Article Text
Abstract
The anatomical localisation of brainstem syndromes is the domain of the clinical neurologist, though MRI has made an encyclopaedic knowledge of neuroanatomy less crucial. Isolated pontine syndromes comprise ∼20% of the brainstem lacunar syndromes. Typical presentations such as pure motor hemiparesis and ataxic hemiparesis are easily recognisable but atypical syndromes, particularly when bilateral, may present with puzzling signs. We discuss a patient with an unusual acute bilateral brainstem syndrome, in whom MRI was contraindicated. We use the relevant neuroanatomy to support the likely diagnosis of bilateral caudal pontine tegmentum infarction due to occlusion of a single paramedian pontine tegmental perforating artery.
- NEUROANATOMY
- STROKE
- EYE MOVEMENTS
- CLINICAL NEUROLOGY
Statistics from Altmetric.com
Footnotes
Contributors MRBE drafted the paper. MRBE and RAW edited the paper and are responsible for the final version. RAW is the neurologist caring for the patient.
Competing interests None declared.
Patient consent Obtained.
Provenance and peer review Commissioned; externally peer reviewed. This paper was reviewed by Tom Hughes, Cardiff, UK.
▸ References to this paper are available online at http://pn.bmj.com
Linked Articles
- Editors' commentary
Read the full text or download the PDF:
Other content recommended for you
- Double vision and facial palsy
- Internuclear ophthalmoplegia
- Bilateral paramedian pontine infarcts: a rare cause of bilateral horizontal gaze palsy
- Diplopia and eye movement disorders
- Blood, brain and binocular vision
- Eight-and-a-half syndrome: a rare presentation
- Rare occurrence of eight-and-a-half syndrome as a clinically isolated syndrome
- Wall eyed bilateral internuclear ophthalmoplegia (WEBINO) syndrome as a false localising sign in intracranial haemorrhage due to snake bite
- Complete bilateral horizontal gaze paralysis disclosing multiple sclerosis
- Eyes and stroke: the visual aspects of cerebrovascular disease