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. 2017:35:17-22.
doi: 10.1007/8904_2016_18. Epub 2016 Nov 18.

Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children's Hospital

Affiliations

Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children's Hospital

Nieves Martín-Begué et al. JIMD Rep. 2017.

Abstract

Background: Cystinosis is a rare systemic lysosomal disease affecting mainly the kidney and eye. Ocular involvement in cystinosis is universal being the presence of cystine crystals in the cornea a diagnostic criterion and one of the earliest manifestations of the disease. Neuro-ophthalmologic manifestations are considered a rare and late complication in these patients. The aim of this article is to report the unexpectedly high incidence of intracranial hypertension in children with cystinosis at our centre.

Methods: This study included eight children (0-16 years of age) with cystinosis seen at the paediatric ophthalmology department, Hospital Universitari Vall d'Hebron (Barcelona, Spain), a tertiary hospital, over the last 5 years.

Results: Three girls and five boys, mean age: 9.6 years (range: 5-14 years), were studied. During follow-up, 4 out of 8 developed papilledema and confirmed high cerebrospinal fluid (CSF) pressure. The only symptomatic child presented an Arnold-Chiari anomaly with enlarged ventricles, whereas the other three, all asymptomatic, were diagnosed by scheduled fundoscopy and had normal neuroimaging studies. All four patients had at least one known risk factor for developing intracranial hypertension: initiation of growth hormone therapy, tapering of corticosteroids, acute renal failure and Arnold-Chiari malformation. Two of them required a ventriculoperitoneal shunt.

Conclusions: Our results show that intracranial hypertension can occur more frequently than expected in patients with cystinosis. Furthermore, visual prognosis depends on early diagnosis and prompt treatment. A multidisciplinary approach is necessary, and we recommend fundoscopic examinations in all paediatric patients with cystinosis whether or not they present symptoms.

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Conflict of interest statement

Nieves Martín-Begué, Silvia Alarcón, Charlotte Wolley-Dod, Luis Enrique Lara, Álvaro Madrid, Paola Cano, Mireia del Toro and Gema Ariceta declare that we have no conflict of interest.

Figures

Fig. 1
Fig. 1
Severe bilateral disc oedema with dilated veins, many exudates and multiple peripapillary and peripheral retinal haemorrhages in both eyes of Case 1 (right eye on the left and left eye on the right)
Fig. 2
Fig. 2
MRI T2-weighted axial image showing distension of the perioptic subarachnoid space (arrow) and flattening of the posterior aspect of the globe in Case 2

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