Gradenigo's syndrome

From WikiMD's Wellness Encyclopedia

Gradenigo's syndrome is a rare medical condition characterized by a triad of symptoms: suppurative otitis media, severe pain in the distribution of the first and second divisions of the trigeminal nerve, and abducens nerve palsy. It is named after the Italian otologist, Giuseppe Gradenigo, who first described the syndrome in 1907.

Symptoms[edit | edit source]

The primary symptoms of Gradenigo's syndrome include:

  • Otitis media: This is an infection or inflammation of the middle ear. This condition can cause severe pain and may be associated with a fever.
  • Trigeminal neuralgia: This is characterized by severe facial pain in the distribution of the trigeminal nerve. The pain is often described as a sharp, shooting, or electric shock-like sensation.
  • Abducens nerve palsy: This condition causes weakness or paralysis of the muscles that move the eye. It can result in double vision and other visual disturbances.

Causes[edit | edit source]

Gradenigo's syndrome is typically caused by the spread of an infection from the middle ear to the nearby bones and nerves. This can occur as a complication of chronic otitis media, especially if the infection is not adequately treated.

Diagnosis[edit | edit source]

The diagnosis of Gradenigo's syndrome is based on the characteristic triad of symptoms. Additional tests, such as a CT scan or MRI, may be used to confirm the diagnosis and assess the extent of the infection.

Treatment[edit | edit source]

The treatment of Gradenigo's syndrome typically involves antibiotics to treat the underlying infection. In some cases, surgery may be necessary to drain the infection and prevent further spread.

Prognosis[edit | edit source]

With prompt and appropriate treatment, the prognosis for Gradenigo's syndrome is generally good. However, if left untreated, the condition can lead to serious complications, including meningitis, brain abscess, and sepsis.

See also[edit | edit source]

Gradenigo's syndrome Resources
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Contributors: Prab R. Tumpati, MD