Fukuda I, Ogasawara H, Kumoi T, Sugihara K, Wada H
Department of Otolaryngology, Hyogo College of Medicine, Japan.
Int J Pediatr Otorhinolaryngol. 1987 Dec;14(2-3):161-70. doi: 10.1016/0165-5876(87)90027-9.
Reported here for the first time is a case of subglottic neurofibroma in an infant which was removed by laryngofissure. Neurofibromas are ubiquitous in distribution, but very rare in the larynx and also extremely rare in infancy. Only 9 cases had been reported in children under 9 years of age. In the present case, H.T., a boy aged 2 years and 7 months, complaining of inspiratory stridor since the beginning of December 1985, was admitted to our hospital on Jan. 21, 1986. The tumor was completely removed by laryngofissure and pathological diagnosis showed it to be a neurofibroma. Laryngeal neurofriboma cases are reviewed and discussed.
本文首次报道了1例婴儿声门下神经纤维瘤,通过喉裂开术将其切除。神经纤维瘤分布广泛,但在喉部非常罕见,在婴儿期更是极为罕见。9岁以下儿童仅报道过9例。在本病例中,患儿H.T.,男,2岁7个月,自1985年12月初起出现吸气性喘鸣,于1986年1月21日入院。通过喉裂开术将肿瘤完全切除,病理诊断显示为神经纤维瘤。本文对喉神经纤维瘤病例进行了回顾和讨论。