Horner Syndrome - Clinical Features And Management

Horner syndrome (miosis, ptosis, and anhidrosis) is secondary to loss of ocular sympathetic innervation.

• Ptosis is less than 2 mm, the result of paralysis of Müller muscle, innervated by the sympathetic pathway. 
• Anhidrosis is often not apparent to patients or clinicians. 
• A pupillary finding specific in Horner syndrome is dilation lag. Because the dilator muscle is weak,
• the pupil dilates more slowly than the normal pupil.

This loss of ocular sympathetic innervation can be produced by a lesion anywhere along a three-neuron sympathetic pathway, from the hypothalamus down through the brain stem to the cervical cord, in the apex of the chest, along the carotid sheath, and in the cavernous sinus or orbit.
Isolated Horner syndrome presenting with head or neck pain suggests an internal carotid artery dissection.

Management
Associated signs and symptoms help direct the workup. A patient with cranial nerve abnormalities requires CT or MRI imaging and admission. In the setting of cervical spine trauma, neck immobilization and appropriate imaging studies are instituted. Consider carotid artery dissection in neck pain without trauma.


Points To Remember
1. Classic signs of a Horner syndrome include miosis and mild ptosis. Anhidrosis is less readily appreciated, and occurs with first- or second-order lesions only.
2. Miosis and dilation lag are accentuated in a darkened room.
3. A Pancoast tumor usually is caused by bronchogenic carcinoma and may present, as its presenting sign, as a Horner syndrome.
4. Cluster headaches, with autonomic sympathetic system dysfunction, are capable of producing an ipsilateral Horner syndrome.
5. Ipsilateral extraocular paresis, especially a sixth-nerve palsy, without other brainstem signs localizes pathology to within the cavernous sinus.