Horner Syndrome

Diagnosis isn’t the challenge—finding the cause is - Jessica Steen OD and Joseph Sowka OD

Horner Syndrome
Horner Syndrome

image by: Syrian Board of Ophthalmology

HWN Suggests

Horner’s Syndrome: A Positive Apraclonidine Test—Now What?

Historically, topical liquid 10% cocaine was used to identify the presence of Horner’s syndrome, and topical hydroxyamphetamine was used to aid in localizing a postganglionic lesion. Today, these agents are not practically available; instead, the diagnosis of a suspected Horner’s syndrome can be confirmed by pharmacological testing with apraclonidine 0.5% or 1%.

In Horner’s syndrome, the affected pupil and levator undergo denervation hypersensitivity. Apraclonidine is an alpha-2 adrenergic agonist that also acts as a very weak alpha 1-adrenergic agonist; when topically applied in Horner’s syndrome, it causes dilation of the affected pupil and possibly lid elevation, without change…

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 Horner’s Syndrome: A Positive Apraclonidine Test—Now What?

In Horner’s syndrome, the affected pupil and levator undergo denervation hypersensitivity. Apraclonidine is an alpha-2 adrenergic agonist that also acts as a very weak alpha 1-adrenergic agonist; when topically applied in Horner’s syndrome, it causes dilation of the affected pupil and possibly lid elevation, without change to the normal pupil. These changes are so dramatic that a ‘reversal’ occurs; the normal pupil and lid now appear ptotic and miotic in comparison with the apraclonidine-positive eye.

MedComic

Horner syndrome results from disruption of the sympathetic pathway that runs from the hypothalamus to the eye. Classic signs include miosis, ptosis, and anhidrosis of the affected side. Causes include brain tumor, brain stem infarct, pancoast tumor, cervical adenopathy, skull and neck trauma, carotid dissection, and thoracic aortic aneurysm. Instilling cocaine or apraclonidine drops into both eyes can confirm the diagnosis of Horner syndrome. Imaging studies such as MRI, CT, or MRA may be obtained based on the history and physical exam. Treatment depends on the underlying cause of Horner syndrome.

Case report and literature review: Horner syndrome subsequent to endoscopic thyroid surgery

Horner syndrome (HS), mainly characterized by symptoms including ptosis, miosis, and anhidrosis on the affected face, is a condition that is well documented but rarely reported as a postoperative complication of thyroidectomy, particularly in endoscopic thyroid surgery (ETS).

HealthEngine

Horner syndrome is an uncommon to rare condition. There is no statistical data on the incidence of Horner syndrome because it is the causative factor that is important.

Life in the Fastlane

Johann Friedrich Horner (1831-1886) reported the findings of ptosis, miosis, and enophthalmos in a 40-year-old peasant woman. He also observed increased skin temperature and dryness of the ipsilateral face. He pharmacologically confirmed the impairment of sympathetic innervation to the eye after noting poor dilation of the affected pupil following instillation of atropine and preserved pupillary constriction to the parasympathomimetic agent calabar.

Patient

Ipsilateral dry skin on the face due to loss of sweating: Take both index fingers and place then together in the middle of the forehead. Then run them laterally over the forehead to just lateral to the eyebrows. On the affected side there may be more friction as the skin is drier because there is no sweating on that side.

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