Meis J M, Mackay B, Goepfert H
Arch Otolaryngol Head Neck Surg. 1986 Dec;112(12):1289-92. doi: 10.1001/archotol.1986.03780120053010.
Primary liposarcoma of the larynx is extremely rare. To our knowledge, only eight cases have been documented in the English literature. We report a ninth case in a 54-year-old man. The recurrent 2-cm tumor was well differentiated and was treated with a supraglottic laryngectomy with partial neck dissection followed by radiotherapy. There has not been a second recurrence in 16 months. The majority of liposarcomas arising in the larynx have been of a favorable histologic type (well differentiated or myxoid). The tumor tends to occur in a supraglottic location in men of 40 years or more, and multiple recurrences are typical. The primary mode of treatment is wide surgical excision, with or without postoperative radiation therapy.
喉原发性脂肪肉瘤极为罕见。据我们所知,英文文献中仅记载了8例。我们报告1例发生于一名54岁男性的第9例病例。复发性2厘米肿瘤分化良好,行声门上喉切除术加部分颈部清扫术,术后辅以放疗。16个月来未出现二次复发。发生于喉部的大多数脂肪肉瘤组织学类型良好(高分化或黏液样)。肿瘤倾向于发生在40岁及以上男性的声门上部位,且多次复发很常见。主要治疗方式为广泛手术切除,可辅以或不辅以术后放射治疗。