Department of Neurosurgery, University of Erlangen-Nuremberg, Erlangen, Germany.
J Neurosurg. 2012 Feb;116(2):373-84. doi: 10.3171/2011.6.JNS081451. Epub 2011 Sep 23.
The authors report surgical and endocrinological results of a series of 73 cases of craniopharyngioma that they treated surgically since 1997 to demonstrate their change in treatment strategy and its effect on outcome compared with a previous series and results reported in the literature.
A total of 73 patients underwent surgery for craniopharyngiomas between May 1997 and January 2005. In patients with poor clinical or neuropsychological condition, even following pretreatment, only stereotactic cyst aspiration took place (8 cases). In the remaining patients, gross-total resection (GTR) was intended and appeared to be possible. The most frequent approaches were subfrontal (27 cases) and transsphenoidal (26 cases); in some cases, a multistep approach was used. The rate of GTR, complications, and functional outcome (comparing pre- and postoperative endocrine and neuropsychological testing) were evaluated. The mean duration of follow-up was 25.2 months.
Gross-total resection was achieved in 88.5% of cases in which a transsphenoidal approach was used and 79.5% of those in which a transcranial approach was used (85.2% of those in which a subfrontal approach was used and 72.7% of those in which a frontolateral approach was used). In the total series, GTR was achieved in 83.1% of cases (vs 49.3% in the authors' former series). The complication rate was 13.8% without any mortality. New endocrine deficits were observed more frequently in patients treated with transcranial approaches over the years (16.3%-66.7% vs 2.6%-50.0%) but were less frequent after transsphenoidal approaches (5.2%-19.2% vs 2.9%-45.7%).
Open surgery with intended total resection remains the treatment of choice in most patients. Initial stereotactic cyst aspiration or medical pretreatment to improve the patients' condition and adequate choice of surgical approach(es) are essential to achieve that goal. Nevertheless, a moderate increase in endocrinological deficits has to be accepted. The authors recommend using radiotherapy only in cases in which there are tumor remnants or disease progression after surgery.
作者报告了自 1997 年以来对 73 例颅咽管瘤患者进行的一系列手术和内分泌学结果,以展示他们的治疗策略变化及其与之前的系列研究和文献报道结果的比较。
1997 年 5 月至 2005 年 1 月期间,73 例患者接受颅咽管瘤手术治疗。对于临床或神经心理学状况较差的患者,即使经过预处理,仅行立体定向囊肿抽吸术(8 例)。对于其余患者,计划进行大体全切除(GTR),且手术似乎可行。最常见的入路是额下入路(27 例)和经蝶窦入路(26 例);在某些情况下,采用多步入路。评估 GTR 率、并发症和功能结局(比较术前和术后内分泌和神经心理学测试)。平均随访时间为 25.2 个月。
经蝶窦入路使用时,GTR 达到 88.5%;经颅入路使用时,GTR 达到 79.5%(额下入路时,GTR 达到 85.2%,经眶颧入路时,GTR 达到 72.7%)。在总系列中,GTR 达到 83.1%(与作者之前的系列研究中的 49.3%相比)。并发症发生率为 13.8%,无死亡病例。随着时间的推移,经颅入路治疗的患者中,新出现内分泌缺陷更为常见(16.3%-66.7%比 2.6%-50.0%),但经蝶窦入路治疗的患者中较少见(5.2%-19.2%比 2.9%-45.7%)。
开放性手术并进行预期的全切仍然是大多数患者的治疗选择。初始立体定向囊肿抽吸术或药物预处理以改善患者病情,并适当选择手术入路,对于实现这一目标至关重要。然而,必须接受适度增加内分泌缺陷的风险。作者建议仅在术后存在肿瘤残留或疾病进展的情况下使用放疗。