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首页> 外文期刊>Journal of neurosurgery. Pediatrics. >Hemorrhagic presentations of cerebellar pilocytic astrocytomas in children resulting in death: report of 2 cases
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Hemorrhagic presentations of cerebellar pilocytic astrocytomas in children resulting in death: report of 2 cases

机译:儿童小脑毛细胞星形细胞瘤出血导致死亡:2例报告

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Acute hemorrhagic presentation in pilocytic astrocytomas (PAs) has become increasingly recognized. This type of presentation poses a clinically emergent situation in those hemorrhages arising in PAs of the cerebellum, the most frequent site, because of the limited capacity of the posterior fossa to compensate for mass effect, predisposing to rapid neurological deterioration. As examples, we describe two cases of fatal hemorrhagic cerebellar PAs: one of a child with a slowly growing stereotypical WHO Grade I PA with a 1-year period of symptomatology that preceded a rapid clinical deterioration, and another of an asymptomatic child having a PA variant, presenting with progressive obtundation following a presumed Valsalva event. These two scenarios parallel previous reports in the literature of either a setting of progressive expression of cerebellar dysfunction and transient episodes of raised intracranial pressure (ICP), or abrupt onset of features of increased ICP in a previously well child. The literature is further reviewed for a current understanding of the factors that predispose, initiate and propagate bleeding, with specific reference to the role of vascular endothelial growth factor and other angiogenic agents in the genesis and stability of the vasculature in PAs. In this context, we propose that obliterative vascular mural hyalinization with associated altered flow dynamics and microaneurysm formation was the pathogenesis of the hemorrhage in our first case. In the second case, large tumor size, increased growth rate, looseness of the background myxoid matrix, and thinness of the tumor blood vessels with calcospherite deposition predisposed to vascular leakage and bleeding concurrent with sudden increases in intravascular hydrostatic pressure. In that cerebellar PAs are common, this report underscores the importance of considering in the differential diagnosis the possibility of a spontaneous hemorrhage in a posterior fossa PA in a child presenting with a sudden neurological ictus and raised ICP.
机译:毛细胞星形细胞瘤(PAs)的急性出血表现已得到越来越多的认识。由于后颅窝补偿质量效应的能力有限,导致快速的神经系统恶化,这种表现形式在最频繁出现的小脑PA出血中出现临床情况。作为示例,我们描述了两例致命的出血性小脑PA:一例儿童的症状呈缓慢增长的WHO WHO I级PA,症状期为1年,在临床快速恶化之前,另一例为无症状儿童,患有PA变体,在推测的瓦尔萨尔瓦事件后呈现渐进性闭塞。这两种情况与文献中先前的报道相类似,既有小脑功能障碍的进行性表达的设置和颅内压升高(ICP)的短暂发作,也有先前健康的孩子突然出现的ICP升高的特征。文献将作进一步回顾,以了解引起出血的易感因素,引发因素和目前传播的因素,并特别提及血管内皮生长因子和其他血管生成剂在PAs的脉管形成和稳定性中的作用。在这种情况下,我们认为在我们的第一种情况下,出血的发病机制是闭塞性血管壁透明质酸化以及相关的血流动力学改变和微动脉瘤形成。在第二种情况下,大肿瘤,生长速率增加,背景粘液样基质松散,肿瘤血管变薄并伴有钙铁矿沉积,易导致血管渗漏和出血,并伴有血管内静水压的突然升高。由于小脑PA是常见的,因此本报告强调了在鉴别诊断中考虑到突然出现神经性黄疸和ICP升高的儿童后颅窝PA自发性出血的可能性的重要性。

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