Abs R, Parizel P M, Willems P J, Van de Kelft E, Verlooy J, Mahler C, Verhelst J, Van Marck E, Martin J J
Department of Endocrinology, University of Antwerp, Belgium.
Eur Neurol. 1993;33(6):416-22. doi: 10.1159/000116986.
Seven patients with the co-occurrence of meningioma and pituitary adenoma are reported. Diagnosis was based on histological examination and if not available on MR imaging. Extensive review of the literature reveals only 18 other cases with this association if meningiomas appearing after radiation therapy for pituitary tumors are excluded. As in isolated meningiomas, the female-to-male ratio is high. A preponderance of perisellar meningiomas is apparent. Another distinct characteristic of this combination is not revealed, since no specific typing of the meningioma and no specific endocrine syndrome is uncovered. Two patients presented with multiple meningiomas, of which one showed two histologically different tumor types. The presence of other tumors in association with pituitary adenomas and meningiomas in our series is striking and could suggest a genetic dysregulation leading to the development of these tumors.
本文报告了7例同时患有脑膜瘤和垂体腺瘤的患者。诊断基于组织学检查,若无法进行组织学检查,则依据磁共振成像。对文献进行广泛回顾后发现,若排除垂体瘤放射治疗后出现的脑膜瘤,仅有另外18例此类关联病例。与孤立性脑膜瘤一样,女性与男性的比例较高。鞍旁脑膜瘤占优势较为明显。由于未发现脑膜瘤的具体类型及特定的内分泌综合征,因此尚未揭示这种组合的另一个显著特征。两名患者出现多发性脑膜瘤,其中一名患者的肿瘤在组织学上显示为两种不同类型。在我们的系列病例中,垂体腺瘤和脑膜瘤合并其他肿瘤的情况显著,这可能提示存在导致这些肿瘤发生的基因失调。