A novel bi-alleleic DDX41 mutations in B-cell lymphoblastic leukemia: case report

Woo Yong Shin(Soonchunhyang University Hospital Seoul), Seug Yun Yoon(Soonchunhyang University Hospital Seoul), Rojin Park(Soonchunhyang University Hospital Seoul), Jung‐Ah Kim(Soonchunhyang University Hospital Seoul), Ho Hyun Song(Soonchunhyang University), Hae In Bang(Soonchunhyang University Hospital Seoul), Jong-Ho Won(Soonchunhyang University Hospital Seoul), Jieun Kim(Soonchunhyang University Hospital Seoul)
BMC Medical Genomics
March 4, 2022
Cited by 9Open Access
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Abstract

BACKGROUND: The germline mutations of DDX41, also known as DEAD box RNA helicase 41, have been found in about 1.5% of myeloid neoplasms (MNs). Development of MDS/AML is relatively common in germline DDX41 mutations. However, a variety of hematological malignancies (HMs) have been reported. CASE PRESENTATION: We report a novel case of bi-alleleic DDX41 mutations in B-cell lymphoblastic leukemia (B-ALL), with unusual location of DDX41 mutations. The gene expression profile (GEP) of Ph + B-ALL with bi-alleleic DDX41 mutations showed heterogeneously transitional GEP and altered gene expression levels of genes involved in the process essential for red blood cells and myeloid cell differentiation were noted. CONCLUSIONS: We report that DDX41 mutations are unusual but can be an underlying event in Ph + B-ALL and screening DDX41 mutations can be also informative for patients awaiting for haploidentical stem cell transplantation and choosing the therapy.


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