Idiopathic intracranial hypertension without papilledema in children: A case series

K. Matheos, S. Dai
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Abstract

Papilledema has long been considered a hallmark of idiopathic intracranial hypertension, a disease defined by elevated intracranial pressure with indiscernible etiology. Papilledema is often seen in the pediatric population, and as such can lead to delays in diagnosis, and often misdiagnosis. Here, we describe three children who were confirmed to have idiopathic intracranial hypertension with raised intracranial pressure by repeated lumbar puncture or intracranial pressure monitoring, normal neuroimaging and absence of papilledema. All three cases had atypical clinical presentations with visual disturbances or photophobia. The patients had a normal body mass index. This case series demonstrates that idiopathic intracranial hypertension can manifest in the absence of clinically obvious papilledema, and has, as such, the potential to cause permanent visual loss if the diagnosis is missed.
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儿童特发性颅内高压无乳头水肿:一个病例系列
长期以来,乳头水肿一直被认为是特发性颅内高压的标志,这是一种病因不明的颅内压升高的疾病。乳头水肿常见于儿科人群,因此可导致诊断延误,并经常误诊。在这里,我们描述了三名儿童,他们通过反复腰椎穿刺或颅内压监测证实患有特发性颅内高压,颅内压升高,神经影像学正常,没有乳头水肿。三例均有不典型的临床表现,包括视力障碍或畏光。这些患者的体重指数正常。本病例系列表明,特发性颅内高压可以在没有临床上明显的乳头水肿的情况下表现出来,因此,如果误诊,有可能导致永久性视力丧失。
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