首页> 外文期刊>Pediatric neurosurgery >Unusual case of 'trapped fourth ventricle' in a child with posthemorrhagic hydrocephalus - lessons learnt.
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Unusual case of 'trapped fourth ventricle' in a child with posthemorrhagic hydrocephalus - lessons learnt.

机译:失血后脑积水患儿异常的“被困第四脑室”病例-经验教训。

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In most of the children with posthemorrhagic hydrocephalus (PHH), multidisciplinary follow-up is performed, with the focus on consequences of prematurity, cerebral palsy (CP) and hydrocephalus. A large fourth ventricle is common in these children but imaging performed in order to document ventricles and tissue damage is not oriented to exclude coexisting rare pathologies. We report a 3-year-old child with spastic CP, secondary to prematurity and PHH. A ventriculoperitoneal shunt was inserted at the age of 2 months. On follow-up imaging the child demonstrated well-drained supratentorial ventricles with a persistent large fourth ventricle. Because of a neurological change in spasticity and new-onset torticollis, a repeat MRI was performed, suggesting a cystic, nonenhancing lesion of the fourth ventricle. The surgical exploration revealed a large dermoid of the fourth ventricle. We analyze the differential diagnosis of a clinically significant large fourth ventricle in a shunted child with PHH and CP. This includes conditions without pressure in the posterior fossa such as tissue loss due to cerebellar atrophy, or pathologies causing a true increase in pressure of the fourth ventricle (isolated fourth ventricle, cystic lesions and neoplasms of the fourth ventricle). Neurologically compromised children pose additional challenges in reaching a definitive diagnosis and hence require a careful regular assessment of their clinical status with additional well-timed imaging with appropriate protocols to allow appropriate treatment when indicated and to avoid morbidity due to delayed diagnosis. We present a rare coexistence of a dermoid tumor within the fourth ventricle in a CP child with PHH and express the dilemmas associated with its management.
机译:在大多数患有出血后脑积水(PHH)的儿童中,进行多学科随访,重点是早产,脑瘫(CP)和脑积水的后果。在这些儿童中,较大的第四脑室是常见的,但是为了记录脑室而进行的成像和组织损伤并不能排除并存的罕见病理。我们报告了一个3岁的儿童,患有痉挛性CP,继发于早产和PHH。 2个月大时插入心室腹膜分流术。在后续影像学检查中,儿童表现出排水良好的上脑室,并持续存在着较大的第四脑室。由于痉挛和新发作的斜颈的神经系统变化,因此进行了MRI重复检查,提示第四脑室为囊性,非增强性病变。手术探查发现第四脑室皮肤较大。我们分析了PHH和CP的分流儿童的临床上重要的第四脑室的鉴别诊断。这包括后颅窝无压力的情况,例如由于小脑萎缩引起的组织丢失,或导致第四脑室(孤立的第四脑室,囊性病变和第四脑室肿瘤)真正升高的病理。神经系统受损的儿童在做出明确的诊断时面临其他挑战,因此需要对他们的临床状况进行仔细的定期评估,并通过适当的方案进行额外的定时成像,以便在有指征时进行适当的治疗,并避免因诊断延迟而发病。我们提出了在患有PHH的CP儿童中,第四脑室中皮样肿瘤的罕见共存,并表达了与其管理相关的难题。

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