A Case of 8p11 Myeloproliferative Syndrome withBCR-FGFR1Gene Fusion Presenting with Trilineage Acute Leukemia/Lymphoma, Successfully Treated by Cord Blood Transplantation-Reference-Cited by-同舟云学术

A Case of 8p11 Myeloproliferative Syndrome withBCR-FGFR1Gene Fusion Presenting with Trilineage Acute Leukemia/Lymphoma, Successfully Treated by Cord Blood Transplantation

Published:2013 Issue:2 Volume:129 Page:83-89
ISSN:1421-9662
Container-title:Acta Haematologica
language:en
Short-container-title:Acta Haematol

Author:

Morishige Satoshi,Oku Eijiro,Takata Yuka,Kimura Yoshizo,Arakawa Fumiko,Seki Ritsuko,Imamura Rie,Osaki Koichi,Hashiguchi Michitoshi,Yakushiji Kazuaki,Mizuno Shinichi,Yoshimoto Koji,Nagafuji Koji,Ohshima Koichi,Okamura Takashi

Publisher

S. Karger AG

Subject

Hematology,General Medicine

Reference30 articles.

1. A syndrome of lymphoblastic lymphoma, eosinophilia, and myeloid hyperplasia/malignancy associated with t(8;13)(p11;q11): description of a distinctive clinicopathologic entity [see comments]

2. Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1

3. t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12

4. FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome

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2. Myeloid/lymphoid neoplasms with eosinophilia and tyrosine kinase gene fusions: reevaluation of the defining characteristics in a registry-based cohort;Leukemia;2023-07-15

3. Rare case of pediatric trilineal mixed-phenotype acute leukemia with t(11;19)(q23.3;p13)/KMT2A::ELL;Leukemia Research;2023-02

4. The 8p11 myeloproliferative syndrome: Genotypic and phenotypic classification and targeted therapy;Frontiers in Oncology;2022-11-03

5. Identification of a novel HOOK3-FGFR1 fusion gene involved in activation of the NF-kappaB pathway;Cancer Cell International;2022-01-26