| Literature DB >> 32815876 |
Astrid Behnert1,2, Alex G Lee1,2, Elizabeth P Young1, Marcus R Breese1,2, Stanley G Leung1,2, Inge Behroozfard1, Maria Maruffi3, E Alejandro Sweet-Cordero1,2, Christopher C Dvorak1,2, Julia Chu1, Elliot Stieglitz1,2.
Abstract
Overlapping myelodysplastic/myeloproliferative neoplasms (MDS/MPN) are clonal hematopoietic disorders with features of myelodysplasia and myeloproliferation. The only well-characterized MDS/MPN in children is juvenile myelomonocytic leukemia, an aggressive disorder of infants and toddlers. The biochemical hallmark of this disease is hyperactivation of the Ras/MAPK signaling pathway caused by mutations in Ras pathway genes in more than 90% of patients. Translocations involving receptor tyrosine kinases have been identified in rare cases. Here, we report a 2-year-old patient who presented with MDS/MPN driven by a cytogenetically cryptic NUP98-NSD1 fusion, a translocation thought to exclusively occur in patients with acute myeloid leukemia.Entities:
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Year: 2021 PMID: 32815876 PMCID: PMC7889745 DOI: 10.1097/MPH.0000000000001913
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.170