首页> 外文期刊>Neurosurgical focus >Outcomes after a purely endoscopic transsphenoidal resection of growth hormone-secreting pituitary adenomas
【24h】

Outcomes after a purely endoscopic transsphenoidal resection of growth hormone-secreting pituitary adenomas

机译:单纯内镜下经蝶窦切除生长激素分泌性垂体腺瘤的结果

获取原文
获取原文并翻译 | 示例
           

摘要

Object. Using strict biochemical remission criteria, the authors assessed surgical outcomes after endoscopic transsphenoidal resection of growth hormone (GH)-secreting pituitary adenomas and identified preoperative factors that significantly influence the rate of remission.Methods. A retrospective review of a prospectively maintained database was performed. The authors reviewed cases in which an endoscopic resection of GH-secreting pituitary adenomas was performed. The cohort consisted of 26 patients who had been followed for 3-60 months (mean 24.5 months). The thresholds of an age-appropriate, normalized insulin-like growth factor-I concentration, a nadir GH level after oral glucose load of less than 1.0 mug/1, and a random GH value of less than 2.5 mug/1 were required to establish biochemical cure postoperatively.Results. Overall, in 57.7% of patients undergoing a purely endoscopic transsphenoidal pituitary adenectomy for acromegaly, an endocrinological cure was achieved. The mean clinical follow-up duration was 24.5 months. In patients with microadenomas (4 cases) the cure rate was 75%, whereas in patients harboring macroadenomas (22 cases) the cure rate was 54.5%. Cavernous sinus invasion (Knosp Grades 3 and 4) was associated with a significantly lower remission rate (p = 0.0068). Hardy Grade 3 and 4 tumors were also less likely to achieve biochemical cure (p = 0.013). The overall complication rate was 11.5% including 2 incidents of transient diabetes insipidus and 1 postoperative CSF leak, which were treated nonoperatively.Conclusions. A purely endoscopic transsphenoidal approach to GH-secreting pituitary adenomas leads to similar outcome for noninvasive macroadenomas compared with traditional microsurgical techniques. Furthermore, this approach may often provide maximal visualization of the tumor, the pituitary gland, and the surrounding neurovascular structures.
机译:目的。使用严格的生化缓解标准,作者评估了经内镜经蝶窦切除的分泌生长激素(GH)的垂体腺瘤的手术效果,并确定了明显影响缓解率的术前因素。回顾性审查了前瞻性维护的数据库。作者回顾了在内窥镜下切除分泌GH的垂体腺瘤的病例。该队列包括26例患者,随访时间为3-60个月(平均24.5个月)。建立适合年龄的标准胰岛素样生长因子-I浓度的阈值,口服葡萄糖负荷后的最低GH水平低于1.0杯/ 1,随机GH值应低于2.5杯/ 1。术后生化治愈。总体而言,在接受纯内镜下经蝶窦垂体腺切除术治疗肢端肥大症的患者中,有57.7%的患者获得了内分泌治疗。平均临床随访时间为24.5个月。有微腺瘤的患者(4例)治愈率为75%,而有大腺瘤的患者(22例)治愈率为54.5%。海绵窦浸润(诺氏3级和4级)与缓解率显着降低有关(p = 0.0068)。 Hardy 3级和4级肿瘤也不太可能实现生化治愈(p = 0.013)。总体并发症发生率为11.5%,包括2例短暂性尿崩症和1例术后脑脊液漏,这些均未经手术治疗。与传统的显微外科手术技术相比,单纯的内窥镜经蝶窦入路生长激素分泌性垂体腺瘤可导致无创大腺瘤的相似结果。此外,这种方法通常可以提供肿瘤,垂体和周围神经血管结构的最大可视化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号