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Acute lymphoblastic leukemia in a β-thalassemia intermedia child: A case report

BACKGROUND: β-thalassemia intermedia (βTI) is one of the hemoglobinopathies. It constitutes 10% of β-thalassemia cases yet being associated with a better quality of life than β-thalassemia major (βTM). CASE SUMMARY: We recently reported the first case of acute lymphoblastic leukemia (ALL) from Egypt...

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Detalles Bibliográficos
Autores principales: Sherief, Laila M, Goneim, Esmael, Kamal, Naglaa M, Ibraheim, Amr, Alsofiani, Fuad, Alawur, Abdulraouf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416358/
https://www.ncbi.nlm.nih.gov/pubmed/32844089
http://dx.doi.org/10.5409/wjcp.v9.i1.1
Descripción
Sumario:BACKGROUND: β-thalassemia intermedia (βTI) is one of the hemoglobinopathies. It constitutes 10% of β-thalassemia cases yet being associated with a better quality of life than β-thalassemia major (βTM). CASE SUMMARY: We recently reported the first case of acute lymphoblastic leukemia (ALL) from Egypt in a child with βTM, and we herein report the first case of ALL from Egypt in a child with βTI. In this report, literature was reviewed for cases of malignancies associated with βTI 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.