罕见的声门型多形性横纹肌肉瘤：一例报告并文献复习
Rare Glottic Pleomorphic Rhabdomyosarcoma: A Case Report with Review of Literature.
作者信息
Kumar Manoj, Sekhon Pahaul, Singh Rohit
机构信息
Department of ENT, Command Hospital (SC), Pune, India.
Department of ENT, Armed Forces Medical College, Pune, India.
出版信息
Indian J Otolaryngol Head Neck Surg. 2024 Aug;76(4):3652-3655. doi: 10.1007/s12070-024-04665-0. Epub 2024 Apr 6.
Abstract
Rhabdomyosarcoma (RMS) is commonly reported in children and very rarely in adults. Laryngeal RMS is a rare but extremely aggressive malignancy with a high mortality rate. Surgery followed by postoperative radiotherapy is the preferred treatment. The use of chemotherapy is debatable. This report highlights a case of rare pleomorphic rhabdomyosarcoma of glottis in a 67-year-old male who presented with hoarseness and a description of its management.
摘要
横纹肌肉瘤（RMS）常见于儿童，在成人中极为罕见。喉横纹肌肉瘤是一种罕见但极具侵袭性的恶性肿瘤，死亡率很高。手术加术后放疗是首选治疗方法。化疗的使用存在争议。本报告重点介绍了一名67岁男性发生的罕见的声门多形性横纹肌肉瘤病例，该患者表现为声音嘶哑，并描述了其治疗情况。
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