Oldring D, Fisch U
Am J Otol. 1979 Jul;1(1):7-18.
A series of 23 patients with glomus tumors of the temporal region, treated surgically at the ENT Department, University of Zurich, Switzerland from 1970 to 1977, is presented. A system of classification as to tumor size is described with tympanic, tympanomastoid, infralabyrinthine and intracranial tumors categorized as types A, B, C, and D respectively. A majority of tumors, 12 of 19 were infralabyrinthine (type C), and a surgical approach featuring permanent anterior displacement of the facial nerve, an cavity obliteration, has been employed with the aim of total tumor extirpation. There were five males in this series, with a mean age 22 years younger than for the females and all having infralabyrinthine (type C) tumors. The most frequent clinical presentation included pulsatile tinnitus, hearing loss, and observable tumor mass in the ear. Fifteen of 23 patients had significant hearing loss, of varying types on the tumor side, with one presenting as sudden hearing loss, and another as progressive unilateral sensorineural loss over several years, in the absence, initially, of tinnitus. Ten of 23 patients with type B, C, and D tumors had cranial nerve involvement, seven and tenth being the most frequent. Because of slow growth and tendency to multicentric origin, final conclusions cannot be made regarding treatment in such a recent series of cases. However, the impression gained suggests that radiotherapy is less effective than complete surgical excision, and that partial excision is to be avoided.
本文介绍了1970年至1977年期间在瑞士苏黎世大学耳鼻喉科接受手术治疗的23例颞部血管球瘤患者。描述了一种根据肿瘤大小的分类系统,其中鼓室、鼓室乳突、迷路下和颅内肿瘤分别归类为A、B、C和D型。大多数肿瘤(19例中的12例)为迷路下型(C型),并采用了一种以面神经永久性前移位和腔隙闭塞为特征的手术方法,旨在完全切除肿瘤。该系列中有5名男性,平均年龄比女性小22岁,且均患有迷路下型(C型)肿瘤。最常见的临床表现包括搏动性耳鸣、听力损失以及耳部可观察到的肿瘤肿块。23例患者中有15例有明显的听力损失,肿瘤侧的听力损失类型各异,其中1例表现为突发性听力损失,另1例在最初无耳鸣的情况下,数年来呈进行性单侧感音神经性听力损失。23例B、C和D型肿瘤患者中有10例出现颅神经受累,最常见的是第七和第十颅神经。由于肿瘤生长缓慢且有多发起源的倾向,对于这一近期病例系列的治疗无法得出最终结论。然而,所获得的印象表明,放疗的效果不如完全手术切除,并且应避免部分切除。