Back to Search Start Over

Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia

Authors :
Federica Melazzini
Flavia Palombo
Alessandra Balduini
Daniela De Rocco
Caterina Marconi
Patrizia Noris
Chiara Gnan
Tommaso Pippucci
Valeria Bozzi
Michela Faleschini
Serena Barozzi
Michael Doubek
Christian A. Di Buduo
Katerina Stano Kozubik
Lenka Radova
Giuseppe Loffredo
Sarka Pospisilova
Caterina Alfano
Marco Seri
Carlo L. Balduini
Alessandro Pecci
Anna Savoia
Source :
Haematologica, Vol 101, Iss 11 (2016)
Publication Year :
2016
Publisher :
Ferrata Storti Foundation, 2016.

Abstract

ETV6-related thrombocytopenia is an autosomal dominant thrombocytopenia that has been recently identified in a few families and has been suspected to predispose to hematologic malignancies. To gain further information on this disorder, we searched for ETV6 mutations in the 130 families with inherited thrombocytopenia of unknown origin from our cohort of 274 consecutive pedigrees with familial thrombocytopenia. We identified 20 patients with ETV6-related thrombocytopenia from seven pedigrees. They have five different ETV6 variants, including three novel mutations affecting the highly conserved E26 transformation-specific domain. The relative frequency of ETV6-related thrombocytopenia was 2.6% in the whole case series and 4.6% among the families with known forms of inherited thrombocytopenia. The degree of thrombocytopenia and bleeding tendency of the patients with ETV6-related thrombocytopenia were mild, but four subjects developed B-cell acute lymphoblastic leukemia during childhood, resulting in a significantly higher incidence of this condition compared to that in the general population. Clinical and laboratory findings did not identify any particular defects that could lead to the suspicion of this disorder from the routine diagnostic workup. However, at variance with most inherited thrombocytopenias, platelets were not enlarged. In vitro studies revealed that the maturation of the patients’ megakaryocytes was defective and that the patients have impaired proplatelet formation. Moreover, platelets from patients with ETV6-related thrombocytopenia have reduced ability to spread on fibrinogen. Since the dominant thrombocytopenias due to mutations in RUNX1 and ANKRD26 are also characterized by normal platelet size and predispose to hematologic malignancies, we suggest that screening for ETV6, RUNX1 and ANKRD26 mutations should be performed in all subjects with autosomal dominant thrombocytopenia and normal platelet size.

Details

Language :
English
ISSN :
03906078 and 15928721
Volume :
101
Issue :
11
Database :
Directory of Open Access Journals
Journal :
Haematologica
Publication Type :
Academic Journal
Accession number :
edsdoj.6b19971dee8c490e89c338cc808590ce
Document Type :
article
Full Text :
https://doi.org/10.3324/haematol.2016.147496