Case Report: An NTRK1 fusion-positive embryonal rhabdomyosarcoma: clinical presentations, pathological characteristics and genotypic analyses

Case Report: An NTRK1 fusion-positive embryonal rhabdomyosarcoma: clinical presentations, pathological characteristics and genotypic analyses

Rhabdomyosarcoma (RMS) is a prevalent form of soft tissue sarcoma that primarily affects children. Pediatric RMS is characterized by two distinct histological variants: embryonal (ERMS) and alveolar (ARMS). ERMS is a malignant tumor with primitive characteristics resembling the phenotypic and biolog...

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Bibliographic Details
Main Authors: Na-Mei Li, Shi-He Jiang, Peng Zhou, Xiao-Hong Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-04-01
Series:Frontiers in Oncology
Subjects:
embryonal rhabdomyosarcoma
NTRK1 fusion
case report
pathological features
next generation sequencing (NGS)
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2023.1178945/full

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