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Incidental findings of mass lesions on neuroimages in children

机译:儿童神经影像上大量病变的偶然发现

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Increasing use of neuroimaging in children has led to more incidental findings of CNS mass lesions, the management of which is uncertain. The authors' aims in this study are to describe these mass lesions and their evolution, as well as to discuss the management options and determine the prevalence of incidental CNS mass lesions at their pediatric clinic. A retrospective study was undertaken in children with primary CNS tumors who were younger than 18 years old and were admitted to the University Children's Hospital of Zurich, Switzerland, between January 1995 and December 2010. In 19 (5.7%) of 335 patients with newly diagnosed CNS tumors, the diagnosis of a CNS mass lesion was an incidental finding. Reasons for obtaining neuroimages in these 19 patients were head trauma (in 6 patients); research protocols (in 3); nasal/orbital malformations (in 2); endocrinological and psychiatric evaluations (in 2); and vertebral bone anomaly without neurological signs, absence seizures, congenital ataxia, recurrent vomiting, developmental delay, and “check-up” at the explicit request of the parents (in 1 patient each). Seven patients underwent immediate surgery for low-grade glioma (4 patients) and craniopharyngioma, ependymoma, and choroid plexus papilloma (1 patient each); and 12 were treated conservatively or were observed. Ten of 12 conservatively treated patients remained stable (median follow-up time 1.8 years) and the other 2 underwent delayed surgery because of tumor progression (medulloblastoma in one patient and fibrillary astrocytoma in the other). Clinicians are increasingly challenged by the discovery of incidental CNS mass lesions. A subgroup of such lesions (with typical imaging patterns such as tectal glioma and dysembryoplastic neuroepithelial tumor) can be monitored conservatively, clinically, and radiographically. Future prospective studies are needed to define optimal management strategies based on larger collections of natural histories, as well as to assess the true prevalence of incidental CNS mass lesions.
机译:儿童中越来越多地使用神经影像技术导致了更多的中枢神经系统块状病变的偶然发现,其治疗尚不确定。作者在本研究中的目的是描述这些块状病变及其演变,并讨论治疗方案并确定其儿科临床中偶然发生的CNS块状病变的患病率。 1995年1月至2010年12月间,对瑞士苏黎世大学儿童医院收治的18岁以下未患有中枢神经系统肿瘤的儿童进行了回顾性研究。在335例新诊断的患者中,有19例(5.7%)中枢神经系统肿瘤,中枢神经系统肿块病变的诊断是偶然发现。在这19例患者中获得神经影像的原因是头部创伤(在6例患者中);研究方案(3);鼻/眼眶畸形(2);内分泌和精神病学评估(2);和椎骨异常,无神经系统症状,无癫痫发作,先天性共济失调,反复呕吐,发育迟缓和应父母明确要求进行“检查”(每人1名患者)。 7例因低度神经胶质瘤(4例),颅咽管瘤,室间隔膜瘤和脉络丛乳头状瘤(各1例)立即接受手术;和12个被保守治疗或被观察到。 12例接受保守治疗的患者中有10例保持稳定(中位随访时间为1.8年),另外2例由于肿瘤进展而延迟手术(一名患者为髓母细胞瘤,另一例为纤维状星形细胞瘤)。发现偶然的中枢神经系统大块病变,临床医生正面临越来越多的挑战。可以通过保守,临床和影像学检查来监测此类病变的亚组(具有典型的成像模式,例如顶盖神经胶质瘤和发育不良的神经上皮肿瘤)。需要进行未来的前瞻性研究,以根据大量的自然历史记录确定最佳的治疗策略,并评估偶然发生的中枢神经系统块状病变的真实发生率。

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