Ranjan A, Chandy M J
Department of Neurological Sciences, Christian Medical College Hospital, Vellore, India.
Br J Neurosurg. 1994;8(2):179-85. doi: 10.3109/02688699409027964.
Although intrasellar tuberculomas have been reported in post-mortem examinations, they are exceptionally rare in clinical practice. Five patients with biopsy proven intrasellar tuberculoma with suprasellar extension are described. In four cases the clinical and radiological diagnosis was that of a pituitary adenoma. One patient, however, presented similar to a subarachnoid haemorrhage, but the CSF analysis was suggestive of tuberculous meningitis. All these patients presented either with intermittent headache or a sudden severe headache suggestive of an ictus. Hypopituitarism was diagnosed on clinical grounds in two patients and one patient had an associated galactorrhoea-amenorrhoea syndrome. Only one patient had a bitemporal field cut. In all other patients ophthalmological examination was normal. The CT scan showed a hyperdense sellar mass with suprasellar extension brightly enhancing with contrast in all cases. An angiogram in four patients did not reveal any vascular lesion. Laboratory investigation showed some degree of hypopituitarism in all cases. Transsphenoidal surgery was performed in four patients and operative findings were typical, and unlike those of a pituitary adenoma. All patients responded well to antituberculous treatment and at the end of 12 months were clinically and radiologically normal.
尽管在尸检中曾报告过鞍内结核瘤,但在临床实践中极为罕见。本文描述了5例经活检证实为鞍内结核瘤并向上扩展至鞍上的患者。其中4例患者的临床和影像学诊断为垂体腺瘤。然而,有1例患者表现类似蛛网膜下腔出血,但脑脊液分析提示结核性脑膜炎。所有这些患者均表现为间歇性头痛或突发剧烈头痛,提示发作。2例患者根据临床症状诊断为垂体功能减退,1例患者伴有溢乳-闭经综合征。仅1例患者有双颞侧视野缺损。所有其他患者眼科检查均正常。CT扫描显示所有病例均为鞍内高密度肿块,向上扩展至鞍上,增强扫描后明显强化。4例患者的血管造影未发现任何血管病变。实验室检查显示所有病例均有一定程度的垂体功能减退。4例患者接受了经蝶窦手术,手术所见具有典型性,与垂体腺瘤不同。所有患者对抗结核治疗反应良好,12个月末临床和影像学检查均恢复正常。