LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Lichen Planus

 - UBBFriend: Email this page to someone!    
Author Topic: Lichen Planus
LMC3495
Member
Member # 12879

Icon 1 posted      Profile for LMC3495     Send New Private Message       Edit/Delete Post   Reply With Quote 
Anyone know if lichen planus is associated with lyme? It's inflammation in the mouth. My mother was diagnosed yesterday (she has lyme). The doc told her it was an immune problem and could be brought on by stress.
Posts: 22 | From Texas | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
hurtingramma
LymeNet Contributor
Member # 7770

Icon 1 posted      Profile for hurtingramma     Send New Private Message       Edit/Delete Post   Reply With Quote 
An immune problem? First I've heard of that. I had lichen planus many, many years ago, all over my body. It is a skin disease. To eradicate it, I had to use a cortisone cream nightly and wrap myself up in Saran Wrap to hold in the moisture. Took many weeks to get rid of. And boy, did it itch.


Medical Dictionary
One entry found for lichen planus.


Main Entry: lichen pla�nus
Pronunciation: -pl-ns
Function: noun
: a skin disease characterized by an eruption of wide flat papules covered by a horny glazed film, marked by intense itching, and often accompanied by lesions on the oral mucosa

--------------------
"Few of us can do great things, but all of us can do small things with great love". Mother Theresa

http://www.facebook.com/profile.php?id=1629665573&ref=name

Posts: 938 | From Northeast Kingdom Vermont | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
scissorhappy
Junior Member
Member # 13183

Icon 1 posted      Profile for scissorhappy     Send New Private Message       Edit/Delete Post   Reply With Quote 
I would like to know the answer to that as well.
My dentist told me last month I had lichen planos in my mouth. Boy is it painful and annoying. I have symptoms of lymes but don't have a firm diagnosis. Had brain mri and showed
white matter that is consistant with ms. Right now besides the lichen planos, I have tingling, crawly, pins and needles feeling all up my legs, arms and hands. My western blot came back negative. In May I had what I thought was a mosquito bite that went into a large rash and looked like a circle. The rash didn't go away
for several weeks. I've just started reading on here hoping to educate myself so I can have control over my health. Thank you all for your wisdom. Any comments?

Posts: 6 | From northern calif | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
cmoc
Member
Member # 5135

Icon 1 posted      Profile for cmoc     Send New Private Message       Edit/Delete Post   Reply With Quote 
Is this in the same group as litchen sclerosis?

Chris

Posts: 22 | From England | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
scissorhappy
Junior Member
Member # 13183

Icon 1 posted      Profile for scissorhappy     Send New Private Message       Edit/Delete Post   Reply With Quote 
I believe they are in the same family.
Posts: 6 | From northern calif | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
cmoc
Member
Member # 5135

Icon 1 posted      Profile for cmoc     Send New Private Message       Edit/Delete Post   Reply With Quote 
I found this. I have litchen sclerosis.

Subject: lichen sclerosus et atrophicus / balanitis xerotica obliterans

source: Neuroborreliosis in morphea and lichen sclerosis et atrophicus
authors: Aberer, MD. et al.
Journal of the American Academy of Dermatolog; Volume 19--Number 5, Part 1
1988--pg. 820-825
"...Although there is no general agreement about the spirochetal origin of
morphea and lichen sclerosus et atrophicus, the isolation of Borrelia
organisms from one patient with morphea and the detection of spirochetes on histologic sections gives strong evidence that Borrelia can cause morphea and lichen sclerosis et atrophicus. We found significant antibodies to B. burgdorferi in 50% of patients with morphea and 45% of patients with lichen sclerosis et atrophicus. Of 179 dermatologic patients with various diagnoses, 11% displayed antibody titers ; 22% of Austrian recruits exposed to tick bites showed specific antibodies. Since 1949 morphea had been treated with penicillin which has resulted in frequent improvement of the course of the disease.
...High-dose penicillin therapy was administered to three patients and the progression of disease activity was stopped. At 1-year follow-up they remained free of recurrences.
"Eight of nine patients with morphea and two with lichen sclerosus et
atrophicus presented neurologic symptoms indicating that these diseases are
not only cutaneous but systemic diseases. The neurologic changes in morphea and lichen sclerosus et atrophicus correlate with the findings of stage II
neuroborreliosis similar to those in acrodermatitis chronica atrophicans.
This fact should encourage high-dose antibiotic therapy in both dermatoses, which was also proposed by Tuffanelli. The possibility of regeneration of the subepidermal nerve network after penicillin treatment also supports the need for antibiotic therapy.
"Our findings indicate involvement of the central and/or the peripheral
nervous system in patients with morphea and lichen sclerosus et atrophicus.
Because of the possible Borrelia origin of both diseases, the neurologic
symptoms should be regarded as central or peripheral neuroborreliosis. Thus
optimal antibiotic therapy should be tried in all types of morphea and lichen
sclerosus et atrophicus."

Chris

Posts: 22 | From England | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
scissorhappy
Junior Member
Member # 13183

Icon 10 posted      Profile for scissorhappy     Send New Private Message       Edit/Delete Post   Reply With Quote 
Chris,
Thank you for posting that info. I don't mean to sound stupid, my brain is only focusing on my tingling right now. Can you put this is more simple terms for me Please. Linda

Posts: 6 | From northern calif | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
cmoc
Member
Member # 5135

Icon 1 posted      Profile for cmoc     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sorry, really dizzy and tired today. I just cut and pasted it. I think it is saying that 40 or 50% of people that had litchen sclerosis had borrellia. Anyway, looks like there is a connection. Someone else might elaborate.

Best Wishes
Chris

Posts: 22 | From England | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
Ann in CA
LymeNet Contributor
Member # 97

Icon 1 posted      Profile for Ann in CA     Send New Private Message       Edit/Delete Post   Reply With Quote 
My dentist also thought that I possibly had lichen planus. Though it did not look like what the descriptions on line described. There was never any definite decision as to what it was, but it seems that it disappeared gradually after I started Theralac,

There may not have been any connection to starting the Theralac, but now it seems to be gone. My mouth had become very painful however, before Theralac, so when I realized it was gone, I credited Theralac.

Best wishes.

Ann

Posts: 287 | From Northern California, USA | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.