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颅咽管瘤患儿起源部位和肿瘤生长速度对临床结局的影响。

The impact of the site of origin and rate of tumour growth on clinical outcome in children with craniopharyngiomas.

机构信息

Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

Clin Endocrinol (Oxf). 2012 Jan;76(1):103-10. doi: 10.1111/j.1365-2265.2011.04172.x.

Abstract

OBJECTIVES

Data on many predictors of hypothalamic-pituitary axis dysfunction associated with childhood craniopharyngioma (CP) are rather inconsistent, probably reflecting the variable but as yet unclarified growth pattern of these tumours. The aim of this study was to define the determinative role of tumour growth pattern on hypothalamic-pituitary axis function and outcomes for childhood CPs.

PATIENTS AND METHODS

The authors retrospectively analysed the records of 81 consecutive children with primary CP who underwent a uniform treatment paradigm of attempted radical resection performed by a single surgeon. The patients were divided into two subgroups based on tumour location and growth patterns: group A (infra-diaphragmatic sellar tumours: 34 cases) and group B [third ventricular floor (3rd VF) tumours: 47 cases]. The children's pre- and postsurgical endocrinological and hypothalamic disturbances were compared. Pituitary function and hypothalamic statues were quantitatively assessed using classification systems proposed in the previous studies.

RESULTS

Preoperative pituitary function was more severely compromised in patients in group A than those in group B and deteriorated significantly following resection in both groups. (Average pituitary function scores increased from 2·19 ± 0·83 to 3·31 ± 0·74, P < 0·001). At the last follow-up, children with 3rd VF tumours had more prevalent weight gain (median body mass index: 23·1 kg/m(2) in group B vs 19·7 kg/m(2) in group A, P < 0·001) and increased hypothalamic dysfunction (average hypothalamic status scores: 2·04 ± 0·97 in group B vs 1·29 ± 0·57 in group A, P < 0·001). Children with 3rd VF tumours had a significantly lower probability of recurrence-free survival than those with sellar tumours (at 5 years: 74%vs 49%, respectively; at 10 years: 66%vs 32%, respectively; P = 0·02).

CONCLUSIONS

Substantial differences in the outcome of childhood CP with different tumour growth patterns and locations were found, which suggested that diverse therapeutic considerations, especially endocrinological substitution, might be emphasized.

摘要

目的

与儿童颅咽管瘤(CP)相关的下丘脑-垂体轴功能障碍的许多预测因素的数据相当不一致,这可能反映了这些肿瘤的可变但尚未阐明的生长模式。本研究的目的是确定肿瘤生长模式对儿童 CP 下丘脑-垂体轴功能和结局的决定性作用。

患者和方法

作者回顾性分析了 81 例连续接受单一外科医生行根治性切除术的原发性 CP 儿童患者的记录。根据肿瘤位置和生长模式将患者分为两组:A 组(膈下鞍内肿瘤:34 例)和 B 组(第三脑室底肿瘤:47 例)。比较了儿童术前和术后的内分泌和下丘脑紊乱情况。使用以前研究中提出的分类系统定量评估垂体功能和下丘脑状态。

结果

A 组患者的术前垂体功能较 B 组严重受损,两组患者术后均显著恶化。(平均垂体功能评分从 2.19 ± 0.83 增加到 3.31 ± 0.74,P < 0.001)。在最后一次随访时,3 脑室底肿瘤患儿的体重增加更为常见(B 组的中位数体重指数为 23.1 kg/m²,A 组为 19.7 kg/m²,P < 0.001),且下丘脑功能障碍增加(B 组平均下丘脑状态评分 2.04 ± 0.97,A 组 1.29 ± 0.57,P < 0.001)。与鞍内肿瘤相比,3 脑室底肿瘤患儿无复发生存率显著降低(5 年时分别为 74%和 49%,10 年时分别为 66%和 32%,P = 0.02)。

结论

发现具有不同肿瘤生长模式和位置的儿童 CP 的结果存在显著差异,这表明可能需要强调不同的治疗考虑因素,特别是内分泌替代治疗。

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