Thalassemia and malignancy: An emerging concern?
Cancer
Iron overload
Malignancies
Thalassemia
Transfusion
Journal
Blood reviews
ISSN: 1532-1681
Titre abrégé: Blood Rev
Pays: England
ID NLM: 8708558
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
18
02
2019
revised:
05
05
2019
accepted:
20
06
2019
pubmed:
30
6
2019
medline:
25
1
2020
entrez:
30
6
2019
Statut:
ppublish
Résumé
The thalassemias constitute a variable group of anemias that result from autosomal recessive inherited defects in the production of hemoglobin. The life expectancy of thalassemia patients has been extended over the last decades as a result of key milestones being achieved in optimizing management with transfusion and iron chelation therapy. Such advances have prolonged the survival of thalassemia patients and improved their overall quality of life. However, this increase in life expectancy has led to the manifestation of several morbidities, including multiple types of solid and hematologic malignancies. In this review we report the different types of solid and hematological malignancies that can develop in thalassemia patients, in addition to the possible predisposing factors and mechanisms behind their development.
Identifiants
pubmed: 31253373
pii: S0268-960X(19)30016-5
doi: 10.1016/j.blre.2019.06.002
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
100585Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.