Fatma Gümrük

İbrahim Kulaç

Şule Ünal

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45 Images in HematologyBrilliant cresyl blue staining for screening hemoglobin H disease: Reticulocyte smearHemoglobin H hastalığında görüntüleme için brilliant cresyl blue boyaması: Retikülosit yaymasıİbrahim Kulaç1, Şule Ünal2, Fatma Gümrük21Hacettepe University, Faculty of Medicine, Ankara, Turkey2Division of Pediatric Hematology, Hacettepe University, Faculty of Medicine, Ankara, TurkeyAddress for Correspondence: Dr. Şule Ünal, Hacettepe University, Division of Pediatric Hematology 06100 Ankara, Turkey Phone: +90 312 305 11 70 E-mail: suleunal@hacettepe.edu.trA three-year-old boy was referred to our hospital with the complaint of anemia resistant to iron treatment. Laboratory examination revealed hemoglobin (Hb): 8.7 g/dl, hematocrit (Hct): 30%, red blood cell (RBC): 5.5x109/L, mean corpuscular volume (MCV): 54 fL, red cell distribution width (RDW): 21.6%, and platelet: 448x109/L. Peripheral blood smear examination revealed hypochromia, microcytosis, poikilocytosis and anisocy-tosis. Reticulocyte count was 1%. The personal history was unremarkable and there was no consanguinity between parents. He had received no transfusions. Physical examination was unremarkable except for mild pallor and mild splenomegaly. Serum iron concentration and serum total iron binding capacity were 77 μmol/L and 362 μmol/L, respectively, and the transferrin saturation was 21.2%. Hemoglobin electrophoresis revealed HbA2: 1.5%, HbF: 1.9%, and HbH: 3.6%. We observed numer-ous RBCs containing hemoglobin H (HbH) inclusions in the peripheral blood smear stained with brilliant cresyl blue (Figure1). Beta Globin Strip Assay (Vienna Lab; Vienna, Austria) was based on reverse hybridization. The mutational analyses using alpha Globin Strip Assay (Vienna Lab; Vienna, Austria) of the family revealed that the patient had - - MED II(-26.5)/-α3.7 deletions; the mother and father were found to have - - MED II(-26.5) and -α3.7 deletions, respectively.Although HbH is a common disease, it is rarely reported because of low suspicion [1,2]. In patients with hypochromic microcytic anemia without β-thalassemia trait and iron defi-ciency, a simple reticulocyte stain can serve as a useful early rapid screening tool for detecting inclusions in patients with HbH disease.This staining can be used as a screening procedure where the molecular diagnosis of HbH disease is not possible.References 1.  Papassotiriou I, Traeger-Synodinos J, Kanavakis E, Karagiorga M, Stamoulakatou A, Kattamis C. Erythroid marrow activity and hemo-globin H levels in hemoglobin H disease. J Pediatr Hematol Oncol. 1998;20:539-544. 2.  Chan LC, So JC, Chui DH. Comparison of haemoglobin H inclu-sion bodies with embryonic zeta globin in screening for alpha thalassaemia. J Clin Pathol. 1995;48:861-864.Figure 1. Erythrocytes containing HbH inclusions in brilliant cresyl blue-stained smear

Brilliant cresyl blue staining for screening hemoglobin H disease: Reticulocyte smear

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