Successful treatment and integrated genomic analysis of an infant with FIP1L1-RARA fusion–associated myeloid neoplasm

FIP1L1-RARA–a ssociated neoplasm is a very rare and aggressive disease, with only 3 previously reported cases in the literature. Here, we describe a 9-month-old boy who presented with a FIP1L1-RARA fusion–associated myelodysplastic/myeloproliferative neoplasm-like overlap syndrome, with similarities...

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Detalles Bibliográficos
Autores principales: Miltiadous, Oriana, Petrova-Drus, Kseniya, Kaicker, Shipra, Mathew, Susan, Kluk, Michael, Geyer, Julia T., Rodriguez-Sanchez, Irene, Bouvier, Nancy, Inghirami, Giorgio, Stieglitz, Elliot, Khedoudja, Nafa, Benayed, Ryma, Richardson, Michelle, Anderson, Wade, Benhamida, Jamal, You, Daoqi, Londono, Dory, Kung, Andrew L., Prockop, Susan E., Roshal, Mikhail, Zhang, Yanming, Shukla, Neerav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2022
Materias:
Exceptional Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864666/
https://www.ncbi.nlm.nih.gov/pubmed/34551074
http://dx.doi.org/10.1182/bloodadvances.2021004966

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864666/
https://www.ncbi.nlm.nih.gov/pubmed/34551074
http://dx.doi.org/10.1182/bloodadvances.2021004966

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