Watanabe M, Toyama M, Watanabe M, Taniguchi Y, Kaneko K, Yokoyama M
Department of Neurosurgery, Nagaoka Red Cross Hospital, Japan.
No Shinkei Geka. 1987 Aug;15(8):869-74.
A case of intrasellar meningioma is reported. A 49-year-old woman was admitted to our hospital on July 22, 1985, complaining of reduced visual acuity and visual field defect. Visual acuity was 0.6 in the right eye and 0.1 in the left eye. Visual field examination revealed upper temporal quadrantanopsia on the right side and incomplete temporal hemianopsia on the left side. Ocular fundi were normal. X-ray films of the skull showed a balloon-shaped sella turcica with "double floor". CT scan showed a isodense mass with central low density occupying the intrasellar and suprasellar region. After administration of contrast medium, almost homogenous enhancement was noted. Bilateral carotid angiographies demonstrated that horizontal portion of the right anterior cerebral artery was raised. No tumor blush was evident. Endocrinologic function tests confirmed a complete deficit of the anterior lobe hormones except for elevated serum prolactin level of 110 ng/ml. She showed no galactorrhea. On August 6, 1985, the sella turcica was reached via the transsphenoidal rhinoseptal approach. The sella floor and dura matter were intact. The grey, soft and necrotic tumor tissue was encountered and bleeding was controllable. The tumor extending to suprasellar region was firm in consistency. Pathologically, the tumor was a typical meningothelial meningioma. Postoperatively, visual field defect improved and visual acuity was recovered on the right side immediately. Postoperative CT scan showed a thin residual enhanced lesion, which was the attachment of the tumor. It seemed to be the elevated diaphragma sellae. Clinical observation, radiological and endocrinological findings of intrasellar meningioma are similar to that of non-functioning pituitary adenoma.(ABSTRACT TRUNCATED AT 250 WORDS)
报告1例鞍内脑膜瘤。1985年7月22日,一名49岁女性因视力下降和视野缺损入住我院。右眼视力0.6,左眼视力0.1。视野检查显示右侧颞上象限盲,左侧不完全颞侧偏盲。眼底正常。头颅X线片显示蝶鞍呈气球状,有“双底”。CT扫描显示等密度肿块,中央低密度,占据鞍内和鞍上区域。注入造影剂后,可见几乎均匀强化。双侧颈动脉血管造影显示右大脑前动脉水平段抬高。未见肿瘤染色。内分泌功能检查证实除血清催乳素水平升高至110 ng/ml外,前叶激素完全缺乏。她无溢乳现象。1985年8月6日,经经蝶窦鼻中隔入路到达蝶鞍。蝶鞍底和硬脑膜完整。遇到灰白色、柔软且坏死的肿瘤组织,出血可控。延伸至鞍上区域的肿瘤质地坚硬。病理检查显示,该肿瘤为典型的脑膜内皮型脑膜瘤。术后,视野缺损改善,右侧视力立即恢复。术后CT扫描显示一薄层强化残留病变,为肿瘤附着处。似乎是抬高的鞍隔。鞍内脑膜瘤的临床观察、影像学和内分泌学表现与无功能垂体腺瘤相似。(摘要截短至250字)