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巨大垂体腺瘤的外科治疗:95例连续患者的治疗策略与结果

Surgical treatment of giant pituitary adenomas: strategies and results in a series of 95 consecutive patients.

作者信息

Mortini Pietro, Barzaghi Raffaella, Losa Marco, Boari Nicola, Giovanelli Massimo

机构信息

Department of Neurosurgery, University of Brescia, Brescia, Italy.

出版信息

Neurosurgery. 2007 Jun;60(6):993-1002; discussion 1003-4. doi: 10.1227/01.NEU.0000255459.14764.BA.

Abstract

OBJECTIVE

Giant pituitary adenomas, defined as those measuring at least 4 cm in maximum diameter, are a therapeutic challenge. We report our experience in a large, consecutive series of patients with giant adenomas.

METHODS

Between 1990 and 2004, 95 patients with a giant pituitary adenomas underwent surgery at our department. Nonfunctioning pituitary adenoma was the most frequent type (n = 70; 73.7%), whereas hormone-secreting adenomas numbered only 25 (26.3%). The mean age at the time of surgery (+/-standard error of the mean) was 48.4 +/- 1.5 years; there were 66 men (69.5%) and 29 women (20.5%).

RESULTS

In total, 111 surgical procedures were performed. Of these, 85 approaches (76.6%) were transsphenoidal and 26 (23.4%) were transcranial. Visual improvement occurred in 59 of the 79 patients with preoperative defect who could be evaluated after surgery (74.7%). Radical tumor excision was obtained in 14 patients (14.7%). Adjuvant medical and radiation therapies led to 74.5% (95% confidence interval, 62.7-86.4%) control of tumor growth at 5 years. This was not different in patients with nonfunctioning pituitary adenomas compared with patients with hormone-secreting tumors. In the subgroup of patients with nonfunctioning pituitary adenomas, radiation therapy had a protective role against tumor growth (P < 0.01).

CONCLUSION

Maximal surgical removal of giant adenomas through the transsphenoidal or transcranial approach, or both, aimed to relieve compression of the optic pathway and reduce tumor volume as much as possible, offers the best chances to control the tumor when followed with adjuvant medical and radiation therapies.

摘要

目的

巨大垂体腺瘤定义为最大直径至少4厘米的垂体腺瘤,是一种治疗挑战。我们报告了我们在一大组连续的巨大腺瘤患者中的经验。

方法

1990年至2004年期间,95例巨大垂体腺瘤患者在我科接受了手术。无功能垂体腺瘤是最常见的类型(n = 70;73.7%),而分泌激素的腺瘤仅25例(26.3%)。手术时的平均年龄(±平均标准误差)为48.4±1.5岁;男性66例(69.5%),女性29例(20.5%)。

结果

共进行了111次手术。其中,85例(76.6%)采用经蝶窦入路,26例(23.4%)采用经颅入路。79例术前有视力缺陷且术后可评估的患者中,59例(74.7%)视力得到改善。14例患者(14.7%)实现了肿瘤根治性切除。辅助药物和放射治疗使5年时肿瘤生长控制率达到74.5%(95%置信区间,62.7 - 86.4%)。无功能垂体腺瘤患者与分泌激素肿瘤患者相比,这一结果无差异。在无功能垂体腺瘤患者亚组中,放射治疗对肿瘤生长有保护作用(P < 0.01)。

结论

通过经蝶窦或经颅入路或两者结合,最大程度地手术切除巨大腺瘤,旨在缓解视路压迫并尽可能减少肿瘤体积,在辅助药物和放射治疗的情况下,为控制肿瘤提供了最佳机会。

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