Zhao Heng, Cao Liangliang, Zhao Yang, Wang BaoCheng, Tian ShauiWei, Ma Jie
Department of Pediatric Neurosurgery, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.
Childs Nerv Syst. 2023 Mar;39(3):767-773. doi: 10.1007/s00381-022-05656-8. Epub 2022 Sep 6.
The aim of this study is to investigate the clinical characteristics and prognostic effects of different subtypes of suprasellar arachnoid cysts (SAC) in children.
Fifty patients with primary SAC who had undergone endoscopic treatment in our department between January 2010 and December 2020 were studied retrospectively. All patients underwent endoscopic treatment after diagnosis, including ventriculocystostomy (VC) in 23 cases and ventriculocystocisternostomy (VCC) in 27 cases. All patients were followed up regularly after the operation, including head computed tomography (CT)/magnetic resonance imaging (MRI), and Evans index (EI) and frontal and occipital horn ratio (FOHR) index were measured to assess changes in cyst volume and hydrocephalus. The prognosis was evaluated comprehensively on the data of the improvement of clinical symptoms, child growth and development correlation score, and reduction of cyst volume 12 months after surgery. According to the new classification of SAC, 50 cases of children were classified into three groups in which we compared the clinical characteristics of different subtypes of the three groups. Logistic regression was used to analyze the influencing factors of prognosis.
Completed success was achieved in 50 cases, including 31 cases with cyst volume reduction of more than 50% and 19 cases with cyst volume reduction of less than 50%. The median follow-up time was 55.3 months (22 ~ 113 months). According to the new classification criteria of SAC, there were 21 cases of SAC-1, 16 cases of SAC-2, and 13 cases of SAC-3. There were no statistically significant differences among the three groups in gender, birth weight, prenatal diagnosis, hydrocephalus, endocrine abnormalities, relief of postoperative symptoms, cyst wall texture, and surgical methods (P > 0.05). There was a statistically significant difference among the three groups in the change of the cyst volume and the maximum cyst diameter (P < 0.05), in which SAC-1 had the largest volume reduction, SAC-2 was more likely to cause endocrine symptoms and SAC-3 was inclined to lie in between. Multivariate logistic analysis showed that SAC classification and cyst wall texture were independent risk factors for the prognosis.
The clinical characteristics of different SAC subtypes are different, and SAC classification is one of the independent risk factors affecting prognosis.
本研究旨在探讨儿童鞍上蛛网膜囊肿(SAC)不同亚型的临床特征及预后影响。
回顾性研究2010年1月至2020年12月在我科接受内镜治疗的50例原发性SAC患儿。所有患者确诊后均接受内镜治疗,其中23例行脑室囊肿造瘘术(VC),27例行脑室囊肿脑池造瘘术(VCC)。术后对所有患者进行定期随访,包括头部计算机断层扫描(CT)/磁共振成像(MRI),并测量埃文斯指数(EI)和额枕角比(FOHR)指数以评估囊肿体积和脑积水的变化。根据术后12个月临床症状改善、儿童生长发育相关评分及囊肿体积缩小的数据综合评估预后。根据SAC的新分类,将50例患儿分为三组,比较三组不同亚型的临床特征。采用逻辑回归分析预后的影响因素。
50例均取得完全成功,其中囊肿体积缩小超过50%的有31例,囊肿体积缩小不足50%的有19例。中位随访时间为55.3个月(22~113个月)。根据SAC的新分类标准,SAC-1型21例,SAC-2型16例,SAC-3型13例。三组在性别、出生体重、产前诊断、脑积水、内分泌异常、术后症状缓解、囊肿壁质地及手术方式等方面差异均无统计学意义(P>0.05)。三组在囊肿体积变化和最大囊肿直径方面差异有统计学意义(P<0.05),其中SAC-1型体积缩小最大,SAC-2型更易引起内分泌症状,SAC-3型介于两者之间。多因素逻辑分析显示,SAC分类和囊肿壁质地是预后的独立危险因素。
不同SAC亚型的临床特征不同,SAC分类是影响预后的独立危险因素之一。