Pinzer Th, Krishnan K G, Schackert G
Department of Neurosurgery, Carl Gustav Carus University Hospital, Dresden, Germany.
Zentralbl Neurochir. 2004 Nov;65(4):195-7. doi: 10.1055/s-2004-822785.
It is important to differentiate the rare Diaphragma sellae meningioma from the quite common hormonally inactive pituitary adenoma, especially with regards to the surgical approach. The differentiation could, however, be problematic. We report the case of a 66-year-old woman with a Diaphragma sellae meningioma, which became apparent through a visual field and visual acuity disorder. Successful radical tumor extirpation was achieved via the transsphenoidal approach, since the space-occupying lesion was initially thought to be a hormonally inactive pituitary macroadenoma. However, histological investigation confirmed a meningioma. A careful retrospective analysis of the MRI revealed the possibility of a meningioma having been overlooked, since not all distinguishing features of this lesion were manifested. These criteria, as well as the principles of the surgical approach for treating sellar space-occupying lesions are discussed.
将罕见的鞍膈脑膜瘤与相当常见的无激素活性垂体腺瘤区分开来很重要,尤其是在手术入路方面。然而,这种区分可能存在问题。我们报告了一例66岁患有鞍膈脑膜瘤的女性病例,该病例通过视野和视力障碍得以发现。由于最初认为占位性病变是无激素活性的垂体大腺瘤,因此通过经蝶窦入路成功实现了肿瘤的根治性切除。然而,组织学检查证实为脑膜瘤。对磁共振成像(MRI)进行仔细的回顾性分析发现,有可能漏诊了脑膜瘤,因为该病变的所有鉴别特征并未都表现出来。本文讨论了这些标准以及治疗鞍区占位性病变的手术入路原则。