Koh Y C, Yoo H, Whang G C, Kwon O K, Park H I
Department of Neurosurgery, Inje University Seoul Paik Hospital, Seoul, Korea.
J Clin Neurosci. 2001 May;8 Suppl 1:40-3. doi: 10.1054/jocn.2001.0875.
Meningioma is a common intracranial tumour and it may occur not infrequently as one of the multiple tumours, especially in patients with neurofibromatosis. The incidence of multiple meningiomas (MMs) without the stigmata of neurofibromatosis is rare, ranging from 1 to 9% of all meningiomas in the literature. Multiple meningiomas with different pathologic features are even rarer, and most of them are benign histologies. The authors report an extremely rare case of MMs which were presented with malignant and benign histological features simultaneously. The underlying mechanism of MM formation is still unclear, however, subarachnoid spread was thought to be the most likely mechanism. The findings of most of MMs showed identical histopathological features and several molecular biologic studies provided evidence for the monoclonal origin of MMs to back up the above hypothesis. However, different histological features among the reported multiple meningioma cases including our particular one, suggests their origin from multicentric neoplastic foci activated by a supposed tumour-producing factor. However, we cannot completely exclude the possibility of independent progression from monoclonal origin.
脑膜瘤是一种常见的颅内肿瘤,它作为多发肿瘤之一并不少见,尤其是在神经纤维瘤病患者中。无神经纤维瘤病特征的多发脑膜瘤(MMs)发病率很低,在文献中占所有脑膜瘤的1%至9%。具有不同病理特征的多发脑膜瘤更为罕见,且大多数为良性组织学类型。作者报告了1例极其罕见的多发脑膜瘤病例,其同时具有恶性和良性组织学特征。多发脑膜瘤形成的潜在机制仍不清楚,然而,蛛网膜下腔播散被认为是最可能的机制。大多数多发脑膜瘤的研究结果显示出相同的组织病理学特征,一些分子生物学研究为多发脑膜瘤的单克隆起源提供了证据,以支持上述假设。然而,包括我们这个特殊病例在内的已报道多发脑膜瘤病例中的不同组织学特征,提示它们起源于由假定的肿瘤产生因子激活的多中心肿瘤病灶。然而,我们不能完全排除从单克隆起源独立进展的可能性。