5岁男孩面部EWSR1-PATZ1融合的圆细胞肉瘤:一个异常组织学特征的病例报告。

Head and neck pathology Pub Date : 2021-12-01 Epub Date: 2021-01-18 DOI:10.1007/s12105-021-01285-w
Derek Tsz Wai Yau, Shun Wong, Chit Chow, Ka Fai To
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引用次数: 4

摘要

EWSR1-PATZ1融合的圆形细胞肉瘤是罕见的多表型肉瘤,在免疫组织化学上通常表现为神经和肌源性分化。组织学特征为由相对单调的梭形细胞组成的小叶状细胞束和被纤维化基质隔开的蓝色小圆细胞。目前,EWSR1-PATZ1肉瘤的临床行为尚不确定,即使在转移病例中也报道了不同的结果。我们在此报告另一例5岁男孩面部EWSR1-PATZ1融合相关的圆细胞肉瘤,其异常的组织学特征为苍白带,玫瑰花结/腺样结构和上皮标志物的表达。使用EWSR1分离探针进行荧光原位杂交研究(FISH)结果为阴性,需要进行RNA测序的分子研究来确诊。这些发现突出了FISH研究在EWSR1-PATZ1肉瘤中的诊断挑战和潜在缺陷。需要进一步的研究来增加对它们的行为,形态谱和分子特征的理解,这将有助于制定新的治疗策略来治疗这些罕见的肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Round Cell Sarcoma with EWSR1-PATZ1 Fusion in the Face of a Five-Year-Old Boy: Report of a Case with Unusual Histologic Features.

Round Cell Sarcoma with EWSR1-PATZ1 Fusion in the Face of a Five-Year-Old Boy: Report of a Case with Unusual Histologic Features.

Round Cell Sarcoma with EWSR1-PATZ1 Fusion in the Face of a Five-Year-Old Boy: Report of a Case with Unusual Histologic Features.

Round Cell Sarcoma with EWSR1-PATZ1 Fusion in the Face of a Five-Year-Old Boy: Report of a Case with Unusual Histologic Features.

Round cell sarcomas with EWSR1-PATZ1 fusion are rare polyphenotypic sarcomas that typically show both neural and myogenic differentiation on immunohistochemistry. The histology features lobular admixture of cellular fascicles of relatively monotonous spindle cells and small blue round cells separated by fibrotic stroma. The clinical behavior of EWSR1-PATZ1 sarcoma is uncertain currently with mixed outcomes reported even in cases with metastases. We herein report an additional case of EWSR1-PATZ1 fusion-related round cell sarcoma in the face of a 5-year-old boy with unusual histologic features of pale zones, rosette/gland-like structures and expression of epithelial markers. Fluorescent in-situ hybridization study (FISH) using EWSR1 breakapart probes was negative and molecular study with RNA sequencing was required to confirm the diagnosis. These findings highlight the diagnostic challenge and potential pitfall of FISH study in EWSR1-PATZ1 sarcoma. Further studies are required to increase the understanding of their behavior, morphologic spectrum and molecular features that will help devise new treatment strategies to these rare tumours.

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