Danninger R, Humer U, Stammberger H
Hals-Nasen-Ohren Universitätsklinik Graz.
Laryngorhinootologie. 1994 Aug;73(8):442-4. doi: 10.1055/s-2007-997169.
The synovial sarcoma of the larynx is a very rare tumour. Only six cases have been published so far in international literature. We describe a synovial sarcoma of the larynx in a 53-year old patient. Laryngectomy and neck-dissection were performed, followed by adjuvant radiotherapy. 16 months after therapy neither locoregional recurrence nor lung metastases have occurred. Clinically, an attempt can be made to differentiate a synovial sarcoma from a squamous cell carcinoma based on the appearance of the surface epithelium. It is still a problem to safely establish the diagnosis of a synovial sarcoma on the basis of a biopsy. The poor prognosis of this tumour requires radical surgical removal. The effects of radiation are discussed controversially.
喉滑膜肉瘤是一种非常罕见的肿瘤。迄今为止,国际文献中仅发表过6例。我们描述了一名53岁患者的喉滑膜肉瘤。患者接受了喉切除术和颈部清扫术,随后进行辅助放疗。治疗16个月后,未出现局部区域复发和肺转移。临床上,可以根据表面上皮的外观尝试将滑膜肉瘤与鳞状细胞癌区分开来。基于活检安全地确诊滑膜肉瘤仍然是一个问题。该肿瘤预后较差,需要进行根治性手术切除。关于放疗的效果存在争议。