Mobashir Mohammad Kamal, Mohamed Abd ElRaof Said, El-Anwar Mohammad Waheed, El Sayed Ahmad Ebrahim, Fouad Mouhamad A
Department of Otorhinolaryngology-Head and Neck Surgery, Zagazig University, Zagazig, Egypt.
Department of Pathology, Zagazig University, Zagazig, Egypt.
Int Arch Otorhinolaryngol. 2015 Oct;19(4):349-53. doi: 10.1055/s-0034-1396793. Epub 2014 Dec 12.
Introduction Laryngeal neurofibromas are extremely rare, accounting for only 0.03 to 0.1% of benign tumors of the larynx. Objectives To report the first case of massive neck plexiform neurofibroma with intralaryngeal (supraglottic) extension in a 5-year-old boy with neurofibromatosis type 1 and to describe its treatment. Resumed Report This massive plexiform neurofibroma was surgically removed, relieving its significant respiratory obstructive symptoms without recurrence to date. Conclusion Massive neck plexiform neurofibroma with supraglottic part was found in a child with neurofibromatosis type 1; it should be included in differential diagnosis of stridor and neck mass in children. It was diagnosed and removed in early in childhood without recurrence.
喉神经纤维瘤极为罕见,仅占喉部良性肿瘤的0.03%至0.1%。目的:报告首例1型神经纤维瘤病5岁男孩发生的伴有喉内(声门上)扩展的巨大颈部丛状神经纤维瘤病例,并描述其治疗方法。病例报告:该巨大丛状神经纤维瘤经手术切除,缓解了严重的呼吸阻塞症状,迄今为止未复发。结论:在1型神经纤维瘤病患儿中发现了伴有声门上部分的巨大颈部丛状神经纤维瘤;应将其纳入儿童喘鸣和颈部肿块的鉴别诊断中。该病例在儿童早期得到诊断并切除,未复发。