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伴有脊柱和神经根性疼痛的家族性特发性颅内高压

Familial idiopathic intracranial hypertension with spinal and radicular pain.

作者信息

Santinelli R, Tolone C, Toraldo R, Canino G, De Simone A, D'Avanzo M

机构信息

Department of Pediatrics, Second Pediatric Clinic, Second University of Naples, Italy.

出版信息

Arch Neurol. 1998 Jun;55(6):854-6. doi: 10.1001/archneur.55.6.854.

DOI:10.1001/archneur.55.6.854
PMID:9626778
Abstract

OBJECTIVE

To describe a mother and her 2 sons affected by idiopathic intracranial hypertension (IIH), associated in the sons with root irritation symptom. Unlike the other 4 families reported previously, obesity was not present in our patients.

DESIGN

Case reports.

SETTING

Department of pediatrics in a university school of Medicine, Naples, Italy.

PATIENTS

A mother (aged 36 years) and her 2 sons (aged 14 and 9 years) developed IIH at different times. Neuroimaging showed an empty sella in the mother, while IIH was associated with spinal and radicular pain in her 2 sons. The mother and the younger son developed permanent visual loss.

CONCLUSIONS

Ophthalmologic follow-up in our patients indicates that IIH is a chronic disease. Surgical treatment should be considered an option.

摘要

目的

描述一位母亲及其两名受特发性颅内高压(IIH)影响的儿子,儿子伴有神经根刺激症状。与之前报道的其他4个家庭不同,我们的患者并不肥胖。

设计

病例报告。

地点

意大利那不勒斯一所大学医学院的儿科。

患者

一位母亲(36岁)及其两名儿子(14岁和9岁)在不同时间患上IIH。神经影像学显示母亲有垂体空泡蝶鞍,而她的两名儿子的IIH伴有脊柱和神经根疼痛。母亲和小儿子出现了永久性视力丧失。

结论

我们患者的眼科随访表明IIH是一种慢性疾病。应考虑将手术治疗作为一种选择。

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