一名 TP53 基因突变患者的高级别转移性多形性横纹肌肉瘤:成人罕见病例

Shervin Zoghi, Aaron Tsumura, Rashmi Verma, Morgan Angus Darrow
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引用次数: 0

摘要

成人多形性横纹肌肉瘤(PRMS)是一种异常罕见的侵袭性软组织肿瘤,由未分化的间充质细胞引起。成人横纹肌肉瘤虽然在儿童中更为常见,但预后较差,需要立即进行积极干预。在此,我们介绍了一例左大腿高级别多形性横纹肌肉瘤病例,患者为一名 58 岁男性,肿瘤已转移至肺部和盆腔。由于这种罕见疾病和亚型的诊断和治疗方案有限,本病例研究的目的是强调治疗这种疾病的综合临床方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-Grade Metastatic Pleomorphic Rhabdomyosarcoma in a TP53 Germline Mutation Patient: A Rare Presentation in Adults
Pleomorphic Rhabdomyosarcomas (PRMS) in adults are an exceptionally rare and aggressive soft-tissue tumor arising from undifferentiated mesenchymal cells. While more common in children, rhabdomyosarcomas in adults are associated with poorer outcomes and require immediate, aggressive intervention. Here we present a case of high-grade pleomorphic rhabdomyosarcoma of the left thigh in a 58-year-old male with metastases to the lungs and pelvis. Due to the limited diagnostic and treatment protocols of this rare disease and subtype, the goal of this case study is to highlight a comprehensive clinical approach to this disease.
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