Geuna E, Pappadà G, Regalia F, Arrigoni M
Acta Neurochir (Wien). 1983;68(1-2):33-43. doi: 10.1007/BF01406200.
Multiple meningiomas are a seldom encountered neoplasm. Most authors report an incidence ranging from 1 to 3% of all meningiomas. The routine use of CT has resolved diagnostic problems involved with multiple meningiomas; nevertheless, they still present several nosologic problems. In fact, it may be difficult to differentiate "true multiple meningiomas", defined as a distinct entity by Cushing in 1938, from simple recurrences or the special variant (forme fruste) of von Recklinghausen's disease. Our report deals with nine cases of multiple meningiomas selected from a series of 372 meningiomas operated from 1968 to 1981 at our hospital. Cases were divided into a) multiple simultaneous meningiomas (five cases), b) multiple meningiomas successively detected at different localizations (two cases), and c) multiple meningiomas associated with neurofibromatosis (two cases). Only five of these nine cases, four from the first group and one from the second, were true multiple meningiomas. Pathogenetic factors related to true multiple meningiomas are discussed in relation to the literature reports. However, the different hypotheses proposed do not offer a definite explanation of the multicentricity of these tumours.
多发性脑膜瘤是一种罕见的肿瘤。大多数作者报告其发病率占所有脑膜瘤的1%至3%。CT的常规使用解决了与多发性脑膜瘤相关的诊断问题;然而,它们仍然存在一些分类学问题。事实上,可能难以将1938年由库欣定义为一种独特实体的“真正的多发性脑膜瘤”与简单复发或冯·雷克林豪森病的特殊变体(顿挫型)区分开来。我们的报告涉及从1968年至1981年在我院接受手术的372例脑膜瘤系列中选取的9例多发性脑膜瘤病例。病例分为:a)多发性同时性脑膜瘤(5例),b)在不同部位先后检测到的多发性脑膜瘤(2例),以及c)与神经纤维瘤病相关的多发性脑膜瘤(2例)。这9例病例中只有5例是真正的多发性脑膜瘤,其中4例来自第一组,1例来自第二组。结合文献报道讨论了与真正的多发性脑膜瘤相关的发病因素。然而,所提出的不同假说并未对这些肿瘤的多中心性给出明确解释。