Complete bilateral ophthalmoplegia in malignant intracranial hypertension in a child

被引:3
|
作者
Interlandi, Emanuela [1 ]
Pellegrini, Francesco [2 ]
De Luca, Marco [1 ]
Cerullo, Giovanni [3 ]
De Falco, Arturo [3 ]
De Marco, Rocco [1 ]
Tortori, Achille
Lee, Andrew G. [4 ,5 ,6 ,7 ,8 ,9 ,10 ,11 ]
机构
[1] Osped del Mare ASL Napoli 1 Ctr, Dept Ophthalmol, Naples, Campania, Italy
[2] Osped Santo Spirito, Dept Ophthalmol, Via Fonte Romana 8, I-65124 Pescara, PE, Italy
[3] Osped del Mare ASL Napoli 1Ctr, Dept Neurol, Naples, Campania, Italy
[4] Houston Methodist Hosp, Blanton Eye Inst, Dept Ophthalmol, Houston, TX 77030 USA
[5] Weill Cornell Med, Dept Ophthalmol Neurol & Neurosurg, New York, NY USA
[6] Univ Texas Med Branch, Dept Ophthalmol, Galveston, TX 77555 USA
[7] Univ Texas MD Anderson Canc Ctr, 1515 Holcombe Blvd, Houston, TX 77030 USA
[8] Texas A&M Coll Med, College Stn, TX USA
[9] Baylor Coll Med, Ctr Space Med, Houston, TX 77030 USA
[10] Univ Iowa Hosp & Clin, Iowa City, IA USA
[11] Univ Buffalo, Buffalo, NY USA
关键词
Neuro imaging; neuro-ophthalmology; optic neuropathy; neuro-ophthalmic disease; pediatric ophthalmology; eye movement disorders; strabismus; ocular motility disorders; NERVE PALSY;
D O I
10.1177/1120672120966562
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To describe a case of fulminant idiopathic intracranial hypertension (IIH) in a child with "malignant" presentation. Case report: A 16-year-old, previously healthy, girl presented with bilateral visual loss and bilateral global limitation of eye movements in the absence of headache. Extensive laboratory evaluation for infectious, inflammatory, autoimmune, and neoplastic conditions was negative. Magnetic resonance imaging (MRI) of the brain and lumbar puncture findings were consistent with a diagnosis of IIH. Extraocular motility improved in the next few days as well as optic disc edema but visual acuity remained poor. Conclusion: The authors believe that the acute, severe, and fulminant ("malignant") presentation with markedly elevated intracranial pressure may produce the unique presentation of severe vision loss and bilateral complete ophthalmoplegia. Interestingly, there was no headache. To our knowledge this is the first such case to be reported in the English language ophthalmic literature.
引用
收藏
页码:NP24 / NP27
页数:4
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