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Extramedullary hematopoiesis (EMH) results from the extension of hematopoietic tissue beyond the confines of the bones. Since the initiation of regular transfusion programs from an early age for all thalassemia major (ΤΜ) patients, EMH has not been considered a clinical issue anymore. The present study aims to record the prevalence of EMH in chronically transfused ΤΜ patients followed at our institution and to investigate possible risk factors associated with its occurrence. The project was designed as a retrospective, nonexperimental, descriptive, exploratory study. In total, the study enrolled 104 patients. EMH was revealed in 15/104 (14%) patients. The presence of intravening sequence (IVS)-I-6 was significantly related with the development of EMH (p < 0.05). No other demographic or biological factor studied was found to be related with the presence of EMH. The study stresses a profound incidence of asymptomatic EMH in a solid group of well-transfused ΤΜ patients. Given the high incidence of the IVS-I-6 allele in the Mediterranean and Middle Eastern region, high-quality, prospective, multicenter studies could confirm the association of EMH occurrence with the presence of the IVS-I-6 mutation and further evaluate the exact role of this mutation in the EMH process.

Original publication

DOI

10.1159/000463919

Type

Journal article

Journal

Acta Haematol

Publication Date

2017

Volume

137

Pages

175 - 182

Keywords

Extramedullary hematopoiesis, IVS-I-6 genotype, Thalassemia major, Adult, Alleles, Female, Genotype, Greece, Hematopoiesis, Extramedullary, Humans, Incidence, Male, Middle Aged, Mutation, Retrospective Studies, Risk Factors, Young Adult, beta-Globins, beta-Thalassemia