Find information on thousands of medical conditions and prescription drugs.

Horner's syndrome

Horner's syndrome is a clinical syndrome caused by damage to the sympathetic nervous system. more...

Home
Diseases
A
B
C
D
E
F
G
H
Hairy cell leukemia
Hallermann Streiff syndrome
Hallux valgus
Hantavirosis
Hantavirus pulmonary...
HARD syndrome
Harlequin type ichthyosis
Harpaxophobia
Hartnup disease
Hashimoto's thyroiditis
Hearing impairment
Hearing loss
Heart block
Heavy metal poisoning
Heliophobia
HELLP syndrome
Helminthiasis
Hemangioendothelioma
Hemangioma
Hemangiopericytoma
Hemifacial microsomia
Hemiplegia
Hemoglobinopathy
Hemoglobinuria
Hemolytic-uremic syndrome
Hemophilia A
Hemophobia
Hemorrhagic fever
Hemothorax
Hepatic encephalopathy
Hepatitis
Hepatitis A
Hepatitis B
Hepatitis C
Hepatitis D
Hepatoblastoma
Hepatocellular carcinoma
Hepatorenal syndrome
Hereditary amyloidosis
Hereditary angioedema
Hereditary ataxia
Hereditary ceroid...
Hereditary coproporphyria
Hereditary elliptocytosis
Hereditary fructose...
Hereditary hemochromatosis
Hereditary hemorrhagic...
Hereditary...
Hereditary spastic...
Hereditary spherocytosis
Hermansky-Pudlak syndrome
Hermaphroditism
Herpangina
Herpes zoster
Herpes zoster oticus
Herpetophobia
Heterophobia
Hiccups
Hidradenitis suppurativa
HIDS
Hip dysplasia
Hirschsprung's disease
Histoplasmosis
Hodgkin lymphoma
Hodgkin's disease
Hodophobia
Holocarboxylase...
Holoprosencephaly
Homocystinuria
Horner's syndrome
Horseshoe kidney
Howell-Evans syndrome
Human parvovirus B19...
Hunter syndrome
Huntington's disease
Hurler syndrome
Hutchinson Gilford...
Hutchinson-Gilford syndrome
Hydatidiform mole
Hydatidosis
Hydranencephaly
Hydrocephalus
Hydronephrosis
Hydrophobia
Hydrops fetalis
Hymenolepiasis
Hyperaldosteronism
Hyperammonemia
Hyperandrogenism
Hyperbilirubinemia
Hypercalcemia
Hypercholesterolemia
Hyperchylomicronemia
Hypereosinophilic syndrome
Hyperhidrosis
Hyperimmunoglobinemia D...
Hyperkalemia
Hyperkalemic periodic...
Hyperlipoproteinemia
Hyperlipoproteinemia type I
Hyperlipoproteinemia type II
Hyperlipoproteinemia type...
Hyperlipoproteinemia type IV
Hyperlipoproteinemia type V
Hyperlysinemia
Hyperparathyroidism
Hyperprolactinemia
Hyperreflexia
Hypertension
Hypertensive retinopathy
Hyperthermia
Hyperthyroidism
Hypertrophic cardiomyopathy
Hypoaldosteronism
Hypocalcemia
Hypochondrogenesis
Hypochondroplasia
Hypoglycemia
Hypogonadism
Hypokalemia
Hypokalemic periodic...
Hypoparathyroidism
Hypophosphatasia
Hypopituitarism
Hypoplastic left heart...
Hypoprothrombinemia
Hypothalamic dysfunction
Hypothermia
Hypothyroidism
Hypoxia
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
Medicines

Symptoms

It results in ptosis (drooping upper eyelid), miosis (constricted pupil), and occasionally enophthalmos (the impression that the eye is sunk in) and anhidrosis (decreased sweating) on one side of the face.

In children Horner's syndrome sometimes leads to a difference in eye color between the two eyes (heterochromia). This happens because a lack of sympathetic stimulation in childhood interferes with melanin pigmentation of the melanocytes in the superficial stroma of the iris.

History

It is named after Dr Johann Friedrich Horner (1831-1886), the Swiss ophthalmologist who first described the syndrome in 1869. Several others had previously described cases, but "Horner's syndrome" is most prevalent. In France, Claude Bernard is also eponymised with the condition being called "syndrome Bernard-Horner".

Causes

Horner's syndrome is usually acquired but may also be congenital. Although most causes are relatively benign, Horner's syndrome may reflect serious pathology in the neck or chest (such as a Pancoast tumor) and hence requires workup.

Horner's Syndrome is due to a deficiency of sympathetic activity. The site of lesion to the sympathetic outflow is on the ipsilateral side that the symptoms are on. The following are examples of conditions that cause the clinical appearance of Horner's Syndrome:

  • First-order neuron disorder: Central lesions that involve the hypothalamospinal 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 the cavernous sinus).

Diagnosis

Three tests are useful in confirming the presence and severity of Horner's syndrome:

  1. Cocaine test - Cocaine blocks the reuptake of norepinephrine resulting in the dilation of a normal pupil. The pupil will fail to dilate in Horner's syndrome.
  2. Paredrine test
  3. Dilation lag test

Read more at Wikipedia.org


[List your site here Free!]


Thymic cyst presenting as Horner's syndrome
From CHEST, 4/1/92 by Guadalupe Fraile

Horner's syndrome consists of the classic clinical manifestations of miosis, partial ptosis, and apparent enophthalmos and is occasionally accompanied by anhidrosis and pain. The pupil is variably miotic, depending on the location, completeness, and chronicity of the deficit. Horner's syndrome may occur with a lesion anywhere along the oculosympathetic pathway.[1]

Thymic cysts are uncommon lesions derived from the thymopharyngeal duct. They usually are found in asymptomatic adults, although cardiac compression due to extrinsic pressure or rupture in the pericardial space and chest pain secondary to intracystic infection have been reported.[2-4]

We report a patient suffering from Horner's syndrome due to a cystic tumor of the thymus growing from the upper portion of the mediastinum into the neck. Horner's syndrome was due to extrinsic compression of the sympathetic plexus that accompanies the carotid. To our knowledge, there are no previous descriptions of thymic cysts leading to Horner's syndrome.

Case Report

A 64-year-old man was discovered by chance to have Horner's syndrome in January 1990. The patient did not remember when the onset of ptosis occurred. He was asymptomatic and had no previous history of migraine. On physical examination, the only positive findings were ptosis on the right and the fact that the right pupil was 2 mm smaller than the left. there was no evidence of anhidrosis or enophthalmos. Elemental blood analysis, an electrocardiographic study, and thyroid function test results were normal. Chest radiographs revealed superior mediastinal enlargement. Computed tomography of the thoracic inlet and neck revealed a large (12 cm in diameter), low-density mass, which deviated the right carotid artery to the right and the trachea to the left (Fig 1).

At surgery, the tumor was found to contain clear fluid and was completely excised via a cervical incision. Microscopic study disclosed a fibrotic membranous wall with thymic tissue (Fig 2) with no evidence of malignancy.

The patient recovered from surgery and six months later remained asymptomatic. On physical examination, ptosis had disappeared, and anisocoria was less evident than it had been initially.

Discussion

Horner's syndrome may occur with a lesion anywhere along the sympathetic pathway, but it usually results from cervical sympathetic chain compression by a malignant tumor. With a lesion of the brain stem or cervical spinal cord, other signs of neurologic dysfunction usually predominate. Second-order preganglionic involvement may occur with lesions of the superior mediastinum, the apex of the lung, or the neck, whereas postganglionic involvement may be the result of an abnormality of the internal carotid artery, a lesion in the middle cranial fossa or cavernous sinus, or a migraine equivalent.[1,5]

Thymic cysts may occur at any anatomic level, from near the base of the neck to the diaphragm. Although distant or discontinuous accessory lobes commonly occur within the anterior mediastinal and cervical regions, thymic cysts are often found near the base of the heart.[6,7] Thymomas often undergo cystic degeneration, at times so extensive as to result in a gross picture similar to that of a thymic cyst. Radiography does not allow distinction between benign thymic cysts and other potentially malignant lesions.[8] However, careful histologic examination of the cyst will invariably disclose residual tissue in its wall.[2] Thymic cysts should, therefore, be excised, principally to differentiate them from thymomas.

We believe that the most important clue to diagnosis of thymic cysts as the cause of Horner's syndrome is the clinical history. Thus, diagnosis may be suspected in asymptomatic subjects with mediastinal enlargement in whom Horner's syndrome is not accompanied by other neurologic signs or symptoms.

References

[1] Slamovits TL, Glaser JL. the pupils and accommodation. In: Duane TD, Jaeger EA, eds. Clinical ophthalmology (vol 2). Philadelphia: Lippincott, 1988; 1-26 [2] Jones KW, Pietra GG, Sabiston DC. Primary neoplasms and cysts of the mediastinum. In: Fishman AP, ed. Pulmonary diseases and disorders. New York: McGraw-Hill, 1980, 1490-521 [3] Smith SB. Thymus In: Anderson WAD, Kissane JM, eds. Pathology (vol 2), 7th ed. St Louis: CV Mosby, 1977; 1575-600 [4] San Millan J, Roldan Sanchez JR, Nunez V, Bogaert M, Larru E. Clinical and radiological aspects of mediastinal thymic cysts. Arch Bronchopneumol 1989; 25:314-17 [5] Beck RW. Disorders of the eye, visual system and oculomotor system. In: Kelley, ed. Textbook of internal medicine. Philadelphia: Lippincott, 1989; 464:2366-369 [6] Day DL, Gedgandas E. the thymus. Radiol Clin North Am 1984; 22:519-38 [7] Baron RL, Lee JK, Sagel SS, Levitt RG. Computed tomography of the abnormal thymus. Radiology 1982; 142:127-34 [8] Dunne MG, Weksberg AP. Thymic cyst: computed tomography and ultrasound correlation. CT 1983; 7:351-55

COPYRIGHT 1992 American College of Chest Physicians
COPYRIGHT 2004 Gale Group

Return to Horner's syndrome
Home Contact Resources Exchange Links ebay