Co-occurrence of Erdheim-Chester disease and clonally evolving acute myeloid leukemia with FLT3-ITD and PTPN11 mutations
Author:
Funder
Fundamental Research Funds for the Central Universities
Beijing Natural Science Haidian Frontier Foundation
National High Level Hospital Clinical Research Funding
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00277-024-05842-5.pdf
Reference22 articles.
1. Milne P, Bigley V, Bacon CM, Néel A, McGovern N, Bomken S et al (2017) Hematopoietic origin of Langerhans cell histiocytosis and Erdheim-Chester disease in adults. Blood 130(2):167–175
2. Durham BH, Getta B, Dietrich S, Taylor J, Won H, Bogenberger JM et al (2017) Genomic analysis of hairy cell leukemia identifies novel recurrent genetic alterations. Blood 130(14):1644–1648
3. Papo M, Diamond EL, Cohen-Aubart F, Emile JF, Roos-Weil D, Gupta N et al (2017) High prevalence of myeloid neoplasms in adults with non–Langerhans cell histiocytosis. Blood 130(8):1007–1013
4. Goyal G, Liu Y, Ravindran A, Al-Kali A, Go RS, Patnaik MM et al (2019) Concomitant Erdheim-Chester disease and chronic myelomonocytic leukaemia: genomic insights into a common clonal origin. Br J Haematol 187(2):e51–e54
5. Bonnet P, Chasset F, Moguelet P, Abisror N, Itzykson R, Bouaziz JD et al (2019) Erdheim-Chester disease associated with chronic myelomonocytic leukemia harboring the same clonal mutation. Haematologica 104(11):e530–e533
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