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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页数:6
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