Facial Rash

[barrypalmerbkp]

Hi, I have been diagnosed with Lupus after having a biopsy done on my face due to a facial rash. Would anyone be able tell me the name of the rash please?

Many Thanks

[Spanielmadlady]

malar rash is the name of the facial rash associated with lupus.stay out of the sun,cover up head to toe with clothes,sun cream,hat and sunglasses all year.skin expose to the sun anywhere on the body will trigger a rash in your usual place

[nanleighh]

Hi. It could be malar rash or it could be a type of lupus that just affects your skin. Either way as spanielmalady says you need to be careful with the sun. Hopefully your doctor will do appropriate tests to see if your lupus is systemic or not. The treatment varies depending on the type of lupus you have. Hopefully you have been sent to a rheumatologist for further testing and treatment. If systemic lupus you would have other symptoms such as joint pain, hair loss, fatigue, and/or a combination of other symptoms. I am glad you found this forum. There are very wise and experienced caring people on here. I wish you the best. X Nan

[Frosty1960]

Not that uncommon had the same biopsy from my forehead to get diagnosis.

[lupie46]

Lupus erythematosus rash or discoid Malar rash....

[Chanpreet_Walia LUPUS UK]

Hi Barrypalmerbkp,

Welcome to the LUPUS UK HealthUnlocked forum. We offer a free information pack which you can request at lupusuk.org.uk/request-info....

A malar (butterfly) rash is commonly associated with lupus. The rash is usually a pink or reddish-coloured rash that mainly occurs on the cheeks and the bridge of the nose. It can sometimes appear on the forehead, chin and chest of some people with lupus.

A malar rash is generally not permanent; it often appears when disease activity is higher (during a flare) or when exposed to certain triggers such as UV light. To find out how rashes can be treated, you can read our booklet on lupus and the skin here: lupusuk.org.uk/wp-content/u...

For tips and information on coping with light sensitivity visit lupusuk.org.uk/coping-with-....

Best wishes,

Chanpreet

[Pegy]

I suffer from this, at times it can cover all parts of my body, with me it blisters, weeps & sometimes bleed. I always cover myself head to toe with hat, scarf, long sleeves & loosely fitted tops/ dresses, topped off with leggings. Factor 50 sunblock can be prescribed by your consultant/gp. With my lupus I’m prescribed steroid cream to alleviate pain, however be careful as this can have an adverse effect. My skin is quite scared from all the skin flares. Xx