Suppr超能文献

滑膜肉瘤:一种罕见的喉部肿瘤。

Synovial sarcoma: a rare tumor of larynx.

作者信息

Bilgic Bilge, Mete Ozgür, Oztürk Settar A, Demiryont Misten, Keles Nesil, Basaran Mert

机构信息

Department of Pathology, Istanbul Medical Faculty, 34390 Istanbul, Turkey.

出版信息

Pathol Oncol Res. 2003;9(4):242-5. doi: 10.1007/BF02893385. Epub 2003 Dec 22.

Abstract

Synovial sarcoma is a soft tissue sarcoma of unknown histogenesis and occurs predominantly in the lower extremities of young adults. The head and neck is a relative rare location. There are about 10 cases with laryngeal localization in the literature. We present a 24 year-old male with an endolaryngeal mass. Incisional biopsy and the hemilaryngectomy material revealed a biphasic synovial sarcoma. One year later a local recurrence occurred. Tumor excision and neck dissection were performed. Radiotherapy was added. Six months later lung metastases was discovered on thoracic CT. The patient received chemotherapy for 6 courses. The metastases responded well to chemotherapy and the patient is now alive without tumor on radiological and clinical examination after 3.5 years of follow-up.

摘要

滑膜肉瘤是一种组织发生不明的软组织肉瘤,主要发生于年轻成年人的下肢。头颈部是相对少见的发病部位。文献中约有10例喉部滑膜肉瘤的报道。我们报告1例24岁男性患者,其喉部有一肿物。切开活检及半喉切除标本显示为双相型滑膜肉瘤。1年后出现局部复发,遂行肿瘤切除及颈部淋巴结清扫术,并加用放疗。6个月后胸部CT发现肺转移。患者接受了6个疗程的化疗。转移灶对化疗反应良好,随访3.5年后,经影像学和临床检查,患者目前存活且无肿瘤复发。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验