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Intraparotid facial nerve plexiform neurofibroma in a child (case report)

机译:儿童肺炎面部神经丛斑神经纤维瘤(案例报告)

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BackgroundIntraparotid facial nerve neurofibromas are benign neoplasms, extremely rare, difficult to diagnose and to manage. Only three pediatric cases have been reported in the literature.Case presentationWe report the 4th case of a 7-year-old child admitted for a parotid mass without facial palsy, for whom the surgical indication was the increase in volume of this mass, as well as the aesthetical impairment, the surgical exploration found the tumor attached to the lower branch of the division of the facial nerve. The excision of the mass was performed with the sacrifice of the inferior branch of the facial nerve, the trunk and the upper branch of the facial nerve was preserved, the pathological study was in favor of a plexiform neurofibroma.The patient has presented postoperatively a grade 5 facial palsy in the inferior territory of the facial nerve with a slight recovery 1 year after surgery.ConclusionEven though plexiform neurofibromas in the parotid gland are extremely rare, and their diagnosis are not often primary evoked in front of any growing mass of this region, the surgeon must keep in mind the existence of these neoplasms as a differential diagnosis of a parotid tumor.
机译:BackgroundIntraparotid面神经神经神经神经纤维纤维瘤是良性肿瘤,极其罕见,难以诊断和管理。在文献中仅报告了三个儿科案例。Case展示我们报告了一个7岁儿童的第四个案例,其中一个没有面部麻痹的腮腺菌菌群,外科迹象是该群众体积的增加,也是如此作为审美损害,外科探索发现肿瘤附着在面神经分裂的下分支。在面神经的牺牲中牺牲了肿块的切除,躯干和面部神经的上枝被保存,病理学研究有利于丛状神经纤维瘤。患者术后呈现了级别5个面神经在面部神经的劣质境内,手术后1年略有恢复。静脉曲张的神经纤维瘤在腮腺中的七斑神经纤维瘤非常罕见,并且它们的诊断通常在该地区的任何日益大量群体前初前诱发,外科医生必须牢记这些肿瘤的存在作为腮腺肿瘤的差异诊断。

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