SciELO - Scientific Electronic Library Online

 
vol.7 issue3Noninvasive Follicular Thyroid Neoplasm with Papillary-Like Features author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Gazeta Médica

Print version ISSN 2183-8135On-line version ISSN 2184-0628

Abstract

MACHADO, Catarina et al. Behçet’s Disease Presenting with Cerebellar Involvement. Gaz Med [online]. 2020, vol.7, n.3, pp.272-276.  Epub July 01, 2021. ISSN 2183-8135.  https://doi.org/10.29315/gm.v7i3.269.

Behçet’s disease is a rare multisystemic vasculitis that most commonly presents with recurrent episodes of oral ulceration. However, other system involvement may be the first sign. We report a case of a 45-year-old male who presented with walking instability, loss of motor/sensory function on the upper left arm, vertigo and poor visual acuity. The magnetic resonance imaging showed an expansive lesion in the posterior fossa adjacent to the middle cerebellar peduncle. On ophthalmic examination, he presented occlusion of the inferior temporal vein. After a complete anamnesis, it was possible to establish a history of recurrent aphthous ulceration in the oral mucosa. Due to high suspicion of Behçet’s disease with neurological involvement, the patient was started on corticosteroids, with clinical, analytical and imagiologic improvement. Behçet’s disease can be very difficult to diagnose when the initial manifestation does not include the classic clinical triade of oral aphthous ulceration, genital ulcers and ocular disease.

Keywords : Behcet Syndrome; Nervous System Diseases.

        · abstract in Portuguese     · text in Portuguese     · Portuguese ( pdf )