Daszkiewicz Paweł, Maryniak Agnieszka, Roszkowski Marcin, Barszcz Sławomir
Department of Neurosurgery, Children's Memorial Health Institute, Al. Dzieci Polskich 20, PL-04-730, Warsaw, Poland.
Childs Nerv Syst. 2009 Jul;25(7):855-60. doi: 10.1007/s00381-009-0855-1. Epub 2009 May 6.
Increasing incidence of pediatric brain tumors and improving survival rates encouraged us to assess long-term functional outcome of patients with cerebellar juvenile pilocytic astrocytoma (JPA).
Our study encompassed 105 children treated since 1980-2005 and consisted in analysis of mailed, custom-designed questionnaires.
Mean follow-up time was 8.3 years. Sixty out of 104 patients presented permanent neurological deficits and 47/104 presented significant behavioral disorders. Eighty-nine children continued their education at primary, secondary or high school level. Most patients and their parents were satisfied with treatment outcome. Patients' and parents' notes were usually concordant.
Long-term functional treatment outcome of cerebellar JPA is relatively favorable, in spite of permanent neurological deficits and emotional disorders in over half of the patients. Vermian tumors are associated with worse long-term functional outcome. Neurological deficits and emotional disorders do not preclude further education and independent functioning.
小儿脑肿瘤发病率的上升以及生存率的提高促使我们评估小脑青少年毛细胞型星形细胞瘤(JPA)患者的长期功能预后。
我们的研究纳入了1980年至2005年期间接受治疗的105名儿童,并对邮寄的定制问卷进行了分析。
平均随访时间为8.3年。104名患者中有60名存在永久性神经功能缺损,104名中有47名存在明显的行为障碍。89名儿童继续接受小学、中学或高中教育。大多数患者及其父母对治疗结果满意。患者和父母的记录通常一致。
尽管超过半数的患者存在永久性神经功能缺损和情绪障碍,但小脑JPA的长期功能治疗结果相对良好。蚓部肿瘤与较差的长期功能预后相关。神经功能缺损和情绪障碍并不妨碍进一步接受教育和独立生活。