1.Spectrin Tunis (Sp alpha I/78) in a Korean Family with Hereditary Elliptocytosis.
Eunhee HAN ; Ahhyun KIM ; Joonhong PARK ; Myungshin KIM ; Yonggoo KIM ; Kyungja HAN ; Yoo Jin KIM
Annals of Laboratory Medicine 2013;33(5):386-389
No abstract available.
Adult
;
Anemia/diagnosis
;
Asian Continental Ancestry Group/*genetics
;
Base Sequence
;
Bone Marrow Cells/cytology/pathology
;
Elliptocytosis, Hereditary/*diagnosis/*genetics/pathology
;
Female
;
Heterozygote
;
Humans
;
Infant, Newborn
;
Mutation, Missense
;
Republic of Korea
;
Spectrin/chemistry/*genetics
;
Splenomegaly/ultrasonography
2.Correction of Pseudoreticulocytosis in Leukocytosis Samples Using the Sysmex XE-2100 Analyzer Depends on the Type and Number of White Blood Cells.
Ahhyun KIM ; Joonhong PARK ; Myungshin KIM ; Jihyang LIM ; Eun Jee OH ; Yonggoo KIM ; Yeon Joon PARK ; Kyungja HAN
Annals of Laboratory Medicine 2012;32(6):392-398
BACKGROUND: The reticulocyte count is a good marker of erythropoietic activity of the bone marrow. In the mid-1990s, automated flow cytometric analysis replaced microscopy for the quantification of reticulocytes. Leukocytosis cases with an erroneously high reticulocyte count and a high immature reticulocyte fraction (IRF) have been reported. In this study, we analyzed reticulocyte counts in leukocytosis samples, in an effort to identify a correction method. METHODS: The study comprised of 21 samples from 16 leukocytosis patients. Results of reticulocyte analyses obtained using a XE-2100 hematology analyzer (Sysmex, Japan) were compared with those obtained using the supravital staining technique, which is a reference method. If the samples showed erroneously high reticulocyte counts and IRF, they were reanalyzed after serial dilution with isotonic solution. RESULTS: Five samples from 4 patients showed erroneously elevated reticulocyte counts and/or IRF on the XE-2100 analyzer. They displayed abnormal reticulocyte scattergrams, with 4 of 5 cases indicated by a flag. The white blood cell (WBC) fractions overlapped with the reticulocyte regions, especially with the IRF. Diagnoses and blast counts were variable when such errors occurred; WBC counts varied from 218.19x10(9)/L to 725.14x10(9)/L. The errors were corrected by simple dilution with isotonic solution. However, the corrective WBC counts differed according to individual cases. CONCLUSIONS: When leukocytosis samples exhibit an abnormal reticulocyte scattergram with a flag, or an abnormally high IRF, we recommend the dilution of the sample with isotonic solution to a WBC count of about 100.00x10(9)/L, followed by reanalysis of the reticulocyte count and reticulocyte scattergram.