Jump to content

Medial pontine syndrome

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by 2405:205:b001:5c22:81c5:afcc:2e95:87db (talk) at 17:17, 11 November 2024 (Diagnosis). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Medial pontine syndrome
Pons. (Medial pontine syndrome affects structures at the bottom of the diagram: the corticospinal tract, abducens nerve, and occasionally the facial nerve. Medial lemniscus is also affected, but not pictured.)
SpecialtyNeurology Edit this on Wikidata

Medial inferior pontine syndrome is a condition associated with a contralateral hemiplegia.[citation needed]"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.[citation needed]

Structure affected Presentation
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

Human brainstem blood supply description. Basilar artery is #7, and pons is visible below it.

Medial pontine syndrome results from occlusion of paramedian branches of the basilar artery.[citation needed]



Diagnosis

httfytygyg6

Treatment

See also

References

  1. ^ 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.