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作 者:Laila M Sherief Esmael Goneim Naglaa M Kamal Amr Ibraheim Fuad Alsofiani Abdulraouf Alawur
机构地区:[1]Department of Pediatric Hematology and Oncology,Faculty of Medicine,Zagazig University,Zagazig 44511,Egypt [2]Department of Pediatrics,Faculty of Medicine,Zagazig University,Zagazig 44511,Egypt [3]Department of Pediatric Oncology,Tanta Cancer Institute,Tanta 00202,Egypt [4]Department of Pediatrics and Pediatric Hepatology,Faculty of Medicine,Cairo University,Cairo 21121,Egypt [5]Fuad A alsofiani,Abdulraouf H Alawur,Department of Pediatrics,Alhada Armed Forces Hospital,Taif 00966,Saudi Arabia
出 处:《World Journal of Clinical Pediatrics》2020年第1期1-6,共6页世界临床儿科杂志
摘 要:BACKGROUNDβ-thalassemia intermedia(βTI)is one of the hemoglobinopathies.It constitutes 10%ofβ-thalassemia cases yet being associated with a better quality of life thanβ-thalassemia major(βTM).CASE SUMMARY We recently reported the first case of acute lymphoblastic leukemia(ALL)from Egypt in a child withβTM,and we herein report the first case of ALL from Egypt in a child withβTI.In this report,literature was reviewed for cases of malignancies associated withβTI and the possible factors underling the relationship between the two entities.CONCLUSION We stress that physicians should have a high index of suspicion of malignancies in thalassemia patients if they present with any suggestive symptoms or signs.
关 键 词:Acute lymphoblastic leukemia Thalassemia intermedia Children MALIGNANCIES Iron overload HYDROXYUREA Case report
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