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Burkitt leukemia with precursor B-cell features that developed after ruxolitinib treatment in a patient with hydroxyurea-refractory JAK2(V617F)-myeloproliferative neoplasm

A 62-year-old woman, who had a 16-year history of JAK2(V617F)-mutated myeloproliferative neoplasm (MPN), developed Burkitt leukemia (BL) 16 months after treatment with ruxolitinib to control hydroxyurea-refractory conditions. BL cells were CD10(+), CD19(+), CD20(−), CD34(−), cytoplasmic CD79a(+), an...

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Detalles Bibliográficos
Autores principales: Fukutsuka, Katsuhiro, Iioka, Futoshi, Maekawa, Fumiyo, Nakagawa, Miho, Kishimori, Chiyuki, Hayashida, Masahiko, Tagawa, Shunsuke, Akasaka, Takashi, Honjo, Gen, Ohno, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JSLRT 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265492/
https://www.ncbi.nlm.nih.gov/pubmed/33994432
http://dx.doi.org/10.3960/jslrt.21001
Descripción
Sumario:A 62-year-old woman, who had a 16-year history of JAK2(V617F)-mutated myeloproliferative neoplasm (MPN), developed Burkitt leukemia (BL) 16 months after treatment with ruxolitinib to control hydroxyurea-refractory conditions. BL cells were CD10(+), CD19(+), CD20(−), CD34(−), cytoplasmic CD79a(+), and TdT(+), and lacked surface immunoglobulins but expressed the cytoplasmic μ heavy chain. In the bone marrow, nuclear MYC(+) BL cells displaced the MPN tissues. t(8;14)(q24;q32) occurred at a CG dinucleotide within MYC exon 1 and at the IGHJ3 segment, and an N-like segment was inserted at the junction. The V-D-J sequence of the non-translocated IGH allele had the unmutated configuration. DNA from peripheral blood at a time of the course of MPN exhibited homozygous JAK2(V617F) mutation, while that at BL development included both JAK2(V617F) and wild-type DNAs. Although the association between JAK1/2 inhibitor therapy for MPN and secondary development of aggressive B-cell neoplasm remains controversial, this report suggests that, in selected patients, close monitoring of clonal B-cells in the BM is required before and during treatment with JAK1/2 inhibitors.