Foster Kennedy syndrome

Foster Kennedy syndrome
Other names	Gowers–Paton–Kennedy syndrome, Kennedy's phenomenon, Kennedy's syndrome
Frontal lobe (on the right)
Specialty	Neurology

Foster Kennedy syndrome is a constellation of findings associated with tumors of the frontal lobe.^[1]

Although Foster Kennedy syndrome is sometimes called "Kennedy syndrome",^[2] it should not be confused with Kennedy disease, or spinal and bulbar muscular atrophy, which is named after .

Pseudo-Foster Kennedy syndrome is defined as one-sided optic atrophy with papilledema in the other eye but with the absence of a mass.^[3]

Presentation[]

The syndrome is defined as the following changes:^{[citation needed]}

• optic atrophy in the ipsilateral eye
• disc edema in the contralateral eye
• central scotoma (loss of vision in the middle of the visual fields) in the ipsilateral eye
• anosmia (loss of smell) ipsilaterally

This syndrome is due to optic nerve compression, olfactory nerve compression, and increased intracranial pressure (ICP) secondary to a mass (such as meningioma or plasmacytoma, usually an olfactory groove meningioma).^[4][5] There are other symptoms present in some cases such as nausea and vomiting, memory loss and emotional lability (i.e., frontal lobe signs).^[5]

Diagnosis[]

Brain tumor can be visualized very well on CT scan, but MRI gives better detail and is the preferred study. Clinical localization of brain tumors may be possible by virtue of specific neurologic deficits or symptom patterns. Tumor at the base of the frontal lobe produces inappropriate behavior, optic nerve atrophy on the side of the tumor, papilledema on the other side, and anosmia.^{[citation needed]}

Treatment[]

The treatment, and therefore prognosis, varies depending upon the underlying tumour.^[5] While awaiting surgical removal, treat any increased intracranial pressure with high-dose steroids (i.e., dexamethasone).^{[citation needed]}

History[]

The syndrome was first extensively noted by Robert Foster Kennedy in 1911, an Irish neurologist, who spent most of his career working in the United States of America.^[6] However, the first mention of the syndrome came from a William Gowers in 1893. Schultz–Zehden described the symptoms again in 1905. A later description was written by Wilhelm Uhthoff in 1915.^[7]

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