- Horner's syndrome
Infobox_Disease
Name = PAGENAME
Caption = Left-sided Horner's syndrome
DiseasesDB = 6014
ICD10 = ICD10|G|90|2|g|90
ICD9 = ICD9|337.9
ICDO =
OMIM = 143000
MedlinePlus = 000708
eMedicineSubj = med
eMedicineTopic = 1029
eMedicine_mult = eMedicine2|oph|336 | MeshID = D006732Horner's syndrome is a clinical
syndrome caused by damage to thesympathetic nervous system . It is also known by the names Bernard-Horner syndrome or oculosympathetic palsy.igns
Signs found in all patients on affected side of face include ptosis (drooping upper eyelid from loss of sympathetic innervation to the Müller or
superior tarsal muscle cite book |author=Adams, Raymond Delacy; Victor, Maurice; Ropper, Allan H. |title=Adam and Victor's principles of neurology |publisher=McGraw-Hill |location=New York |year=2001 |pages= |isbn=0-07-067497-3 |oclc= |doi=] ), upside-down ptosis (slight elevation of the lower lid), andmiosis (constricted pupil) and dilation lag.Enophthalmos (the impression that the eye is sunk in) andanhidrosis (decreasedsweating ) on the affected side of the face, loss ofciliospinal reflex and blood shot conjunctiva may occur depending on the site of lesion. Also flushing of the face is common on the affected side of the face due to dilation of blood vessels under the skin.In children Horner's syndrome sometimes leads to a difference in eye color between the two eyes (
heterochromia ). [cite journal | author=Gesundheit B, Greenberg M | title=Medical mystery: brown eye and blue eye--the answer | journal=N Engl J Med | year=2005 | pages=2409–10 | volume=353 | issue=22 | pmid=16319395 | doi=10.1056/NEJM200512013532219] This happens because a lack of sympathetic stimulation in childhood interferes withmelanin pigmentation of themelanocyte s in the superficial stroma of the iris.History
It is named after
Johann Friedrich Horner , the Swiss ophthalmologist who first described the syndrome in 1869. [Horner JF. "Über eine Form von Ptosis." Klin Monatsbl Augenheilk 1869;7:193-8.] [WhoNamedIt|synd|1056] Several others had previously described cases, but "Horner's syndrome" is most prevalent. InFrance andItaly ,Claude Bernard is also eponymised with the condition ("Claude Bernard-Horner syndrome").Causes
Horner's syndrome is acquired as a result of pathology but may also be
congenital (inborn) oriatrogenic (caused by medical treatment). Although most causes are relatively benign, Horner's syndrome may reflect serious pathology in the neck or chest (such as aPancoast tumor (tumor in the apex of the lung) or thyrocervical venous dilatation).
* Due to lesion or compression of one side of the cervical or thoracic sympathetic chain which generates symptoms on theipsilateral (same side as lesion) side of the body.
*Lateral medullary syndrome
*Cluster headache - combination termed Horton's headache [cite web | author=Graff JM, Lee AG | title=Horner's Syndrome (due to Cluster Headache): 46 y.o. man presenting with headache and ptosis. | url=http://webeye.ophth.uiowa.edu/eyeforum/cases/case22.htm | work=Ophthalmology Grand Rounds | date=February 21, 2005 | publisher=The University of Iowa | accessdate=2006-09-22]
* Trauma - base of neck, usually blunt trauma, sometimes surgery.
*Middle ear infection
*Tumors - oftenbronchogenic carcinoma of the superior fissure (Pancoast tumor ) on apex of lung
*Aortic aneurysm , thoracic
*Neurofibromatosis type 1
*Goitre
*Dissecting aortic aneurysm
*Thyroid carcinoma
*Multiple sclerosis
*Carotid artery dissection
*Klumpke paralysis
*Cavernous sinus thrombosis
*Sympathectomy
*Syringomyelia
*Nerve block s, such as cervical plexus block, stellate ganglion or interscalene blockPathophysiology
Horner's syndrome is due to a deficiency of
sympathetic activity.The site of lesion to the sympathetic outflow is on theipsilateral side of the symptoms.The following are examples of conditions that cause the clinical appearance of Horner's syndrome:
*"First-order neuron disorder:" Central lesions that involve thehypothalamospinal pathway (e.g. transection of the cervical spinal cord).
*"Second-order neuron disorder:"Preganglionic lesions (e.g. compression of the sympathetic chain by a lung tumor).
*"Third-order neuron disorder:"Postganglionic lesions at the level of the internal carotid artery (e.g. a tumor in thecavernous sinus ).Diagnosis
Three tests are useful in confirming the presence and severity of Horner's syndrome:
#Cocaine drop test -Cocaine blocks the reuptake ofnorepinephrine resulting in the dilation of a normal pupil. Due to the lack of norepinephrine in the synaptic cleft, the pupil will fail to dilate in Horner's syndrome.
#Paredrine test:- This test helps to localize the cause of the miosis. If the 3rd order neuron (the last of 3 neurons in the pathway which ultimately discharges norepinephrine into the synaptic cleft) is intact, then the amphetamine causes neurotransmitter vesicle release, thus releasing norepinephrine into the synaptic cleft and resulting in robust mydriasis of the affected pupil. If the lesion itself is of the aforementioned 3rd order neuron, then the amphetamine will have no effect and the pupil remains constricted. There is no pharmacological test to differentiate between a 1st and 2nd order neuron lesion.
#Dilation lag testIt is important to distinguish the ptosis caused by Horner's syndrome from the ptosis caused by a lesion to the
oculomotor nerve . In the former, the ptosis occurs with a constricted pupil (due to a loss of sympathetics to the eye), whereas in the latter, the ptosis occurs with a dilated pupil (due to a loss of innervation to thesphincter pupillae ). In an actual clinical setting, however, these two different ptoses are fairly easy to distinguish. In addition to the blown pupil in a CNIII (oculomotor nerve ) lesion, this ptosis is much more severe, occasionally occluding the whole eye. The ptosis of Horner's syndrome can be quite mild or barely noticeable.When
anisocoria occurs and the examiner is unsure whether the abnormal pupil is the constricted or dilated one, if a one-sided ptosis is present then the abnormally sized pupil can be presumed to be the one on the side of the ptosis.ee also
*
Anisocoria References
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