Bettegowda Chetan, Adogwa Owoicho, Mehta Vivek, Chaichana Kaisorn L, Weingart Jon, Carson Benjamin S, Jallo George I, Ahn Edward S
Department of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
J Neurosurg Pediatr. 2012 Nov;10(5):398-405. doi: 10.3171/2012.8.PEDS12132. Epub 2012 Aug 31.
Choroid plexus tumors (CPTs) are rare intracranial neoplasms that constitute approximately 2%-5% of all pediatric brain tumors. Most of these tumors present with severe hydrocephalus. The optimal perioperative management and oncological care remain a matter of debate. The authors present the epidemiological and clinical features of CPTs from a 20-year single-institutional experience.
A total of 39 consecutive patients with pathologically proven CPTs (31 choroid plexus papillomas [CPPs] and 8 choroid plexus carcinomas [CPCs]) were included in this series. Patient demographics, clinical presentation, comorbidities, indications for surgery, radiological studies, tumor location, and all operative variables were reviewed for each case. Multivariate regression analysis was performed to identify independent predictors of tumor recurrence and survival.
The overall mean age (± SD) was 13.13 ± 19.59 years (15.27 ± 21.10 years in the CPP group and 3.66 ± 3.59 years in the CPC group). Hydrocephalus was noted at presentation in 34% of patients. The most common presenting symptoms were headache (32%) and nausea/vomiting (26%). Gross-total resection (GTR) was achieved in 86% of CPPs and in 71% of CPCs (p = 0.57). There was 100% survival in patients with CPPs observed at the 5- and 10-year follow-up and 71% survival in patients with CPCs at the 5-year follow-up. In a multivariate regression analysis, a diagnosis of papilloma, preoperative vision changes, or hydrocephalus; right ventricle tumor location; and GTR were all independently associated with a decreased likelihood of tumor recurrence at last follow-up.
The authors' study suggests that patients with CPCs are more likely to experience local recurrence and metastasis; hence, GTR with chemotherapy and radiotherapy, particularly for CPCs, is pivotal in preventing recurrence and prolonging survival. While GTR was important for local control following resection of CPPs, it had a minimal effect on prolonging survival in this patient cohort.
脉络丛肿瘤(CPTs)是罕见的颅内肿瘤,约占所有儿童脑肿瘤的2%-5%。这些肿瘤大多伴有严重脑积水。围手术期的最佳管理和肿瘤治疗仍存在争议。作者通过20年单机构经验介绍CPTs的流行病学和临床特征。
本系列纳入39例经病理证实的CPTs患者(31例脉络丛乳头状瘤[CPPs]和8例脉络丛癌[CPCs])。回顾了每例患者的人口统计学、临床表现、合并症、手术指征、影像学检查、肿瘤位置及所有手术变量。进行多因素回归分析以确定肿瘤复发和生存的独立预测因素。
总体平均年龄(±标准差)为13.13±19.59岁(CPP组为15.27±21.10岁,CPC组为3.66±3.59岁)。34%的患者初诊时发现脑积水。最常见的首发症状是头痛(32%)和恶心/呕吐(26%)。86%的CPPs和71%的CPCs实现了全切(GTR)(p = 0.57)。在5年和10年随访中,CPPs患者的生存率为100%,CPCs患者在5年随访中的生存率为71%。在多因素回归分析中,乳头状瘤诊断、术前视力改变或脑积水;右心室肿瘤位置;以及GTR均与末次随访时肿瘤复发可能性降低独立相关。
作者的研究表明,CPCs患者更易发生局部复发和转移;因此,GTR联合化疗和放疗,尤其是对CPCs患者,对于预防复发和延长生存期至关重要。虽然GTR对CPPs切除后的局部控制很重要,但对该患者队列的生存期延长影响极小。