Rakheja Dinesh, Park Jason Y, Yang Mary S, Martinez Diana P, Koduru Prasad, Wilson Kathleen S, Garcia Rolando, Uddin Naseem
Department of Pathology, 12334University of Texas Southwestern Medical Center, Dallas, TX, USA.
Children's Health, Dallas, TX, USA.
Int J Surg Pathol. 2023 Apr;31(2):213-220. doi: 10.1177/10668969221098084. Epub 2022 May 3.
Epithelioid rhabdomyosarcoma is a rare rhabdomyosarcoma variant for which no diagnostic recurrent driver genetic events have been identified. Here we report a rapidly progressive and widely metastatic rhabdomyosarcoma with epithelioid features that arose in the thigh of a male infant. Conventional cytogenetics revealed a t(8;13)(p11.2;q14) translocation. Fluorescence in situ hybridization studies showed rearrangement of and amplification of its 3" end, and rearrangement of and amplification of its 5` end. Next generation sequencing identified a fusion, which is a previously unreported gene fusion. We also review the historic report of a fusion in a solid variant of alveolar rhabdomyosarcoma and propose that fusion may have been the more appropriate interpretation of the data presented in that report.
上皮样横纹肌肉瘤是一种罕见的横纹肌肉瘤变体,尚未发现诊断性复发性驱动基因事件。在此,我们报告一例发生于男婴大腿的具有上皮样特征的快速进展且广泛转移的横纹肌肉瘤。常规细胞遗传学显示存在t(8;13)(p11.2;q14)易位。荧光原位杂交研究显示其3'端重排并扩增,5'端重排并扩增。下一代测序鉴定出一种融合,这是一种先前未报道的基因融合。我们还回顾了肺泡横纹肌肉瘤实体变体中融合的历史报告,并提出融合可能是该报告中所呈现数据的更恰当解释。