# A Rare Case of Eight-and-a-Half Syndrome Due to a Pontine Ischemic Stroke

**Authors:** Pedro L Almeida, Tiago Félix, Rafaela Evangelista, Ana Gomes, Ilídia Carmezim

PMC · DOI: 10.7759/cureus.85834 · Cureus · 2025-06-12

## TL;DR

This paper describes a rare neurological case involving a stroke in the brainstem, emphasizing the importance of clinical examination when imaging is unclear.

## Contribution

The paper presents a rare case of eight-and-a-half syndrome and highlights the role of clinical assessment in diagnosing uncommon brainstem strokes.

## Key findings

- A 77-year-old man presented with symptoms consistent with eight-and-a-half syndrome following a pontine ischemic stroke.
- Early neurological improvement was observed despite initially unremarkable CT imaging.
- The case underscores the value of clinical vigilance in diagnosing posterior circulation strokes.

## Abstract

Eight-and-a-half syndrome is an uncommon entity characterized by a combination of one-and-a-half syndrome and ipsilateral lower motor neuron facial palsy, typically resulting from a lesion in the dorsal pontine tegmentum. Although the clinical presentation may be striking, early diagnosis can be challenging due to subtle imaging findings in the hyperacute phase.

We report the case of a 77-year-old man with no prior disability who presented to the emergency department (ED) with the sudden onset of headache, dizziness, vomiting, diplopia, dysarthria, and gait instability. Neurological examination revealed left lower motor neuron facial palsy, impaired ocular motility with limited adduction of the left eye, horizontal nystagmus, upbeat and downbeat nystagmus, and severe gait ataxia. The clinical constellation was consistent with eight-and-a-half syndrome. A non-contrast CT scan was unremarkable; however, given the acute presentation, intravenous thrombolysis was administered. An MRI performed later confirmed an ischemic lesion in the dorsal pons. The patient showed early neurological improvement and was discharged with a minimal increase in disability. At the three-month follow-up, he remained independent with partial resolution of cranial nerve deficits.

We present this case to highlight the diagnostic value of detailed clinical examination in identifying uncommon brainstem syndromes, even when initial imaging is inconclusive. Recognition of eight-and-a-half syndrome at presentation can guide timely intervention and support clinical decision-making in the management of posterior circulation strokes. Documenting such cases enhances understanding of neuroanatomical correlations and reinforces the importance of clinical vigilance in acute stroke assessment.

## Linked entities

- **Diseases:** ischemic stroke (MONDO:1060198)

## Full-text entities

- **Diseases:** vomiting (MESH:D014839), acute stroke (MESH:D020521), gait instability (MESH:D043171), facial palsy (MESH:D005158), dysarthria (MESH:D004401), Pontine Ischemic Stroke (MESH:D020295), diplopia (MESH:D004172), ischemic lesion (MESH:D017202), headache (MESH:D006261), cranial nerve deficits (MESH:D003389), dizziness (MESH:D004244), horizontal nystagmus (MESH:D009759), impaired ocular motility (MESH:D015835), gait ataxia (MESH:D020234)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12254935/full.md

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Source: https://tomesphere.com/paper/PMC12254935