Desmeules Patrice, Joubert Philippe, Zhang Lei, Al-Ahmadie Hikmat A, Fletcher Christopher D, Vakiani Efsevia, Delair Deborah F, Rekhtman Natasha, Ladanyi Marc, Travis William D, Antonescu Cristina R
*Department of Pathology §Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY †Department of Pathology, Quebec Heart and Lung Institute, Quebec, QC, Canada ‡Department of Pathology, Brigham and Women's Hospital, Boston, MA.
Am J Surg Pathol. 2017 Jul;41(7):980-988. doi: 10.1097/PAS.0000000000000864.
Malignant mesothelioma (MM) is a rare, aggressive tumor often associated with asbestos exposure and characterized by complex genetic abnormalities, including deletions of chromosome 22. A gene fusion involving EWSR1 and YY1 gene on 14q32 has been reported in 2 patients over the age of 60 with peritoneal MM. However, the incidence of EWSR1 rearrangements in MM and the spectrum of its fusion partners remain unknown. We recently encountered 2 MM cases with EWSR1-ATF1 fusions and sought to investigate the prevalence and clinicopathologic features associated with this abnormality. As both index cases occurred as intra-abdominal tumors in young adults, we searched our files for pleural and peritoneal MM occurring in adults younger than age of 40. All cases were tested by fluorescence in situ hybridization using custom bacterial artificial chromosomes probes for EWSR1, FUS, and ATF1 genes. When available, immunohistochemistry for BAP1 was performed. A total of 25 MM from patients aged 40 or less were screened, either from peritoneum (n=13) or pleura (n=12), with a median age of 31 (range: 7 to 40 y). Two additional ATF1-rearranged tumors were identified at pleural and peritoneal sites with EWSR1 and FUS as fusion partners, respectively, for a total of 4 cases (16%, 4/25). The fusion-positive cases displayed classic epithelioid morphology, immunoreactivity for cytokeratins and WT1, and negativity for S100. BAP1 expression was retained in the 3 fusion-positive cases with available material, and in 80% (12/15) of the fusion-negative cases. Our results expand the spectrum of tumor types harboring EWSR1/FUS-ATF1 gene fusions to include a subgroup of conventional epithelioid MM. Other features of this unique MM subset include young age at presentation, lack of asbestos exposure and retained BAP1 expression.
恶性间皮瘤(MM)是一种罕见的侵袭性肿瘤,常与石棉暴露相关,其特征为复杂的基因异常,包括22号染色体缺失。在2例60岁以上的腹膜MM患者中,曾报道过涉及14q32上EWSR1和YY1基因的基因融合。然而,MM中EWSR1重排的发生率及其融合伴侣的谱系仍不清楚。我们最近遇到2例伴有EWSR1-ATF1融合的MM病例,并试图研究与这种异常相关的患病率和临床病理特征。由于这2例索引病例均为年轻成人的腹内肿瘤,我们在档案中搜索了40岁以下成人发生的胸膜和腹膜MM病例。所有病例均使用针对EWSR1、FUS和ATF1基因的定制细菌人工染色体探针,通过荧光原位杂交进行检测。如有可能,进行BAP1免疫组化检测。共筛查了40岁及以下患者的25例MM,其中腹膜来源13例,胸膜来源12例,中位年龄为31岁(范围:7至40岁)。在胸膜和腹膜部位分别又鉴定出2例分别以EWSR1和FUS为融合伴侣的ATF1重排肿瘤,共计4例(16%,4/25)。融合阳性病例表现出典型的上皮样形态,细胞角蛋白和WT1免疫反应阳性,S100阴性。在有可用材料的3例融合阳性病例以及80%(12/15)的融合阴性病例中保留了BAP1表达。我们的结果将携带EWSR1/FUS-ATF1基因融合的肿瘤类型谱扩展至包括传统上皮样MM的一个亚组。这个独特的MM亚组的其他特征包括发病年龄较轻、无石棉暴露以及保留BAP1表达。