Extramedullary haematopoiesis in patients with thalassemia: a cross-sectional description of its prevalence, clinical features and survival.

Extramedullary haematopoiesis Iron Survival T2* magnetic resonance imaging Thalassemia

Journal

Hematology, transfusion and cell therapy
ISSN: 2531-1387
Titre abrégé: Hematol Transfus Cell Ther
Pays: Brazil
ID NLM: 101725732

Informations de publication

Date de publication:
26 Aug 2023
Historique:
received: 29 03 2022
revised: 06 06 2023
accepted: 07 07 2023
medline: 11 9 2023
pubmed: 11 9 2023
entrez: 10 9 2023
Statut: aheadofprint

Résumé

Despite knowledge advances on extramedullary haematopoiesis (EMH) in thalassemic patients, the real picture remains an open issue. To assess EMH prevalence in patients with thalassemia major (TM) and intermedia (TI), to describe magnetic resonance imaging (MRI) findings and to explore clinical risk factors. In this cross-sectional study, images and clinical records of 184 consecutive patients with thalassemia who underwent T2* MRI between 2004 and 2011 were reviewed. Association of EMH with survival was investigated for patients with available follow-up charts. EMH was detected in 16/168 (9.5%) patients with TM (aged 19-49 years) and in 3/16 (18.8%) with TI (aged 36-41 years). Most (88%) had paravertebral thoracic and/or abdominal masses. Age was significantly associated with EMH risk (hazard ratio, [HR] 1.10/year; confidence interval [CI]: 1.03-1.18; p-value < 0.001), while lower pancreatic iron content by T2*MRI (HR: 0.94/ms; CI: 0.89-0.99; p-value = 0.049) was a protective factor. Estimated survival rate was superior for EMH-positive (n = 19) when compared to EMH-negative patients (n = 75) (p-value = 0.013). The prevalence of EMH was 10.3% (19/184), presented mainly as tumoral masses of 3 to 10 cm. Age was a risk factor for EMH development, while lower pancreatic iron might be a protective factor in this cohort.

Identifiants

pubmed: 37690980
pii: S2531-1379(23)00158-X
doi: 10.1016/j.htct.2023.07.005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

Copyright © 2023 Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier España, S.L.U. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest The authors declare no conflicts of interest.

Auteurs

Eduardo Cerello Chapchap (EC)

Hospital Israelita Albert Einstein, São Paulo, SP, Brazil. Electronic address: eduardo.cerello@einstein.br.

Murilo Marques Almeida Silva (MMA)

Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.

Ronaldo Hueb Baroni (RH)

Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.

Aderson da Silva Araujo (ADS)

Fundação de Hematologia e Hemoterapia de Pernambuco (Hemope), Recife, PE, Brazil.

Reijane Alves de Assis (RA)

Fundação de Hematologia e Hemoterapia de Pernambuco (Hemope), Recife, PE, Brazil.

Sandra Regina Loggetto (SR)

Centro de Hematologia de São Paulo, São Paulo, SP, Brazil.

Antonio Fabron Junior (AF)

Hemocentro de Marília, Marília, SP, Brazil.

Monica Pinheiro de Almeida Verissimo (MPA)

Centro Infantil Boldrini, Campinas, SP, Brazil.

Giorgio Roberto Baldanzi (GR)

Centro de Hematologia e Hemoterapia do Paraná - HEMEPAR, Curitiba, PR, Brazil.

Kleber Yotsumoto Fertrin (KY)

Division of Hematology, Department of Medicine, University of Washington, Seattle, WA, USA.

Fernando Tricta (F)

Medical Affairs, ApoPharma, Toronto, CA, Canada.

Antonio Giulio Piga (AG)

Department of Clinical and Biological Sciences, University of Turin, Italy.

Nelson Hamerschlak (N)

Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.

Classifications MeSH