口咽及下咽黏液瘤：病例报告及文献综述
Oropharyngeal and hypopharyngeal myxoma: case report and literature review.
作者信息
Ayache S, Chatelain D, Tramier B, Strunski V
机构信息
ORL and Head and Neck Surgery Department, General Hospital, Mont de Marsan, University Hospital of Amiens, France.
出版信息
J Laryngol Otol. 2007 May;121(5):e5. doi: 10.1017/S002221510700669X. Epub 2007 Apr 3.
OBJECTIVES
To describe the features of an oropharyngeal and hypopharyngeal myxoma.
MATERIALS AND METHODS
Case report of a 34-year-old patient operated upon for a dual-location tumour, and review of the literature.
RESULTS
The myxoma is a rare tumour. Various head and neck locations have been described, but not (to our knowledge) a tumour in both the oropharynx and the hypopharynx. Multiple synchronous locations must be searched for, particularly regarding cardiac myxoma.
CONCLUSION
The myxoma is a rare, benign tumour, even rarer in the head and neck. Surgical treatment must be complete in order to avoid recurrences, and should be performed after assessment for cardiac involvement.
目的
描述口咽和下咽黏液瘤的特征。
材料与方法
报告一例34岁因双部位肿瘤接受手术治疗的患者病例，并进行文献复习。
结果
黏液瘤是一种罕见肿瘤。文献中描述过其在头颈部的不同部位，但据我们所知，尚无口咽和下咽同时发生肿瘤的报道。必须查找是否存在多个同步发病部位，尤其是心脏黏液瘤。
结论
黏液瘤是一种罕见的良性肿瘤，在头颈部更为罕见。手术治疗必须彻底以避免复发，且应在评估是否存在心脏受累后进行。
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