Shingles – The Sleeping Monster, Part 1
Hearing Health & Technology Matters
June 27, 2017

Some readers may be surprised at today’s topic and wonder what shingles has to do with hearing loss or balance problems.    Shingles is a huge topic on its own, not to mention how it affects hearing and balance. Today’s post is a Q&A overview.  Future posts will be more specific about shingles, hearing, and balance problems.


What is/are shingles

It’s a viral infection called Herpes zoster.  It is not contagious.  It only occurs in people who have had chickenpox.  Even though it sounds plural, it is singular: saying “Shingles is horrible” is correct (and true).

Chickenpox rash is usually all over the body

What’s the difference between chickenpox and shingles?   Both disorders cause skin lesions/rashes.  Chickenpox and shingles used to be considered separate diseases but now we know they’re both caused by the varicella-zoster virus and both disorders can affect the same nerves.

OK, so what’s chickenpox?  It used to be called varicella and is considered the  “primary” infection of the virus.  Chickenpox is highly contagious, communicating by airborne transmission of the varicella-zoster virus, which enters people’s noses and travels into their bloodstreams before settling in on their nervous systems.

Chickenpox is a disease of childhood (75-90% of cases in children under 10) that manifests in rashes over much of the body.  The rashes are very itchy but rarely painful. That’s because children’s immune systems are “naive”–they lack a prepared immune response to launch an all-out war on the virus.    As a result,  nerve cell inflammation is minor with little or no cell death.  It’s a vanishing ailment, thanks to early immunization one or two doses of chickenpox vaccine.

This is getting confusing.  Tell me again, what’s shingles?   Shingles is confusing because of what happens when chickenpox is supposedly over. Nobody told us the cruel truth when we were kids, but the virus stays in the body for life and–like they say in the monster movies — IT’S ALIVE!  As long as the monster stays asleep in the deep (latent), it is nameless, but if awakened and provoked it is called shingles (herpes zoster). 

Where is it?  During latency, the inactive varicella virus literally hides in plain sight from the immune system, tucked away in cranial nerves and nerve bundles in the body called dorsal root ganglia which transmit sensory information from the skin to the brain.

How do you get shingles?  The only people who can get shingles are those who were previously infected with the chickenpox varicella virus.  If you haven’t had chickenpox, you can’t get Shingles, but you can get chickenpox.  If you have had chickenpox, you only get shingles if the virus wakes up.  You can’t get shingles from someone else who has it, but you can get chickenpox from a person with shingles if you haven’t had chickenpox.

How do I keep the virus asleep?  Nobody knows why the virus gets restless (“reactivates”) in some people and not in others.

What reactivates the virus?  It’s an equal opportunity monster as far as gender, race, and seasonality go.  But, reactivation is more common as we age; also in people with immune systems that are compromised by a variety of factors (e.g., HIV-positive, cancer, immunosuppressant drug treatments).   Table 1 gives a few statistics.

What happens when the virus reactivates and manifests as shingles?  The virus leaves home and spreads through the ganglion and nerves, especially those innervating the face and body trunk.  It can even invade the spinal cord and bloodstream.

What are the symptoms of shingles?  They are horrible. Although pain may precede it, shingles starts with a rash of small blisters that continue to develop for up to 5 days.  The blisters “follow” the nerve path on which the virus has settled, showing a band-like pattern in a particular skin area, distributed over the entire path of the nerve or restricted to separate areas.  Over a 3-4 week period, the blisters pop, ooze, crust and heal.  Throughout that time and in some cases for months afterward, there is:

  • Continuous burning or aching pain
  • Periodic piercing pain
  • Spasm similar to electric shock

Symptoms can be even more painful than “regular” pain, sometimes initiated by lightest of touch (e.g., clothing touching the body), temperature changes, or cold wind.  Symptoms can be especially bad at night.  Some people experience these symptoms for months after the outbreak.

What about prevention?  There is no cure, but a new vaccine is available (Zostavax), which the CDC recommends for routine one-time administration in people aged 60 and up.  Clinical trials suggest the vaccine reduces shingles outbreaks by about 50% and is effective for at least 6 years. The vaccine is approved by the FDA for those 50 and older. Unfortunately, people with suppressed immune systems are not candidates for the vaccine.

Can shingles affect hearing or balance?  It can.  When it settles on the vestibulocochlear nerve, the virus can chose one of several paths, with different consequences for the patient’s hearing and balance.  That is the topic of part 2 in the Shingles Series of posts.


References:  in addition to the links shown in the text information was pulled from a variety of sources including a Q&A and an In-depth Report in the NYTimes and Q&A at Yahoo and medicinenet. feature image from Mayo Clinic

  1. As a long time (March 2008) survivor of Ramsay Hunt Syndrome I am looking forward to reading your upcoming articles. I, like many RHS’ers, am left with disabling balance/dizziness issues. Originally misdiagnosed with cellulitus and Bell’s Palsy, I never did receive the Shingles strength of antivirals (I was seen at three different ER’s and then my local docs). I suspect that if I did my residuals would not be so severe. This is a common problem, even today. Most doctors don’t know what RHS is or how to treat it. To make matters worse, standard VT and hearing aids don’t seem to help us. When to start facial therapy, acupuncture, vitamin supplements, use of TENS, surgeries all seem to be trial and error. I was lucky, my hearing has returned to normal limits but I still have difficulty understanding some female voices (I had sensorineural loss). There are many who have become deaf on their RHS side with no relief. Seeing a Neurotologist seems to be our best shot at recovery, most other specialities just don’t understand our issues.
    I anxiously await your series and thank you for bringing this subject to light.

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