RETICULOCYTOGRAM IN PATIENTS WITH SICKLE CELL ANEMIA AND HEMOGLOBIN SC DISEASE

Authors

  • Maguinólia Arai
  • Railson Henneberg
  • Aguinaldo José do Nascimento
  • Juliana Yuka Arai
  • Paulo Henrique da Silva

DOI:

https://doi.org/10.5212/publicatio%20uepg.v17i1.3447

Keywords:

Automated reticulocytogram. Sickle cell anemia. Hemoglobin SC. Disease and hemolytic anemia.

Abstract

This work evaluated the erythropoetic behavior of two common hemoglobin SS and SC, using automated reticulocytogram in Sysmex XT 2100, between 1 to 14 years old patients. The group of hemoglobin SS patients showed more intense medullar activity, with higher reticulocytes counting (17% in average) and increase on youngest cell fractions. The SC patients showed high counting in relation to the control group and profile of the reticulocyte fractions congruous of a chronic hemolytic picture, quite different from SS group. The results showed a very characteristic profile in each group and these profiles allowed a laboratory differentiation among the groups. The results are in agreement with other authors, and open perspectives for similar studies, since the knowledge of automated reticulocytogram for the diverse erythrocyte illness is of great clinical importance.

Author Biographies

Maguinólia Arai

Hospital de Clínica da Universidade Federal do Paraná.

Railson Henneberg

Departamento de Patologia Clínica da Universidade Federal do Paraná

Aguinaldo José do Nascimento

Prof. Sênior, Programa de Pós-graduação em Ciências Farmacêuticas, Universidade Federal do Paraná.

Juliana Yuka Arai

Acadêmica do Curso de Medicina da Pontifícia Universidade Católica do Paraná.

Paulo Henrique da Silva

Departamento de Patologia Clínica da Universidade Federal do Paraná