Nagao S, Kawai N, Ohomoto T, Oohashi T
Department of Neurological Surgery, Kagawa Medical School.
No Shinkei Geka. 1990 Jul;18(7):637-42.
A case of intrasellar and suprasellar meningioma with hypopituitarism is reported. A-64-year-old woman was admitted to our hospital with chief complaints of reduced consciousness and inactivity. She had a history of subarachnoid hemorrhage 20 years previously, and developed right third nerve palsy. Physical examination demonstrated that, in consciousness, she was stuporous, and she had impaired visual acuity and palsy in the right third nerve. An X-ray film of the sella turcica showed enlargement and intrasellar calcification. A CT scan with contrast enhancement revealed a homogenously enhanced mass in the sella and suprasellar region. A cerebral angiogram showed elevation of the bilateral A1 portion of the anterior cerebral artery. No tumor blush was evident. Endocrinologic function tests confirmed impaired anterior lobe hormones and hypothyroidism. Preoperative diagnosis was pituitary adenoma. The tumor was subtotally removed by using the transsphenoidal approach and right frontotemporal craniotomy was carried out using microsurgery in a two staged operation. The tumor was yellowish-grey, partly firm in consistency, and it had a soft elasticity. Operative findings showed that the dura matter of the tuberculum sella, the anterior and posterior clinoid process, the medial sphenoidal ridge, and the wall of the cavernous sinus were intact, which was confirmed at autopsy, later. Microscopical examination revealed a mixed meningothelial and fibroblastic meningioma with papillary component and psammomatous bodies. The tumor was thought to originate in the diaphragma sella, and to extend in intrasellar and suprasellar directions. The patient died of basilar artery thrombosis. In clinical and radiological examination, there is no definite difference between pituitary adenoma and intrasellar meningioma.(ABSTRACT TRUNCATED AT 250 WORDS)
报告一例伴有垂体功能减退的鞍内及鞍上脑膜瘤病例。一名64岁女性因意识减退和活动减少为主诉入院。她20年前有蛛网膜下腔出血病史,并出现右侧动眼神经麻痹。体格检查发现,意识方面,她处于昏睡状态,视力受损且右侧动眼神经麻痹。蝶鞍X线片显示蝶鞍扩大及鞍内钙化。增强CT扫描显示鞍内及鞍上区域有均匀强化的肿块。脑血管造影显示双侧大脑前动脉A1段抬高。未见肿瘤染色。内分泌功能检查证实前叶激素受损及甲状腺功能减退。术前诊断为垂体腺瘤。采用经蝶窦入路行肿瘤次全切除,并分两期进行显微手术的右侧额颞开颅术。肿瘤呈黄灰色,部分质地硬,有软弹性。手术所见显示蝶鞍结节、前后床突、蝶骨嵴内侧及海绵窦壁的硬脑膜完整,后来尸检证实。显微镜检查显示为混合性脑膜内皮型和纤维母细胞型脑膜瘤,伴有乳头成分及砂粒体。肿瘤被认为起源于鞍隔,向鞍内及鞍上方向延伸。患者死于基底动脉血栓形成。在临床和影像学检查中,垂体腺瘤和鞍内脑膜瘤之间没有明确差异。(摘要截短至250字)