthritis CcDdee ± ± − − 67 12073 52 Stable 
60 Anal fistula CcDdee ± ± − − 46 12578 40 Stable 
86 Essential thrombocythemia CcDdee ± ± − − 85 9838 Stable 
33 Uterus myomatosus CcDdee ± ± − ± 81 11380 24 Stable 
67 Acute myelogenous leukemia CcDvardee ±w ± − − 56 4419 13 Progressive loss 
43 Psychosis ccDdEe ± − ± 22 nd 65 Progressive loss 
78 Colon carcinoma CcDdee ± ± − − nd nd 33 Complete loss 
86 Leg vein thrombosis CcDdee ± ± − − 40 10950 12 Stable 

RBC indicates red blood cell; ±, positive/negative mixed-field agglutination; −, negative; +, positive; ± w, weak positive/negative mixed-field; and nd, not determined.

*

Age at initial recognition of mixed RhD status.

RH genotype and RHD zygosity as determined from blood DNA samples.

In all patients, normal unmixed ABO, MNS, P, Lutheran, Kell, and Kidd blood group phenotypes were found.

§

D antigen densities of RH genotype–matched CcDdee and CcDvardee (D category IV type 4) control samples were 10724 and 4327 D sites per red cell, respectively.

Time interval from initial serologic recognition of mixed RhD status to its latest determination; during this time, no patient received transfusions.

Patient 6 (CcDvardee) displayed a partial D variant, D category IV type 4.

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