Foster-Kennedy Syndrome

Foster-Kennedy Syndrome

Foster-Kennedy syndrome is a condition in which one eye develops optic atrophy, whereas the other one develops papilledema; due to the presence of an intracranial mass. It is an extremely rare disorder.

Causes and risk factors

This condition is usually caused due to a frontal lobe tumor. Sometimes tumors from other sites may also be responsible.

Clinical presentation

One eye presents with optic atrophy, whereas the other eye presents with papilledema. The patient may develop central scotoma (loss of central vision), or sometimes even anosmia (loss of smell).

Additionally, the patient may develop other symptoms as a result of the intracranial tumor such as headache.

Investigations

Eye examination through fundoscopy is performed.

CT or MRI of the brain helps to detect the underlying tumor.

Treatment

The treatment is determined on the basis of the type and location of tumor. It may involve surgical excision of the tumor or radiation/chemotherapy.

When to contact a doctor

Contact a doctor as soon as you experience any visual problems, especially when associated with headache.

Facts and figures

1 to 2.5% of patients with intracranial masses may develop Foster-Kennedy syndrome.

Systems involved

Ophthalmic system, nervous system.

Organs involved

Eye, brain

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