Malignant Mesothelioma With EWSR1-ATF1 Fusion in Two Adolescent Male Patients.

IF 1.3
Hezhen Ren, S Rod Rassekh, Atilano Lacson, Cheng-Han Lee, Brendan C Dickson, Catherine T Chung, Anna F Lee
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引用次数: 11

Abstract

Malignant mesothelioma is a neoplasm of serosal surfaces, most commonly affecting the pleura. The peritoneum, pericardium, and tunica vaginalis are less frequently involved. Malignant mesothelioma with EWSR1-ATF1 fusion in young adults was recently reported in the literature. Here, we present two pediatric cases of EWSR1-ATF1 translocation-associated malignant mesothelioma in the peritoneum and pericardium respectively. Both cases lacked a known exposure history. Microscopy in both cases showed predominantly epithelioid morphology with ample eosinophilic cytoplasm, and immunohistochemistry was positive for pan-keratin, calretinin, and WT1. Both cases showed EWSR1-ATF1 gene rearrangement by RNA sequencing, which was instrumental in confirming the diagnosis of malignant mesothelioma and to exclude more common pediatric sarcomas, especially in the context of limited sampling.

Abstract Image

Abstract Image

2例青少年男性恶性间皮瘤伴EWSR1-ATF1融合。
恶性间皮瘤是一种浆膜表面的肿瘤,最常累及胸膜。腹膜、心包和阴道膜较少受累。恶性间皮瘤合并EWSR1-ATF1融合在年轻人最近的文献报道。在此,我们报告两例分别发生在腹膜和心包膜的EWSR1-ATF1易位相关的儿童恶性间皮瘤。两例均无已知暴露史。显微镜下两例均显示上皮样形态为主,嗜酸性细胞质丰富,免疫组化pan-keratin, calretinin和WT1阳性。通过RNA测序,这两例病例均显示EWSR1-ATF1基因重排,这有助于确认恶性间皮瘤的诊断,并排除更常见的儿童肉瘤,特别是在样本有限的情况下。
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