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==Chromosomal Rearrangements (Gene Fusions)==
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!Chromosomal Rearrangement!!Genes in Fusion (5’ or 3’ Segments)!!Pathogenic Derivative!!Reference
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|t(5;9)(q33;q22)||''ITK'' / ''SYK''||der(5); der(9)||<ref>{{Cite journal|last=B|first=Streubel|last2=U|first2=Vinatzer|last3=M|first3=Willheim|last4=M|first4=Raderer|last5=A|first5=Chott|date=2006|title=Novel t(5;9)(q33;q22) fuses ITK to SYK in unspecified peripheral T-cell lymphoma|url=https://pubmed.ncbi.nlm.nih.gov/16341044/|language=en|pmid=16341044}}</ref><ref name=":4">{{Cite journal|last=M|first=Wang|last2=S|first2=Zhang|last3=Ss|first3=Chuang|last4=M|first4=Ashton-Key|last5=E|first5=Ochoa|last6=N|first6=Bolli|last7=G|first7=Vassiliou|last8=Z|first8=Gao|last9=Mq|first9=Du|date=2017|title=Angioimmunoblastic T cell lymphoma: novel molecular insights by mutation profiling|url=https://pubmed.ncbi.nlm.nih.gov/28148900/|language=en|doi=10.18632/oncotarget.14846|pmc=PMC5392284|pmid=28148900}}</ref>
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|t(7;14)(q35;q32.1)
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|''TRB/TCL1A''
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|der(7); der(14)
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|<ref>{{Cite journal|last=Mf|first=Cosimi|last2=I|first2=Casagranda|last3=G|first3=Ghiazza|last4=G|first4=Rossi|last5=P|first5=Galvani|date=1990|title=Rearrangements on chromosomes 7 and 14 with breakpoints at 7q35 and 14q11 in angioimmunoblastic lymphadenopathy and IBL-like T-cell lymphoma|url=https://pubmed.ncbi.nlm.nih.gov/2284141/|language=en|pmid=2284141}}</ref>
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|t(14;14)(q11;q32.1) / inv(14)(q11q32.1)
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|''TRA-TRD/TCL1A''
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|der(14)
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|<ref>{{Cite journal|last=B|first=Schlegelberger|last2=A|first2=Feller|last3=A|first3=Himmler|last4=W|first4=Grote|date=1990|title=Inv(14)(q11q32) in one of four different clones in a case of angioimmunoblastic lymphadenopathy|url=https://pubmed.ncbi.nlm.nih.gov/2293883/|language=en|pmid=2293883}}</ref><ref>{{Cite journal|last=E|first=Leich|last2=E|first2=Haralambieva|last3=A|first3=Zettl|last4=A|first4=Chott|last5=T|first5=Rüdiger|last6=S|first6=Höller|last7=Hk|first7=Müller-Hermelink|last8=G|first8=Ott|last9=A|first9=Rosenwald|date=2007|title=Tissue microarray-based screening for chromosomal breakpoints affecting the T-cell receptor gene loci in mature T-cell lymphomas|url=https://pubmed.ncbi.nlm.nih.gov/17582237/|language=en|pmid=17582237}}</ref>
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|chr(2)(q33.2)
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|''CTLA4/CD28''
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|der(2)
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|<ref>{{Cite journal|last=Hy|first=Yoo|last2=P|first2=Kim|last3=Ws|first3=Kim|last4=Sh|first4=Lee|last5=S|first5=Kim|last6=Sy|first6=Kang|last7=Hy|first7=Jang|last8=Je|first8=Lee|last9=J|first9=Kim|date=2016|title=Frequent CTLA4-CD28 gene fusion in diverse types of T-cell lymphoma|url=https://pubmed.ncbi.nlm.nih.gov/26819049/|language=en|doi=10.3324/haematol.2015.139253|pmc=PMC5013939|pmid=26819049}}</ref>
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==Characteristic Chromosomal Aberrations / Patterns==
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*Clonal rearrangement in T-Cell receptor gene in 75-90% of AITL cases<ref name=":7">{{Cite journal|last=Ad|first=Attygalle|last2=Ss|first2=Chuang|last3=Tc|first3=Diss|last4=Mq|first4=Du|last5=Pg|first5=Isaacson|last6=A|first6=Dogan|date=2007|title=Distinguishing angioimmunoblastic T-cell lymphoma from peripheral T-cell lymphoma, unspecified, using morphology, immunophenotype and molecular genetics|url=https://pubmed.ncbi.nlm.nih.gov/17448026/|language=en|pmid=17448026}}</ref> <ref>{{Cite journal|last=L|first=de Leval|last2=C|first2=Gisselbrecht|last3=P|first3=Gaulard|date=2010|title=Advances in the understanding and management of angioimmunoblastic T-cell lymphoma|url=https://pubmed.ncbi.nlm.nih.gov/19961485/|language=en|pmid=19961485}}</ref><ref name=":8">{{Cite journal|last=Bt|first=Tan|last2=Ra|first2=Warnke|last3=Da|first3=Arber|date=2006|title=The frequency of B- and T-cell gene rearrangements and epstein-barr virus in T-cell lymphomas: a comparison between angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma, unspecified with and without associated B-cell proliferations|url=https://pubmed.ncbi.nlm.nih.gov/16931587/|language=en|doi=10.2353/jmoldx.2006.060016|pmc=PMC1867616|pmid=16931587}}</ref>
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*Clonal rearrangement in immunoglobulin genes in 25-30% of AITL cases<ref name=":7" /><ref name=":8" />
      
==Genomic Gain/Loss/LOH==
 
==Genomic Gain/Loss/LOH==
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==Epigenomics (Methylation)==
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*Frequent mutation in epigenetic modifiers like: <ref name=":4" /><ref name=":5" /><ref name=":11" /><ref name=":12" />
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**''IDH2'' (20-30%)
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**''TET2'' (50-80%)
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**''DNMT3A'' (20-30%)
      
==Diagnostic Testing Methods==
 
==Diagnostic Testing Methods==