Incidental finding of rare hemoglobin: hemoglobin Bari in northeast Spain.

OBJECTIVES

Cation exchange high-performance liquid chromatography (HPLC) is one of the techniques available for determining glycated hemoglobin (HbA) and also the method of choice for structural hemoglobinopathies screening. The objective of this case is to show how in a routine HbA test it is possible to incidentally find a hemoglobinopathy.

CASE PRESENTATION

In a routine blood analysis, an abnormal value for the hemoglobin A2 (HbA) was obtained during the study of HbA with HPLC on the ADAMS™ A1c HA-8180T. After suspecting it could be due to the presence of a hemoglobinopathy, the study of possible variants was expanded using electrophoresis and HPLC on the Hydrasys and Variant II analysers, respectively. Since it could not be identified by these conventional methods, a genetic study was also carried out using Sanger sequencing. The patient presented a low HbA (1.3 %) and a 24.9 % variant with a retention time of 1.95 min, compatible with alpha-globin chain variant. In the genetic study, the pathogenic variant c.138C>G was detected in the  gene in heterozygosis, which resulted in the expression of the structural hemoglobinopathy known as hemoglobin Bari.

CONCLUSIONS

The initial screening for structural hemoglobinopathies allows its identification or suspicion especially when it was performed with HbA analysis, requiring subsequent confirmation and diagnosis by other techniques.