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原发性垂体炎:16例单中心经验

Primary hypophysitis: a single-center experience in 16 cases.

作者信息

Leung Gilberto K K, Lopes Maria-Beatriz S, Thorner Michael O, Vance Mary Lee, Laws Edward R

机构信息

Department of Neurological Surgery, University of Virginia Health System, Charlottesville, Virginia 22908, USA.

出版信息

J Neurosurg. 2004 Aug;101(2):262-71. doi: 10.3171/jns.2004.101.2.0262.

Abstract

OBJECT

The authors review their experience in the treatment of 16 patients with primary hypophysitis.

METHODS

A retrospective study was undertaken to review cases of primary hypophysitis. The mean age of the patients was 47 years and there was an equal distribution of sexes. Recent pregnancy and underlying autoimmunity were noted in 50% of the patients. Two patients had undergone previous transsphenoidal operations at other centers, one for prolactinoma and another for hypophysitis. Headache, anterior pituitary deficiency, and suprasellar mass lesions were the most common presenting features. The initial presumptive diagnosis was pituitary adenoma in six patients (37.5%) and inflammatory hypophysitis in 10 (62.5%). Five patients received initial medical therapy for hypophysitis; although three (60%) responded satisfactorily, two (40%) did not and later underwent surgery. Altogether 13 patients (81.2%) underwent transsphenoidal surgery. The histological diagnoses were lymphocytic hypophysitis in 10 (76.9%) and granulomatous hypophysitis in three (23.1%) of the surgically treated patients. A coexistent Rathke cleft cyst was noted in one patient. There was no death in this series. One patient experienced postoperative cerebrospinal fluid leakage and meningitis. One patient had bilateral internal carotid artery occlusion secondary to inflammatory involvement of the cavernous sinuses and arteritis. This patient recovered and is capable of independent functional activities.

CONCLUSIONS

All surgical patients experienced improvement in their headache and/or visual field defects and none had visual deterioration. None of the patients experienced any improvement in endocrine function and all required long-term hormone replacement. Transsphenoidal surgery was a safe and effective treatment especially for visual and pressure symptoms. A postoperative recurrence developed in two patients (15.4%) and the treatment modalities included steroid therapy, repeated surgery, and radiosurgery.

摘要

目的

作者回顾了他们治疗16例原发性垂体炎患者的经验。

方法

进行一项回顾性研究以复查原发性垂体炎病例。患者的平均年龄为47岁,男女分布均等。50%的患者有近期妊娠及潜在自身免疫性疾病史。两名患者曾在其他中心接受过经蝶窦手术,其中一名因催乳素瘤,另一名因垂体炎。头痛、垂体前叶功能减退及鞍上肿块病变是最常见的临床表现。最初的初步诊断为6例(37.5%)垂体腺瘤和10例(62.5%)炎症性垂体炎。5例患者最初接受了垂体炎的药物治疗;尽管3例(60%)反应良好,但2例(40%)效果不佳,随后接受了手术。共有13例患者(81.2%)接受了经蝶窦手术。手术治疗患者的组织学诊断为淋巴细胞性垂体炎10例(76.9%),肉芽肿性垂体炎3例(23.1%)。1例患者并存拉克囊肿。本系列无死亡病例。1例患者术后出现脑脊液漏和脑膜炎。1例患者因海绵窦炎症累及和动脉炎继发双侧颈内动脉闭塞。该患者康复,能够独立进行功能活动。

结论

所有接受手术的患者头痛和/或视野缺损均有改善,无一例视力恶化。所有患者内分泌功能均无改善,均需长期激素替代治疗。经蝶窦手术是一种安全有效的治疗方法,尤其适用于视觉和压迫症状。2例患者(15.4%)术后复发,治疗方式包括类固醇治疗、再次手术和放射外科治疗。

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