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Medical Forum / Diseases and Disorders / Herpes / May 2006

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worried about herpes on hand

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badhand - 20 May 2006 13:23 GMT
For the last 4 years I have suffered bout fo blisters and then ulcers
on my arms and hands.
At first I suspected a contact dermatitis, then strimmer rash but both
these explanations were discarded through elimination.
I had read on the internet about polymorphic light eruption and I was
happy to agree with a dermatologist that this was the explanation. (By
the time I saw the dermatolgist of course i had nothing but photographs
to show)
I combat it by using lots of high factor sunblock and stay covered up.
A problem i have is that all images and descriptions of my blisters etc
dont really match up with  what i actually have.
Recently a friend and herpes sufferer commented that my blisters looked
suspiciously like herpes simplex.
My symptoms are exactly as a herpes sufferer. Tingling, small blisters,
larger blisters, ulcers and final;ly scabbing over.
I have these blisters where i fail to use sunblock and get exposed to
the sun. They can quite easily cover my entire arm and hand. At the
monent I have a patch of them covering the entire back of my left hand
and many along my fingers.

Any one else suffer like this? Is it likely to be herpes? This si
important to me as I do not wish to apss it on to anyone. PMLE is non
contagious.
grant - 20 May 2006 23:35 GMT
The only way to find out if it is herpes is to have the doctor culture one
of the lesions.  Period.  That's the only way.  It really doesn't matter
what it feels like or what it looks like because we are all so different.
Now, you can have a herpes blood test run and it will tell you if you have
herpes.  But that won't tell you if what you are experiencing on your arms
and hands is herpes.

Your outbreaks sound far more severe than the normal herpes outbreak.  But
your doctor should be running tests.

ar

> For the last 4 years I have suffered bout fo blisters and then ulcers
> on my arms and hands.
[quoted text clipped - 19 lines]
> important to me as I do not wish to apss it on to anyone. PMLE is non
> contagious.
 
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