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ISCHEMIC STROKE AND ACUTE PEMPHIGUS - TWO PARTNERS IN CRIME.

Authors :
Gealapu, Maria Liliana
Enascuta, Ana Maria
Croitoru, Cristina Georgiana
Popa, Alexandra Liliana
Burtea, Cristina
Naconecinii, Daniel
Cuciureanu, Dan Iulian
Source :
Romanian Journal of Neurology. 2019, Vol. 18 Issue 3, p140-144. 5p.
Publication Year :
2019

Abstract

Introduction. Bullous dermatoses are a group of skin-specific autoimmune diseases with systemic involvment that have a molecular basis related to the development of IgG autoantibodies targeted against desmosome proteins. The purpose of this report consists in marking the association between an acute cerebrovascular event and an active phase blistering dermatosis, at a pacient with no other known risk factors. Case presentation. Female patient, 46 years old, diagnosed with pemphigus vulgaris one year before, was admitted to the emergency room with left hemiparesis. The general physical examination shows multiple fragile blisters with serocitrin content and well-defined painful skin erosion, localized on the limbs, thorax and abdomen. The neurological examination revealed a conscious, cooperative, right-handed pacient with left proportional flaccid hemiparesis, and homonimous hemianopya. Native cranio-cerebral computed-tomography described acute infarction in the right sylvian arterial territory. Extensive paraclinical tests did not reveal an evident pathogenesis of acute ischemic stroke. Conclusions. Patients with bullous dermatosis have a two-folded increased risk of stroke, particularly ischemic stroke and this risk remains high even after controlling modifiable cardiovascular risk factors. The neurologist should consider implementing primary ischemic stroke prevention in patients diagnosed with bullous dermatosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18438148
Volume :
18
Issue :
3
Database :
Academic Search Index
Journal :
Romanian Journal of Neurology
Publication Type :
Academic Journal
Accession number :
139787115
Full Text :
https://doi.org/10.37897/rjn.2019.3.7