Foster-Kennedy syndrome digital illustration

Foster-Kennedy syndrome Save


ICD-10 code: H47.14

Chapter: Diseases of the eye and adnexia

Foster-Kennedy Syndrome: Symptoms, Causes, and Treatment

Foster-Kennedy syndrome is a rare medical condition that affects the optic nerve. It is named after two physicians, Sir William Richard Gowers Foster and Robert Kennedy, who first described the condition in 1911.

The syndrome is characterized by a combination of symptoms that include optic atrophy in one eye, papilledema in the other eye, and anosmia (loss of smell). The optic atrophy occurs in the eye with the tumor or lesion that compresses the optic nerve, while the papilledema occurs in the other eye due to increased intracranial pressure.

There are various causes of Foster-Kennedy syndrome, including tumors of the frontal lobe, meningiomas, and other lesions that compress the optic nerve. In rare cases, the syndrome can also be caused by non-neoplastic conditions such as inflammation, infection, or trauma.

  1. Symptoms: The most common symptoms of Foster-Kennedy syndrome include vision loss in one eye, papilledema in the other eye, and anosmia. Other symptoms may include headaches, nausea, vomiting, and seizures.
  2. Diagnosis: The diagnosis of Foster-Kennedy syndrome involves a comprehensive eye examination, neurological evaluation, and imaging studies such as CT scans or MRI.
  3. Treatment: The treatment of Foster-Kennedy syndrome depends on the underlying cause of the condition. In cases where the syndrome is caused by a tumor or lesion, surgical intervention may be necessary. In cases where the syndrome is caused by non-neoplastic conditions, medications such as corticosteroids may be prescribed to reduce inflammation and swelling.

It is essential to seek medical attention if you experience any of the symptoms associated with Foster-Kennedy syndrome. Early diagnosis and treatment can help prevent further damage to the optic nerve and improve the prognosis for the condition.

In conclusion, Foster-Kennedy syndrome is a rare medical condition that affects the optic nerve. It is characterized by a combination of symptoms that include optic atrophy in one eye, papilledema in the other eye, and anosmia. The syndrome can be caused by various factors, including tumors, lesions, inflammation, infection, or trauma. Early diagnosis and treatment are crucial for preventing further damage to the optic nerve and improving the prognosis for the condition.