Munjal Satyashiva, Chatterjee Uttara, Vinchon Matthieu, Chatterjee Sandip
Department of Neurosurgery, Park Clinic, 4, Gorky Terrace, Kolkata, 700017, West Bengal, India.
Department of Pathology, IPGME&R, Kolkata, India.
Childs Nerv Syst. 2016 Sep;32(9):1633-40. doi: 10.1007/s00381-016-3135-x. Epub 2016 Jun 14.
Infantile brain tumours (age < 1 year) are increasingly being diagnosed due to advances in prenatal and perinatal diagnostic imaging. We present here our retrospective study of 64 infant brain tumours that brings to the fore the epidemiology, clinical presentation, pathology and outcome of this unique subset of paediatric brain tumours presenting to two tertiary referral centres in Kolkata in India and Lille in France between the years 1999 and 2014.
Data was retrospectively collected from Kolkata (n = 30) and Lille (n = 34) for patients presenting with infant brain tumours and analysed for factors such as age at presentation, clinical features, gender, location of tumour, pathology, management and outcome. Follow-up was available for all patients.
Mean age at presentation was 6.8 months at Kolkata and 6.3 months at Lille. More than two-thirds of tumours in both the groups were supratentorial and presented with signs of raised intracranial pressure. There was also a similar proportion of tumours presenting as congenital tumours. At Kolkata, germ cell tumours (n = 7) were the most common while low-grade gliomas (n = 11) formed the largest group at Lille. Kolkata had a higher incidence of high-grade gliomas (n = 5) and PNETs (n = 4) while ATRT (n = 3) and choroid plexus carcinoma (n = 4) were more common at Lille. Surgery was the mainstay of treatment at both centres.
Brain tumours in infants presenting to tertiary centres in Europe and India are challenging to manage and usually have dismal prognosis. These tumours differ markedly in the pathology and, therefore, overall outcome. Surgery forms mainstay of treatment. Radiotherapy is best avoided in this age group.
由于产前和围产期诊断成像技术的进步,婴儿脑肿瘤(年龄<1岁)的诊断越来越多。我们在此展示对64例婴儿脑肿瘤的回顾性研究,该研究揭示了1999年至2014年间在印度加尔各答和法国里尔的两个三级转诊中心就诊的这一独特儿科脑肿瘤亚组的流行病学、临床表现、病理学和预后情况。
回顾性收集加尔各答(n = 30)和里尔(n = 34)患有婴儿脑肿瘤患者的数据,并分析诸如就诊年龄、临床特征、性别、肿瘤位置、病理学、治疗和预后等因素。所有患者均有随访数据。
加尔各答患者的平均就诊年龄为6.8个月,里尔为6.3个月。两组中超过三分之二的肿瘤位于幕上,并伴有颅内压升高的体征。先天性肿瘤的比例也相似。在加尔各答,生殖细胞肿瘤(n = 7)最为常见,而在里尔,低级别胶质瘤(n = 11)是最大的一组。加尔各答高级别胶质瘤(n = 5)和原始神经外胚层肿瘤(PNETs,n = 4)的发病率较高,而在里尔,非典型畸胎样/横纹肌样肿瘤(ATRT,n = 3)和脉络丛癌(n = 4)更为常见。手术是两个中心的主要治疗方法。
在欧洲和印度的三级中心就诊的婴儿脑肿瘤治疗具有挑战性且预后通常不佳。这些肿瘤在病理学上有显著差异,因此总体预后也不同。手术是主要治疗方法。该年龄组最好避免放疗。