Ramsay Hunt syndrome type 2

Early symptoms include intense pain in one ear, the jaw on one side or the neck on one side which may precede the acute facial paralysis by a week or more.

Acute symptoms include:

• acute facial nerve paralysis
• pain in the ear, jaw and/or neck
• taste loss in the front two-thirds of the tongue
• dry mouth and eyes
• an erythematous vesicular rash in the ear canal, the tongue, and/or hard palate.[2]

Because the vestibulocochlear nerve is in proximity to the geniculate ganglion, it may also be affected and patients may also experience:

• tinnitus
• hearing loss
• hyperacusis
• vertigo

The swallow reflex might also be affected.

Involvement of the trigeminal nerve can cause numbness of the face.

The varicella zoster virus infects people and results in a distributed vesicular rash with fever, known as chickenpox. Respiratory droplets are the main method of virus transmission during the acute stage of the infection. After it subsides, it stays dormant in nerve cells in the body. It may reactivate under conditions of physiological stress or if the immune system is suppressed in any way (for example during an illness or undergoing chemotherapy), resulting in herpes zoster, also known as shingles or Ramsay Hunt syndrome when facial paralysis in involved. If the nerve cells affected lie within the facial nerves, it causes the symptoms described above.[3][4]

Ramsay Hunt Syndrome Type 2 is estimated to account for 12% of all facial nerve paralysis.[5] It occurs in both immunocompetent and immunocompromised individuals with immunocompromised patients often having more severe disease presentation. RHS may occur in any age group with cases reported in patients ranging in age from 3 months to 82 years.

The affected ganglion is responsible for the movements of facial muscles, the touch sensation of a part of ear and ear canal, the taste function of the frontal two-thirds of the tongue, and the moisturization of the eyes and the mouth. The syndrome specifically refers to the combination of this entity with weakness of the muscles activated by the facial nerve. In isolation, the latter is called Bell's palsy.[6]

However, as with shingles, the lack of lesions does not definitely exclude the existence of a herpes infection. Even before the eruption of vesicles, varicella zoster virus can be detected from the skin of the ear.

Ramsay Hunt Syndrome Type 2 can be diagnosed based on clinical features; however, in ambiguous cases, PCR or direct immunofluorescent assay of vesicular fluid can help with the diagnosis. Laboratory studies such as WBC count, ESR and electrolytes can distinguish infectious versus inflammatory etiologies.

Shingles is prevented by immunizing against the causal virus, varicella zoster, using a zoster vaccine. Vaccination is recommended for adults 50 and older.[8] Two versions of the vaccine are available, the live attenuated Zostavax (now discontinued in the US, essentially a larger-dose chickenpox vaccine) and the protein subunit Shingrix.[9]

Treatments for Ramsey Hunt Syndrome Type 2 are used to reduce further damage caused by the viral infection. These medications will not reverse any damage that has already occurred at the time that they are prescribed. Initial treatment with a corticosteroid such as prednisone and an antiviral drug such as acyclovir, valacyclovir or famciclovir for 5 to 7 days is standard; however, some studies have shown later damage to the facial nerve and recommend 21 days of antivirals.[5][2] Studies indicate that treatment started within 72 hours of the onset of facial paralysis improves the chances of the patient experiencing significant recovery.[10] Chances of recovery appear to decrease when treatment is delayed. Delay of treatment may result in permanent facial nerve paralysis. However, some studies demonstrate that even when steroids are started promptly, only 22% of all patients achieve full recovery of facial paralysis.[11] Treatment apparently has no effect on the recovery of hearing loss.

Meclizine, benzodiazepines such as diazepam, and vestibular therapy are sometimes used to treat the vertigo.

During the acute recovery phase, the eye on the affected side of the face may not blink completely or at all and may not close tightly or at all when sleeping. If the eye is dry or feels irritated, this is a strong indication that the eye is not properly blinking or closing completely. Using artificial tears every 5 to 20 minutes while awake and protecting the eye while asleep are very important to maintaining the health of the eye. While asleep, applying overnight eye gel and using sensitive skin medical tape or an eye patch to keep the eye closed or using a moisture chamber can protect the eye. Taking these precautions is extremely important to preserve the health and functionality of the eye and prevent corneal abrasions and corneal ulcers.[2]

Nerve pain associated with Ramsay Hunt Syndrome may be extreme and centered in the ear, neck, cheek, jaw and face. This nerve pain may not respond well to standard pain treatments including NSAIDS and opioids. Medication specifically for nerve pain such as tricyclic antidepressants and gabapentin have been shown to be effective for the neuropathic pain and post-herpetic neuralgia common with RHS.[2]

Physical therapy, excessive movement or electrical stimulation practiced during the first year of recovery greatly increase the chances of long term complications, including hyperactive muscles and synkinesis, both of which are permanent. The most common form of synkinesis for Ramsay Hunt Syndrome patients involves the eye being connected to the mouth (i.e. blinking while speaking, tearing while eating) and chin dimpling (chin dimples forming when speaking). Many forms of synkinesis can be managed with use of medical Botox administered by a qualified doctor.[12]

Overall between 30% and 70% of Ramsay Hunt syndrome type 2 patients recover most functionality depending on early diagnosis and treatment with chances of recovery dropping to 50% if treatment is delayed beyond 72 hours.[2]

Once the active infection has been cleared with antivirals, the facial nerves will begin to regrow at approximately 1mm per day. The recovery process for Ramsay Hunt syndrome is significantly longer than Bell's palsy. On average, Ramsay Hunt syndrome patients begin to see their symptoms resolve between 5 and 12 months post diagnosis and can expect to see continued resolution of symptoms for up to 2 years post diagnosis. Occasionally, patients may experience minor improvements beyond 2 years. The order in which symptoms resolve is highly individual. Although most patients will experience some recovery; complete recoveries with no lingering symptoms are in the minority. The main factors affecting the overall prognosis are the severity of symptoms at onset, the age and general health of the patient and the timing of initial treatments

Common long term effects include:

• Permanent facial paralysis of some or all of the affected facial nerves
• Corneal abrasion and/or ulcers if proper care is not taken of the affected eye which may affect long-term vision
• Neuropathic pain and post-herpetic neuralgia can commonly persist for more than 3 months and a year to 18 months is not uncommon. More than 50% of patients report experiencing post-herpetic neuralgia.[2]
• Post-herpetic fatigue is also a common long term side effect and may persist for several months to a year or more.
• Weakness in the affected facial muscles
• Sensitivity to cold and heat in the affected facial muscles
• Synkinesis including eye fluttering, chin dimpling and eye watering
• Hyperactive muscles that contract inappropriately

Less common long term effects include:

• Verbal processing deficits including speaking the incorrect word (aphasia)
• Memory deficits including failures in short-term memory
• Vertigo
• Partial or full hearing loss
• Hyperacusis
• Hyperactive muscles particularly in the neck and cheek
• Tinnitus

Some patients report an increased sensitivity to barometric pressure with changes in weather patterns causing pain on the affected side of the face.

The syndrome is named for James Ramsay Hunt, the neurologist who first described it.[13][14]

In 10 June 2022 Canadian singer Justin Bieber announced that that he had been diagnosed with the condition. In a video posted on Instagram he said that the virus had affected nerves in his ear and face, and that his right eye was not blinking.[15] He has since entered treatment.[16]

• NINDS Herpes Zoster Oticus Information Page National Institute of Neurological Disorders and Stroke
• Vaccine at Centers for Disease Control and Prevention