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A retrospective study of children with neuroblastoma at our tertiary centre with varied pattern of presentation, protocol based management and outcome in these kids

机译:在我们的三级中心对神经母细胞瘤患儿进行回顾性研究,研究结果显示这些患儿的表现形式,基于方案的管理方式和结果各异

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:Neuroblastoma is a neuroendocrine tumor arising from theneural crest of the sympathetic nervous system.It is the most commonextracranial solid tumor of childhood, which is often localized in theretroperitoneal space, mainly in the adrenal glands, paravertebral retro-peritoneal space, at rare in the posterior mediastinum,in neck,presacralarea.It has a diverse clinical presentation and course depending on thetumour biology.First symptoms of neuroblastoma are nonspecific,mimicvarious diseases.Clinical manifestations depend on the localization of thetumor,stage presence and location of metastases.Unique features of thesetumours are the early age of onset,the high frequency of metastatic diseaseat diagnosis and the tendency for spontaneous regression of tumours ininfancy.Most malignant tumours have amplification of the MYCN onco-gene which is usually associated with poor outcome,even in localizeddisease.
机译:神经母细胞瘤是由交感神经系统神经c引起的神经内分泌肿瘤,是儿童时期最常见的颅外实体瘤,通常位于腹膜后腹间隙,主要分布在肾上腺,椎旁腹膜后间隙,罕见。后部纵隔位于颈部,前。骨。根据肿瘤生物学的不同,其临床表现和病程也不同。神经母细胞瘤的首发症状是非特异性,微小疾病。临床表现取决于肿瘤的位置,分期和转移的位置。这些肿瘤是发病年龄的早期,诊断时转移性疾病的高发率以及婴儿期肿瘤的自发消退的趋势。大多数恶性肿瘤的MYCN癌基因扩增现象通常与不良预后相关,甚至在局部疾病中也是如此。

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