关键词: ALK‐negative CD15 CD30 anaplastic large cell lymphoma peripheral T‐cell lymphoma

Mesh : Female Humans Male Anaplastic Lymphoma Kinase / genetics metabolism Dual-Specificity Phosphatases / genetics Gene Rearrangement Interferon Regulatory Factors / genetics metabolism Ki-1 Antigen / metabolism genetics analysis Lewis X Antigen / analysis metabolism Lymphoma, Large-Cell, Anaplastic / genetics pathology diagnosis Lymphoma, T-Cell, Peripheral / genetics metabolism pathology diagnosis Mitogen-Activated Protein Kinase Phosphatases / genetics

来  源:   DOI:10.1111/bjh.19442

Abstract:
Peripheral T-cell lymphomas (PTCL) are morphologically and biologically heterogeneous and a subset expresses CD30, including anaplastic large cell lymphomas (ALCL) and a minority of PTCL, not otherwise specified (PTCL, NOS). ALCL with ALK translocations (ALCL, ALK+) are readily identified by routine diagnostic methods, but differentiating ALCL without ALK translocation (ALCL, ALK-) and PTCL, NOS expressing CD30 (PTCL CD30+) can be challenging. Furthermore, rare PTCL co-express CD30 and CD15 (PTCL CD30+CD15+); some resemble ALCL, ALK- while others resemble classic Hodgkin lymphoma. To explore the relationship between PTCL CD30+CD15+ and ALCL, ALK-, we analysed 19 cases of PTCL with CD30 expression, previously diagnosed as ALCL, ALK- (nine cases) and PTCL CD30+CD15+ (10 cases) for DUSP22/IRF4 rearrangements, coding RNA expression and selected transcriptome analysis using the NanoString nCounter gene expression analysis platform. Unsupervised clustering showed no clear segregation between ALCL, ALK- and PTCL CD30+CD15+. Three cases previously classified as PTCL CD30+CD15+ showed DUSP22/IRF4 rearrangements, favouring a diagnosis of ALCL, ALK-. Our results suggest that cases previously designated PTCL CD30+CD15+, likely fall within the spectrum of ALCL, ALK-; additionally, a subset of ALCL, ALK- with DUSP22/IRF4 rearrangement expresses CD15, consistent with previous reports and expands the immunophenotypic spectrum of this lymphoma subgroup.
摘要:
外周T细胞淋巴瘤(PTCL)在形态和生物学上是异质的,并且一个子集表达CD30,包括间变性大细胞淋巴瘤(ALCL)和少数PTCL,未指定(PTCL,NOS).具有ALK易位的ALCL(ALCL,ALK+)很容易通过常规诊断方法识别,但区分无ALK易位的ALCL(ALCL,ALK-)和PTCL,NOS表达CD30(PTCLCD30+)可能是具有挑战性的。此外,罕见的PTCL共表达CD30和CD15(PTCLCD30+CD15+);有些类似ALCL,ALK-而其他类似于经典的霍奇金淋巴瘤。探讨PTCLCD30+CD15+与ALCL的关系,ALK-,我们分析了19例CD30表达的PTCL,以前诊断为ALCL,ALK-(9例)和PTCLCD30+CD15+(10例)用于DUSP22/IRF4重排,编码RNA表达和使用NanoStringnCounter基因表达分析平台选择的转录组分析。无监督聚类显示ALCL之间没有明显的隔离,ALK-和PTCLCD30+CD15+。先前分类为PTCLCD30+CD15+的3例显示DUSP22/IRF4重排,有利于ALCL的诊断,ALK-。我们的结果表明,以前指定为PTCLCD30+CD15+的病例,可能属于ALCL的范围,ALK-;另外,ALCL的一个子集,具有DUSP22/IRF4重排的ALK-表达CD15,与以前的报道一致,并扩展了该淋巴瘤亚组的免疫表型谱。
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