Follow up of Medulloblastoma’s Treatment Retrospective Study of 144 Cases

K. Badache, N. Habchi, F.Z Bendib, K. Khalfi, N. Ioualalen, Et M. Djaafer
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Abstract

Introduction: Medulloblastoma is the most common childhood primary CNS tumor, and treatment approaches have evolved over the past three decades. Despite recent improvements in cure rates, prediction of disease outcome remains a major challenge and survivors suffer from serious therapy-related side-effects. Patients and Methods: A retrospective study including 144 patients with medulloblastoma were performed at the Neurosurgery Department in Ait IDDIR Health Hospital Establishment between The period of January 2004 and December 2014. In each case, diagnosis was made clinically and confirmed radiologically and histo-pathologically. All patients were operated and received the adjuvant treatment Results and discussion: Out of 144 patients, 63 (44%) patients were females and 81 (56%) were males. We have 59 cases who had age ranged from 05 months to 5 years, however, we had 85 cases who had more than 5 years; we identified 29 (58%) children and 21 (42%) adults. Clinical manifestations of meduloblastoma vary widely according to the location. The vermis is the main location of the child with 95%. The most frequent clinical manifestations found were Intracranial hypertension syndrome and static and kinetic cerebellar syndrome, 98% patients had intracranial hypertension at diagnosis: 1,4% with engagement (2 cases) and 0,7% with coma(01 case). A ventriculo-peritoneal shunt was performed in all patients, 01 case after surgical removal. The most common complications were as follows: Meningitis ( 0,2%),ventriculitis (0,2%), CSF leakage (0,4%), post-surgical hematoma (0,2%), Shunt dysfunction ( 0,6%), aggravation of the cerebellar syndrom (0,4%), affection of mixed nerves ( 0,2%) and cerebellar mutism (0,4%). Tumor architecture was classified as classic (Grade II) and desmoplasic. We had T2M0 in 41(28,47%) cases, T2M2 in 2 (1,38%)cases ,T3aM0 in 98(68%)cases,T3bM3 in 2(1,38%) cases and T3bM4 in 1 (0,7%)case. During follow-up period, recurrence occurred in 15 (10%) cases, sustentorial metastasis in 04 (2,7%) cases, leptomeningeal dissemination in 03 (2%) cases and medullary metastasis in 03 (2%) cases. The five years survival rate was 84%. Conclusion: the surgical treatment of medulloblastoma remains a difficult therapeutic challenge because they have the most virulent form of the disease and are at highest risk for treatment-related sequelae.
髓母细胞瘤144例治疗随访回顾性研究
简介:髓母细胞瘤是最常见的儿童原发性中枢神经系统肿瘤,治疗方法在过去三十年中不断发展。尽管最近治愈率有所提高,但预测疾病结果仍然是一个重大挑战,幸存者会遭受严重的治疗相关副作用。患者和方法:2004年1月至2014年12月,在Ait IDDIR健康医院的神经外科对144名髓母细胞瘤患者进行了回顾性研究。在每个病例中,都进行了临床诊断,并经放射学和组织病理学证实。结果与讨论:144例患者中,女性63例(44%),男性81例(56%)。我们有59例年龄在05个月到5岁之间,然而,我们有85例年龄超过5岁 年;我们确定了29名(58%)儿童和21名(42%)成年人。髓母细胞瘤的临床表现因部位而异。蠕虫是儿童的主要部位,占95%。最常见的临床表现是颅内高压综合征和静态和动态小脑综合征,98%的患者在诊断时患有颅内高压:1,4%的患者参与(2例),0,7%的患者昏迷(01例)。所有患者均进行了脑室-腹膜分流术,其中01例在手术切除后进行。最常见的并发症有:脑膜炎(0.2%)、脑室炎(0.2%),脑脊液漏(0.4%),术后血肿(0.2%);分流功能障碍(0.6%);小脑综合征加重(0.4%);混合神经病变(0.2%)和小脑缄默症(0.4%)。肿瘤结构分为经典型(II级)和结缔组织增生型。T2M0 41例(28,47%),T2M2 2例(1.38%),T3aM0 98例(68%),T3bM3 2例(1,38%)和T3bM4 1例(0.7%)。随访期间,复发15例(10%),持续转移04例(2.7%),软脑膜播散03例(2%),髓质转移03例(3%)。五年生存率为84%。结论:髓母细胞瘤的手术治疗仍然是一个困难的治疗挑战,因为它们是该疾病中毒性最强的一种,并且产生治疗相关后遗症的风险最高。
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