Bernreuther Christian, Flitsch Jörg, Lüdecke Dieter K, Hagel Christian
Brain Pathol. 2008 Apr;18(2):283-7. doi: 10.1111/j.1750-3639.2008.00158.x.
The case of a 61-year-old man presenting with dizziness, nausea, vomiting, reduced serum osmolality, and hyponatremia is reported. Endocrinologically, low levels for ADH, cortisol and testosterone as well as low-normal values for ACTH, LH and FSH were detected. Cranial computed tomography and MRI scans revealed an intra- and suprasellar tumor of adenoma-like appearance with elevation of the optic chiasm. No infiltration of the cavernous sinus was seen. After transsphenoidal resection of the tumor, no additional anterior lobe insufficiencies or diabetes insipidus occurred. Histological examination revealed a tumor consisting of spindle-shaped cells of uniformly high cellularity with no evidence of hypocellular areas. A cellular schwannoma was diagnosed. An intrasellar cellular schwannoma clinically and radiologically mimicking a non-secreting pituitary adenoma is uncommon. However, rare entities like schwannomas, melanocytomas or pituicytomas have to be considered in addition to the more common tumors like pituitary adenomas and meningiomas.
报告了一名61岁男性患者,出现头晕、恶心、呕吐、血清渗透压降低和低钠血症的病例。在内分泌方面,检测到抗利尿激素(ADH)、皮质醇和睾酮水平较低,促肾上腺皮质激素(ACTH)、促黄体生成素(LH)和促卵泡生成素(FSH)为低正常水平。头颅计算机断层扫描(CT)和磁共振成像(MRI)显示鞍内和鞍上有腺瘤样外观的肿瘤,视交叉抬高。未见海绵窦受侵。肿瘤经蝶窦切除后,未出现额外的前叶功能不全或尿崩症。组织学检查显示肿瘤由细胞均匀密集的梭形细胞组成,无细胞减少区域的证据。诊断为细胞性神经鞘瘤。鞍内细胞性神经鞘瘤在临床和放射学上模拟无分泌功能的垂体腺瘤并不常见。然而,除了更常见的肿瘤如垂体腺瘤和脑膜瘤外,还必须考虑神经鞘瘤、黑素细胞瘤或垂体细胞瘤等罕见实体。