期刊文献+

肉芽肿性垂体炎的诊断和治疗 被引量:3

Diagnosis and management of granulomatous hypophysitis
原文传递
导出
摘要 目的探讨肉芽肿性垂体炎的影像学特征及其诊断和治疗。方法回顾性分析7例肉芽肿性垂体炎的临床表现、影像学特征、诊断和治疗。结果7例肉芽肿性垂体炎术前误诊6例。临床表现主要为头痛、尿崩症、高泌乳素血症和垂体功能低下。影像学特征主要表现为鞍区病变沿增厚的垂体柄呈“舌状”向鞍上扩展。6例采用经鼻蝶窦入路,1例因术前诊断垂体脓肿而采用经额下入路手术治疗,术后口服激素替补治疗,多数症状缓解,影像学检查证实病灶明显缩小甚至消失。结论肉芽肿性垂体炎手术治疗可明确病理诊断,缓解症状,术后应口服激素替补治疗,定期随访。 Objective To investigate the diagnosis and management of granulomatous hypophysitis. Methods Seven patients with granulomatoushypophysitis were retrospectively analyzed with their signs and symptoms, radiological characteristics, diagnosis, and treatments. Results In the seven cases, six cases were misdiagnosed before operations. The clinical signs were headaches, diabetes inspidus, hyperprolactinemia, and hypopituitarism. Pituitary stalk thickening is a prominent image feature and is associated with the tongue - like extension of the sellar lesion into the suprasellar region. Surgery via the transsphenoidal route was performed on six cases and the transfrontal approach was chosen for one patient due to the additional diagnosis of onabscess preoperatively. Most of the patients had remission of clinical symptoms and signs after surgery with steroids and hormones replacement and lesions were reduced or even disappeared on MRI images. Conclusions Surgical intervention should be performed because it is difficult to make correct pathological diagnosis of granulomatous hypophysitis preoperatively and may improve symptoms and signs. Steroids and hormones replacement should be administrated after surgery and patients should be followed - up because of the natural course of the disorder.
出处 《中华神经外科杂志》 CSCD 北大核心 2013年第5期507-511,共5页 Chinese Journal of Neurosurgery
关键词 肉芽肿性垂体炎 尿崩症 高泌乳素血症 垂体功能低下 治疗 Granulomatous hypophysitis Diabetes inspidus Hyperprolactinemia Hypopituitarism Treatment
  • 相关文献

参考文献3

二级参考文献44

  • 1熊南翔,赵洪洋,赵甲山,朱贤立,林宁,林洪,张方成,林敏华.原发性垂体炎与垂体腺瘤的鉴别[J].中国误诊学杂志,2004,4(12):2017-2018. 被引量:4
  • 2吕朝晖,陆菊明,金文胜,窦京涛,母义明,潘长玉.淋巴细胞性垂体炎三例并文献复习[J].中华内科杂志,2005,44(6):446-449. 被引量:27
  • 3Honegger J, Fahlbusch R, Bornemann A, et al. Lymphocytic and granulomatous hypophysitis: experience with nine cases.Neurosurgery, 1997, 40: 713-722.
  • 4Buxton N, RobertsonI. Lymphocytic and granulocytic hypophysitis: a single centre experience. Br J Neurosurg, 2001,15: 242-245.
  • 5Beressi N, Beressi J, Cohen S, et al. Lymphocytic hypophysitis: A review of 145 cases. Ann Med Interne, 1999,150:327-341.
  • 6McGrail KM, Beyerl BD, Black PM, et al. Lymphocytic adenohypophysitis of pregnancy with complete recovery.Neurosurgery, 1987, 10:791-793.
  • 7Taylon C, Duff TA. Giant cell granuloma involving the pituitary gland: Case report. J Neurosurg,1980, 52:584-587.
  • 8Higuchi M, Arita N, Mori S, et al. Pituitary granuloma and chronic inflammatin of hypophysis: Clinical and immunohistochemical studies. Acta Neurochir(Wien) ,1993, 121:152-158.
  • 9Nussbaum CE, Okawara SH, Jacobs LS. lymphocytic hypophysitis with involvement of the cavernous sinus and hypothalamus.Neurosurgery, 1991, 28:440-444.
  • 10Ozawa Y, Shishiba OY. Recovery from lymphocytic hypophysitis associated with painful thyroiditis: clinical implications of circulating anti pituitary antibodies. Acta Endocrinol, 1993,28:493-498.

共引文献26

同被引文献62

引证文献3

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部