100% HbF Found Thalassemia Intermedia Case in Peripheral Blood Periferik Kanında %100 HbF Bulunan Talasemi İntermedia Olgusu


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Kurtoğlu A. U., Uçar H., Eren E., Aslan V., KURTOĞLU E., Yılmaz N.

Genel Tip Dergisi, cilt.31, sa.2, ss.180-181, 2021 (Scopus, TRDizin)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 31 Sayı: 2
  • Basım Tarihi: 2021
  • Doi Numarası: 10.15321/geneltipder.2021.310
  • Dergi Adı: Genel Tip Dergisi
  • Derginin Tarandığı İndeksler: Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.180-181
  • Anahtar Kelimeler: Beta globin gene deletion, HbF, Thalassemia Intermedia
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Sağlık Bilimleri Üniversitesi Adresli: Evet

Özet

Hb F is synthesized in the gestational period and the amount decreases gradually with delivery. In an adult person, Hb F is <2%. The affinity of HbF to oxygen is higher than HbA. HbF is therefore not suitable for transporting oxygen to tissues. In this study; We investigated the hematological and biochemical changes in an adult patient with 100% HbF in peripheral blood. Complete blood count of a 66-year-old male patient followed up in hematology clinic with symptoms of anemia; RBC: 3.1 1012 / L, Hb: 8.3 g / dL, Hct: 27.6%, MCV: 90.1 f / L, PLT: 793 000 103 / mm3. Serum ferritin: 1094 ng / mL, total bilirubin: 4 mg / dL, direct bilirubin: 0.68 mg / dL. The hemoglobin variant analysis revealed 100% HbF. The patient had no HbA. The patient was evaluated as thalassemia intermedia.