Parinaud syndrome

Last revised by Rohit Sharma on 6 Mar 2024

Parinaud syndrome, also known as dorsal midbrain syndrome, is a supranuclear vertical gaze disturbance caused by pathology of the dorsal midbrain region, often, but not exclusively, via compression of the superior tectal plate.

Parinaud syndrome is characterised by a classic triad of findings 4:

  • upward gaze palsy, often manifesting as diplopia

  • pupillary light-near dissociation (pupils respond to near stimuli, but not light)

  • convergence-retraction nystagmus

Other clinical features which may be present 4:

  • bilateral upper eyelid retraction (Collier sign)

  • downbeat nystagmus

Its importance lies in that recognition of Parinaud syndrome localises pathology to impingement of or origin in the tectal plate, most frequently due to a posterior commissure or pineal region mass (typically solid tumours rather than pineal cysts). However, Parinaud syndrome can also frequently be caused by haemorrhagic stroke, ischaemic stroke, demyelination, and other aetiologies 4.

Named after Henry Parinaud (1844-1905), a French ophthalmologist.

Cases and figures

  • Case 1: from pineal germinoma
  • Case 2: from pineal germinoma
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