Medial pontine syndrome: Difference between revisions
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[[Image:Human brainstem blood supply description.JPG|thumb|Human brainstem blood supply description. [[Basilar artery]] is #7, and [[pons]] is visible below it.]] |
[[Image:Human brainstem blood supply description.JPG|thumb|Human brainstem blood supply description. [[Basilar artery]] is #7, and [[pons]] is visible below it.]] |
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Medial pontine syndrome results from occlusion of paramedian branches of the [[basilar artery]]. |
Medial pontine syndrome results from occlusion of paramedian branches of the [[basilar artery]]. |
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==Diagnosis== |
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==See also== |
==See also== |
Revision as of 16:17, 6 September 2017
Medial pontine syndrome | |
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Specialty | Neurology |
Medial inferior pontine syndrome is a condition associated with a contralateral hemiplegia.
"Medial inferior pontine syndrome" has been described as equivalent to Foville's syndrome.[1]
Presentation
Although medial pontine syndrome has many similarities to medial medullary syndrome, because it is located higher up the brainstem in the pons, it affects a different set of cranial nuclei.
Structure affected | Presentation |
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Corticospinal tract | Contralateral spastic hemiparesis |
Medial lemniscus | Contralateral PCML (aka DCML) pathway loss (tactile, vibration, and stereognosis) |
Abducens nerve | Strabismus (ipsilateral lateral rectus muscle paralysis - the affected eye looks down and towards the nose). Abducens nerve lesion localizes the lesion to inferior pons. |
Depending upon the size of the infarct, it can also involve the facial nerve.
Cause
Medial pontine syndrome results from occlusion of paramedian branches of the basilar artery.
Diagnosis
This section is empty. You can help by adding to it. |
See also
- Alternating hemiplegia of childhood
- Lateral medullary syndrome
- Lateral pontine syndrome
- Medial medullary syndrome
- Weber's syndrome
References
- ^ Hubloue I, Laureys S, Michotte A (September 1996). "A rare case of diplopia: medial inferior pontine syndrome or Foville's syndrome". Eur J Emerg Med. 3 (3): 194–8. doi:10.1097/00063110-199609000-00011. PMID 9023501.
External links