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Presentation, investigation and management of idiopathic intracranial hypertension in children

机译:儿童特发性颅内高压的表现,调查与处理

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Idiopathic intracranial hypertension is characterised by increased intracranial pressure in the presence of normal cerebrospinal fluid, normal neuroimaging and no localising signs on neurologic exam except cranial nerve VI palsy. It is common in adults, particularly obese young women, but also occurs in children and adolescents. We discuss the clinical presentation of idiopathic intracranial hypertension in the pediatric population and how the presenting signs and symptoms may be different from those seen in adult patients. We discuss the differential diagnosis for idiopathic intracranial hypertension, as well as underlying conditions that may be associated with it. As in adults, therapy most often involves the use of carbonic anhydrase inhibitors, diuretics, and steroids. Children with vision loss due to idiopathic intracranial hypertension who not respond to aggressive medical therapy should be promptly referred for surgical intervention, including optic nerve fenestration and cerebrospinal (CSF) shunting procedures such as ventriculoper-itoneal or lumboperitoneal shunting.
机译:特发性颅内高压的特征是在存在正常的脑脊髓液,正常的神经影像学检查和无神经系统检查的局部体征的情况下,颅内压增高,颅内VI麻痹。它常见于成人,特别是肥胖的年轻女性,但也发生于儿童和青少年。我们讨论了小儿人群中特发性颅内高压的临床表现,以及所表现出的体征和症状可能与成年患者中所见的有所不同。我们讨论了特发性颅内高压的鉴别诊断,以及可能与之相关的潜在疾病。与成人一样,治疗通常涉及使用碳酸酐酶抑制剂,利尿剂和类固醇。因特发性颅内高压而导致视力丧失的儿童,如果对积极的药物治疗没有反应,应立即转介其进行手术干预,包括视神经开窗和脑脊液(CSF)分流程序,如脑室腹膜或腰腹膜分流。

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