Department of Neurosurgery, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Neurosurg Focus. 2010 Oct;29(4):E5. doi: 10.3171/2010.7.FOCUS10153.
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.
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 μg/l, and a random GH value of less than 2.5 μg/l were required to establish biochemical cure postoperatively.
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.
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.
作者使用严格的生化缓解标准评估了经内镜经蝶窦切除生长激素(GH)分泌性垂体腺瘤的手术结果,并确定了术前显著影响缓解率的因素。
对前瞻性维护的数据库进行回顾性分析。作者回顾了经内镜切除 GH 分泌性垂体腺瘤的病例。该队列包括 26 例患者,随访时间为 3-60 个月(平均 24.5 个月)。术后生化治愈的标准为年龄适当的、正常化的胰岛素样生长因子-I 浓度、口服葡萄糖负荷后 GH 水平低于 1.0μg/l 的最低点和随机 GH 值低于 2.5μg/l。
总的来说,在 57.7%接受单纯经蝶窦垂体腺瘤切除术治疗肢端肥大症的患者中,达到了内分泌学治愈。平均临床随访时间为 24.5 个月。微腺瘤(4 例)患者的治愈率为 75%,而大腺瘤(22 例)患者的治愈率为 54.5%。海绵窦侵袭(Knosp 分级 3 级和 4 级)与缓解率显著降低相关(p = 0.0068)。Hardy 分级 3 级和 4 级肿瘤也不太可能实现生化治愈(p = 0.013)。总的并发症发生率为 11.5%,包括 2 例短暂性尿崩症和 1 例术后脑脊液漏,均非手术治疗。
与传统的显微外科技术相比,经内镜经蝶窦入路治疗非侵袭性大腺瘤的 GH 分泌性垂体腺瘤的结果相似。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。