Significance of <i>RUNX1</i> mutation in <i>BCR-ABL1</i> positive acute myeloid leukemia – a diagnostic dilemma in a young woman with persistent bleeding-Reference-Cited by-同舟云学术

Significance of RUNX1 mutation in BCR-ABL1 positive acute myeloid leukemia – a diagnostic dilemma in a young woman with persistent bleeding

Published:2022-03-15 Issue:8 Volume:63 Page:1975-1979
ISSN:1042-8194
Container-title:Leukemia & Lymphoma
language:en
Short-container-title:Leukemia & Lymphoma

Author:

Ghosh Sharmila¹,Roth Jacquelyn¹,Babushok Daria²,Lim Megan¹

Affiliation:

1. Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA

2. Blood and Marrow Transplantation Program, Abramson Cancer Center and the Division of Hematology and Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA

Funder

None

Publisher

Informa UK Limited

Subject

Cancer Research,Oncology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10428194.2022.2047673

Reference15 articles.

1. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia

2. AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations

3. A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76.9% of cases

4. Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease

5. Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia

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