LARYNGEAL SYNOVIAL SARCOMA – A CASE REPORT

A. N. Vlăescu, E. Ioniță, Andreea Nicoleta Vlăescu, F. Anghelina, I. Ioniță, C. Mogoantă, M. Ciolofan
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引用次数: 0

Abstract

Laryngeal synovial sarcoma is an extremely rare mesenchymal tumor. During the past four decades, literature findings revealed under 40 cases with this localization. We are bringing forward the case of a 70-year-old male patient who was referred to the ENT Clinic as a respiratory emergency – a tumor obstructing the laryngeal glottis, for which an emergency tracheotomy was initially performed, followed by a CT scan and a biopsy under general anesthesia through suspension videolaringoscopy. The histopathological report was suggestive of a biphasic synovial sarcoma. A multidisciplinary team set the surgical indication for total laryngectomy followed by chemo-radiotherapy. Long-term follow-up is mandatory for recurrence prevention. Patient has checked in for follow-up every 3 months over the past 2 years, with no macroscopic signs of tumoral relapse.
喉滑膜肉瘤1例报告
摘要喉滑膜肉瘤是一种极为罕见的间充质肿瘤。在过去的四十年中,文献发现有这种定位的病例不到40例。我们提出一个70岁的男性病人,他被转诊到耳鼻喉科作为呼吸急症——一个肿瘤阻塞喉声门,最初进行了紧急气管切开术,随后进行了CT扫描,并在全身麻醉下通过悬吊式视屏镜检进行了活检。组织病理学报告提示为双期滑膜肉瘤。一个多学科团队确定了全喉切除术后化疗的手术指征。长期随访是预防复发的必要措施。患者2年内每3个月随访一次,无肿瘤复发的宏观征象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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