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CSF3R T618I mutated chronic myelomonocytic leukemia: A proliferative subtype with a distinct mutational profile.
Kwon, Adelaide; Ibrahim, Ibrahim; Le, Tri; Jaso, Jesse Manuel; Weinberg, Olga; Fuda, Franklin; Chen, Weina.
Afiliação
  • Kwon A; Medical School, University of Texas Southwestern Medical Center at Dallas, TX, USA.
  • Ibrahim I; Departments of Internal Medicine/Division of Hematology and Oncology, University of Texas Southwestern Medical Center at Dallas, TX, USA.
  • Le T; Departments of Internal Medicine/Division of Hematology and Oncology, University of Texas Southwestern Medical Center at Dallas, TX, USA.
  • Jaso JM; Department of Pathology, University of Texas Southwestern Medical Center at Dallas, 2330 Inwood Rd, TX, 75390-9317 USA.
  • Weinberg O; Department of Pathology, University of Texas Southwestern Medical Center at Dallas, 2330 Inwood Rd, TX, 75390-9317 USA.
  • Fuda F; Department of Pathology, University of Texas Southwestern Medical Center at Dallas, 2330 Inwood Rd, TX, 75390-9317 USA.
  • Chen W; Department of Pathology, University of Texas Southwestern Medical Center at Dallas, 2330 Inwood Rd, TX, 75390-9317 USA.
Leuk Res Rep ; 17: 100323, 2022.
Article em En | MEDLINE | ID: mdl-35586707
ABSTRACT
Chronic myelomonocytic leukemia (CMML) is a clonal myeloid neoplasm characterized by sustained monocytosis and mutations in TET2, ASXL1, SRSF2, SETBP1, NRAS, and KRAS. We describe a rare case of CSF3R T618I mutated CMML that has a proliferative phenotype, myelodysplasia, and additional mutations in ASXL1, SETBP1, KRAS, and PTPN11. Comparing the clinicopathologic features of this case to previously reported cases of CSF3R T618I mutated CMML and CSF3R non-T618I mutated CMML, CSF3R T618I seems to define a unique proliferative subtype of CMML with a distinct mutational profile. The diagnostic challenges and molecular pathogenesis associated with this case are also briefly discussed.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article