Tanaka Y, Hayashi S, Nakai M, Ryujin Y, Uematsu Y, Nakai K, Itakura T
Department of Neurosurgery, Minami Wakayama National Hospital.
No Shinkei Geka. 1995 Sep;23(9):801-6.
Intrasellar arachnoid cyst is very rare. We report a case of intrasellar arachnoid cyst. A 44-year-old male was admitted for evaluation of his headache and visual disturbance on August 6, 1993. Neurological examination revealed bilateral decreased visual acuity and visual field defect. Endocrinological examination showed panhypopituitarism. Other neurological findings were normal. X-ray film of the skull showed a ballooning dilation of the sella turcica with thinning of the sellar floor. CT scan showed a cystic lesion with CSF-density occupied the sella. After intravenous administration of contrast medium, the cyst showed no enhancement. MRI showed the intrasellar mass had the same characteristics as the surrounding subarachnoid space. Bilateral carotid angiographies demonstrated that the carotid siphons were stretched and displaced laterally, and the A1 portions of the anterior cerebral arteries were raised. We made a diagnosis of intrasellar cystic lesion. On August 18, the sella turcica was opened via the transsphenoidal rhinoseptal approach. The cyst contained CSF-like fluid, and a part of the cyst wall was resected. The cavity was filled with Gelfoam and the sellar floor was repaired with bone flap. Postoperatively, the patient's visual disturbance improved, but diabetis insipidus appeared and required hormonal replacement. The patient was discharged on September 27 with improvement of visual acuity and visual field. Histological examination demonstrated that the cyst wall consisted of thick arachnoidal cells with fibrous connective tissue. The arachnoidal cells with oval nuclei was stained with epithelial membrane antigen. Symptoms, signs and radiological findings of intrasellar arachnoid cyst are similar to those of various sellar lesions including pituitary adenoma, craniopharyngioma, empty sella, Rathke's cleft cyst, epidermoid et al.(ABSTRACT TRUNCATED AT 250 WORDS)
鞍内蛛网膜囊肿非常罕见。我们报告一例鞍内蛛网膜囊肿病例。一名44岁男性于1993年8月6日因头痛和视力障碍入院评估。神经系统检查发现双侧视力下降和视野缺损。内分泌检查显示全垂体功能减退。其他神经系统检查结果正常。头颅X线片显示蝶鞍呈气球样扩张,鞍底变薄。CT扫描显示一个脑脊液密度的囊性病变占据蝶鞍。静脉注射造影剂后,囊肿无强化。MRI显示鞍内肿块与周围蛛网膜下腔具有相同特征。双侧颈动脉血管造影显示颈动脉虹吸段被拉伸并向外侧移位,大脑前动脉A1段抬高。我们诊断为鞍内囊性病变。8月18日,经蝶窦鼻中隔入路打开蝶鞍。囊肿内含有类似脑脊液的液体,部分囊肿壁被切除。腔内填充明胶海绵,鞍底用骨瓣修复。术后,患者的视力障碍有所改善,但出现了尿崩症,需要激素替代治疗。患者于9月27日出院,视力和视野有所改善。组织学检查显示囊肿壁由厚的蛛网膜细胞和纤维结缔组织组成。椭圆形核的蛛网膜细胞被上皮膜抗原染色。鞍内蛛网膜囊肿的症状、体征和影像学表现与包括垂体腺瘤、颅咽管瘤、空蝶鞍、Rathke裂囊肿、表皮样囊肿等各种鞍区病变相似。(摘要截取自250字)