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  • A rare case of oculomotor nerve palsy from presumed cavernous angioma

A rare case of oculomotor nerve palsy from presumed cavernous angioma
Reviewed by Claire Howard

1 February 2019 | Claire Howard | EYE - Neuro-ophthalmology | Cavernous angioma, infant, oculomotor nerve, oculomotor nerve palsy, schwannoma

Cavernous angiomas of the cranial nerves are extremely rare, and those of the oculomotor (third) nerve are rarer still. The authors present a single case study of presumed cavernous angioma involving the subarachnoid portion of the left third nerve, which is the first reported case found in the literature. The patient is a three-month-old male infant who presented as an acute left third nerve palsy. He presented with acute onset of left eyelid ptosis, decreased extraocular motility with an associated left exotropia and hypotropia, and anisocoria with the left pupil larger and less reactive than the right. Magnetic resonance (MR) imaging revealed enlargement of the initial subarachnoid portion of the left oculomotor nerve. The child was followed without intervention and the palsy completely resolved. The authors report that it is therefore reasonable to follow patients with these lesions without intervention, given the poor functional outcome results with attempted surgical excision and the potential for spontaneous improvement.

Acute transient oculomotor nerve palsy from presumed cavernous angioma in an infant.
Blizzard ST, Collins ME, Miller NR.
NEURO-OPHTHALMOLOGY
2018;42(4):229-32.
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CONTRIBUTOR
Claire Howard

Salford Royal NHS Foundation Trust, Salford, UK.

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