Issaragrisil S
Department of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Blood Cells. 1994;20(2-3):259-62; discussion 263.
Thalassemias and hemoglobinopathies are prevalent in Thailand. Bone marrow transplantation can cure thalassemia, but less than 30% of the patients have an HLA-identical sibling. Cord blood is an alternative source of stem cells for transplantation. By prenatal diagnosis, the fetus can be diagnosed as having thalassemic disease. DNA typing for HLA will be performed. Cord blood can be collected for transplantation if the fetus is not affected and is HLA-identical to the patient. We report a successful cord blood transplantation in a patient with beta-thalassemia/hemoglobin E disease.
地中海贫血和血红蛋白病在泰国很常见。骨髓移植可以治愈地中海贫血,但只有不到30%的患者有人类白细胞抗原(HLA)匹配的同胞。脐血是移植干细胞的另一种来源。通过产前诊断,可以诊断出胎儿患有地中海贫血疾病。将进行HLA的DNA分型。如果胎儿未受影响且与患者HLA匹配,则可以采集脐血用于移植。我们报告了一例成功的脐血移植治疗β地中海贫血/血红蛋白E病患者的病例。