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垂体非特异性肉芽肿:6例手术治疗报告

Non-specific granulomas of the pituitary: report of six cases treated surgically.

作者信息

Oeckler R C, Bise K

机构信息

Neurosurgical Clinic, Ludwig-Maximilian University of Munich, Fed. Rep. of Germany.

出版信息

Neurosurg Rev. 1991;14(3):185-90. doi: 10.1007/BF00310655.

Abstract

Granulomatous lesions of the pituitary gland are very rare. In our department, six patients with these lesions have been operated on since 1988. The records of these patients were analysed and are reported in the following. Three of the patients were admitted because of severe and rapid development of visual disturbances caused by a suprasellar extending lesion. Endocrinological examination most often found posterior lobe insufficiency, was followed by anterior lobe dysfunction. CT and MRI demonstrated a cystic lesion with semiliquid content, where mild contrast enhancement of the walls of the tumor was observed in all cases. Surgery was performed using the transphenoidal approach. Rapid relief of visual impairment was observed in the three patients with chiasmal compression. In one patient, recurrent chiasm syndrome due to lesion regrowth required additional surgery with transcranial resection of the capsule. Unfortunately, visual impairment persisted postoperatively in one eye. Endocrinological follow-up demonstrated unchanged or even worsened pituitary functions in all cases. Our study revealed no consistent predictive preoperative finding. Therefore, we consider an indication for decompression surgery to be given in all patients with chiasmal syndrome and for diagnostic surgery for all patients with intrasellar lesions.

摘要

垂体肉芽肿性病变非常罕见。自1988年以来,我科已对6例患有此类病变的患者进行了手术。对这些患者的记录进行了分析,并报告如下。其中3例患者因鞍上扩展病变导致严重且迅速发展的视力障碍而入院。内分泌检查最常发现垂体后叶功能不全,其次是垂体前叶功能障碍。CT和MRI显示为含有半液体内容物的囊性病变,所有病例均观察到肿瘤壁有轻度强化。采用经蝶窦入路进行手术。3例患有视交叉受压的患者视力障碍迅速缓解。1例患者因病变复发导致复发性视交叉综合征,需要额外进行经颅切除包膜手术。不幸的是,术后一只眼睛的视力障碍仍然存在。内分泌随访显示所有病例的垂体功能未改变甚至恶化。我们的研究未发现一致的术前预测性发现。因此,我们认为所有患有视交叉综合征的患者都应进行减压手术,所有患有鞍内病变的患者都应进行诊断性手术。

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