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TFG::ALK fusion in ALK positive large B-cell lymphoma: a case report and review of literature
被引:1
|作者:
Xiao, Andrew
[1
]
Shahmarvand, Nahid
[2
]
Nagy, Alexandra
[1
]
Kumar, Jyoti
[3
,4
]
Van Ziffle, Jessica
[1
]
Devine, Patrick
[1
]
Huang, Franklin
[1
]
Lezama, Lhara
[5
]
Li, Peng
[6
,7
]
Ohgami, Robert S. S.
[1
,6
,7
]
机构:
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94115 USA
[2] Syneos Hlth, Morrisville, NC USA
[3] Stanford Univ, Dept Pathol, Stanford, CA USA
[4] Mem Sloan Kettering Canc Ctr, Dept Pathol & Lab Med, New York, NY USA
[5] Kaiser Permanente, Dept Pathol, Los Angeles, CA USA
[6] Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USA
[7] ARUP Labs, Salt Lake City, UT 84108 USA
来源:
FRONTIERS IN ONCOLOGY
|
2023年
/
13卷
关键词:
ALK plus large B-cell lymphoma;
TFG;
ALK;
ALK translocation;
ALK fusion;
INFLAMMATORY MYOFIBROBLASTIC TUMORS;
GENE;
VARIANT;
KINASE;
TRANSLOCATIONS;
IDENTIFICATION;
THERAPY;
D O I:
10.3389/fonc.2023.1174606
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Anaplastic lymphoma kinase (ALK) positive large B-cell lymphoma (ALK+ LBCL) is an aggressive and rare subtype of B-cell lymphoma. Patients typically present with advanced clinical stage disease and do not respond to conventional chemotherapy; the median overall survival is 1.8 years. The genetic landscape of this entity remains poorly understood. Here we report a unique case of ALK+ LBCL harbouring a rare TFG::ALK fusion. Targeted next-generation sequencing showed no significant single nucleotide variants, insertions/deletions, or other structural variants beyond the TFG::ALK fusion; deep deletions of FOXO1, PRKCA, and the MYB locus were also detected. Our case report draws attention to this rare disease, highlights a need for larger genetic profiling studies, and focuses on the pathogenesis and potential therapeutic targets of this aggressive disease. To our knowledge, this is the first report of a TFG::ALK fusion in ALK+ LBCL.
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