Reclassification of diffuse large B cell lymphoma to large B cell lymphoma with IRF4 rearrangement in an adult population

被引:4
|
作者
Hesius, Eva A. M. [1 ]
van Laar, Lidia [2 ,3 ]
Oosterveld, Margriet [4 ]
van Spriel, Annemiek B. [5 ]
Scheijen, Blanca [6 ]
Leeuwis, Jan Willem [2 ]
Marres, Henri A. M. [7 ]
Groenen, Patricia J. T. A. [6 ]
Stevens, Wendy B. C. [1 ]
van Der Spek, Ellen [8 ]
van den Brule, Adriaan J. C. [9 ]
Hoevenaars, Brigiet M. [10 ]
Hebeda, Konnie M. [6 ]
van den Brand, Michiel [2 ,6 ]
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Hematol, Nijmegen, Netherlands
[2] Rijnstate Hosp, Pathol DNA, Arnhem, Netherlands
[3] St Antonius Hosp, Pathol DNA, Nieuwegein, Netherlands
[4] Canisius Wilhelmina Hosp, Dept Hematol, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen Med Ctr, Radboud Inst Mol Life Sci, Dept Tumor Immunol, Nijmegen, Netherlands
[6] Radboud Univ Nijmegen Med Ctr, Dept Pathol, POB 9101, NL-6500 HB Nijmegen, Netherlands
[7] Radboud Univ Nijmegen Med Ctr, Dept Otorhinolaryngol & Head & Neck Surg, Nijmegen, Netherlands
[8] Rijnstate Hosp, Dept Hematol, Arnhem, Netherlands
[9] Jeroen Bosch Hosp, Pathol DNA, Den Bosch, Netherlands
[10] Canisius Wilhelmina Hosp, Dept Pathol, Nijmegen, Netherlands
基金
欧洲研究理事会;
关键词
diffuse large B cell lymphoma; IRF4; translocation; large B cell lymphoma; CHILDREN;
D O I
10.1111/his.14885
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
AimsLarge B cell lymphoma with IRF4 rearrangement (LBCL-IRF4) is a new entity in the 2017 revised World Health Organisation (WHO) classification that was initially mainly reported in children. After identification of a 79-year-old patient, we assessed how often IRF4 rearrangements can be detected in adult diffuse large B cell lymphomas (DLBCLs) which have to be reclassified to LBCL-IRF4 based on fluorescence in-situ hybridisation (FISH) for IRF4. Methods and resultsWith FISH, we studied the presence of IRF4 rearrangements in 238 lymphomas that were diagnosed as DLBCL according to the previous WHO classification of 2008. ConclusionsIn addition to the index patient, an IRF4 rearrangement was detected in another five of 237 patients (2%). The immunohistochemical profile of these five IRF4 rearranged lymphomas was consistent with previous reports of LBCL-IRF4. One case was recognised to represent transformation of follicular lymphoma rather than de-novo LBCL-IRF4. BCL6 rearrangements were found in two cases of LBCL-IRF4; BCL2 and MYC rearrangements were excluded. Patients presented with limited stage disease with involvement of the head and neck in three patients, and involvement of the lung and thyroid in two others. This study shows that, although rare, LBCL-IRF4 should also be considered in older patients and at localisations other than the head and neck region.
引用
收藏
页码:1013 / 1020
页数:8
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