Butterfly malar rash or stress rash?

New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

New Member

Date Joined Apr 2017
Total Posts : 2
   Posted 4/11/2017 7:08 PM (GMT -6)   
I have recently been receiving treatment for lupus due to a number of other symptoms and test results but I'm not sure if the rash I have is lupus related. It looks exactly like a malar rash however it comes on when I am stressed, nervous or embarrassed and generally lasts a few hours. Could this be a butterfly/malar rash? Thanks.

Post Edited (rachelshae) : 4/11/2017 7:11:37 PM (GMT-6)

Forum Moderator

Date Joined May 2005
Total Posts : 7674
   Posted 4/11/2017 7:26 PM (GMT -6)   
When we are stressed, our bodies react. For most people, it isn't a very visible or noticeable reaction, but when we have Lupus, reactions seem to be multiplied. Your rash probably is related to your Lupus.

As to whether it's "officially" a Malar rash - I couldn't say. I think that's mostly a matter of opinion, and even dermatologists and rheumatologists may disagree. I don't think the rash has to be permanent to be considered a Lupus rash.

Other than adding to the list of symptoms being used in initially diagnosing Lupus, I'm not sure how much it matters. I don't know of any treatments specifically for the rash.

My rash tends to always be visible on my arms, and only sometimes on my face.

Hope that helps!
Lynnwood, Lupus & Sjogren's Moderator, Dx: 2000
"Life is far too important to be taken seriously." - Oscar Wilde

New Member

Date Joined Apr 2017
Total Posts : 2
   Posted 4/12/2017 2:27 AM (GMT -6)   
Thanks Lynnwood, that helps!

Regular Member

Date Joined Oct 2016
Total Posts : 25
   Posted 4/12/2017 6:44 AM (GMT -6)   
When I get stressed or am flaring, I can usually feel the malar rash in the size and shape of a butterfly rash... however, it's never visible. I can feel my face burning and heating up in that shape, but when I look in the mirror there's nothing there!

Melissa D.
Regular Member

Date Joined Aug 2008
Total Posts : 434
   Posted 4/12/2017 11:08 AM (GMT -6)   
I would totally agree with the other ladies. When I was first diagnosed with lupus I had very little skin involvement, however, as time went on I began to notice if I was stressed or flaring. While lupus is so often linked to the butterfly or malar rash what many people don't realize is our disease can affect all of skin on all parts of our body. Lupus has definitely done that in my case anyway, I've literally had rashes or skin issues associated to my disease from head to toe.

Just be sure to discuss with your rheumatologist, if he/she feels it is something that can't be managed by your lupus medication they will refer you to a dermatologist.
Lupus SLE 1996, Sjogrens, Raynauds. My worst nightmare was imagined when my son was diagnosed with RA and Lupus NPSLE at 19.
New Topic Post Reply Printable Version
Forum Information
Currently it is Friday, March 23, 2018 11:06 AM (GMT -6)
There are a total of 2,943,126 posts in 322,921 threads.
View Active Threads

Who's Online
This forum has 161297 registered members. Please welcome our newest member, goldilocksNJ.
364 Guest(s), 6 Registered Member(s) are currently online.  Details
NicHostetler, Jasperilla, Michael_T, Dandrhuff, Scaredy Cat, ASAdvocate