El Shennawy M, Khafagy M, Ishak E
J Laryngol Otol. 1980 Jun;94(6):677-82. doi: 10.1017/s0022215100089416.
Embryonal rhabdomyosarcoma is a rare condition that tends to occur in the head and neck in children. This disease carried a very poor prognosis until 10 years ago when a multidisciplinary approach (with surgery, therapy and multiple drug chemotherapy) was instituted. In this article a review of the literature on embryonal rhabdomyosarcoma is given and three rare cases have been reported; the first involved the palate, the second affected the ear and mastoid, and the third was a case originating in the nasopharynx with orbital involvement. Clinical and histopathological descriptions are given and the results of therapy are evaluated.
胚胎性横纹肌肉瘤是一种罕见疾病,多见于儿童的头颈部。直到10年前采用多学科方法(手术、放疗和多药化疗)之前,这种疾病的预后都非常差。本文对胚胎性横纹肌肉瘤的文献进行了综述,并报告了3例罕见病例;第一例累及腭部,第二例影响耳部和乳突,第三例起源于鼻咽部并累及眼眶。给出了临床和组织病理学描述,并对治疗结果进行了评估。