Iwabuchi S, Tanita T, Koike K, Fujimura S
Department of Surgery, Tohoku University, Sendai, Japan.
Surg Today. 1993;23(9):816-9. doi: 10.1007/BF00311626.
We report herein a case of familial neurilemmomatosis seen in a 16-year-old girl and her 38-year-old mother. The girl presented to us with an intrathoracic vagal neurilemmoma, as well as neurilemmomas on the right fifth intercostal nerve and in the serratus anterior muscle. Two years after these tumors were resected, bilateral acoustic neuromas and multiple brain stem tumors appeared. Her mother was being treated simultaneously at another hospital for multiple neurilemmomas, including bilateral acoustic neurilemmomas, suggesting the possibility that neurilemmomatosis is an autosomal dominantly inherited disorder.
我们在此报告一例发生在一名16岁女孩及其38岁母亲身上的家族性神经鞘瘤病。该女孩因胸腔内迷走神经神经鞘瘤、右第五肋间神经和前锯肌神经鞘瘤前来就诊。这些肿瘤切除两年后,出现了双侧听神经瘤和多个脑干肿瘤。她的母亲正在另一家医院同时接受多种神经鞘瘤的治疗,包括双侧听神经鞘瘤,这表明神经鞘瘤病可能是一种常染色体显性遗传性疾病。