Posterior reversible encephalopathy syndrome: a rare neurological manifestation in Von Hippel-Lindau disease.

Abstract:

:We report on a 34-year-old woman, who was recently diagnosed with Von Hippel-Lindau disease (VHL), genetically confirmed. At this moment, she presented with an acute history of arterial hypertension, headache, cortical blindness and epilepsy. On the basis of clinical and magnetic resonance imaging (MRI) criteria the diagnosis of a posterior reversible encephalopathy syndrome (PRES) was made. A iodine 123-Labeled metaiodobenzylguanidine (MIBG) scan revealed the presence of bilateral adrenal pheochromocytomas.

journal_name

Acta Clin Belg

journal_title

Acta clinica Belgica

authors

Vanacker P,Vanacker A,Leys A,Thijs V

doi

10.1179/acb.2010.060

subject

Has Abstract

pub_date

2010-07-01 00:00:00

pages

279-80

issue

4

eissn

1784-3286

issn

2295-3337

journal_volume

65

pub_type

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