Sudden haematomas with no reason?: Hello, Lately I... - LUPUS UK

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Sudden haematomas with no reason?

wiselyfair profile image
9 Replies

Hello,

Lately I started having sharp pains of a couple of seconds in my legs followed by pretty nasty bruises/haematomas. First I thought it was a bruise due to bumping into something I did not remember, but now it is becoming more frequent.

Anyone experiencing the same or similar?

Many thanks

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wiselyfair profile image
wiselyfair
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9 Replies
gemim profile image
gemim

Hello wiselyfair,

For the last few days I have been having exactly the same problem - really sharp shooting pain in my foot and then a haematoma appeared out of nowhere on my shin. Never had either before. Diagnosed with SLE. Raynaud’s & Sjogrën’s 25 years ago with Sjogrën’s flare up a couple of years ago. Look forward to hearing if others can shed any light on the cause and/or prevention of this.

Gemim

Olive12345 profile image
Olive12345

I get these too! I went through a patch where they were really frequent but haven’t had one in a while now. Not sure what I’ve done differently though to make them stop.

Star13 profile image
Star13

Anyone with Lupus should be tested for The antibodies for APS as around a third of people will have them. If that’s the case you may need to take something like a baby aspirin daily but I’d discuss this with your Dr as is the case with any new symptom.

tiredmum profile image
tiredmum

I get this too but on my feet. Sharp pain that lasts a few minutes and then bam a massive black bruise but no more pain .

I have APS too. I showed my GP it once and she wasn’t phased at all.

Get tested for APS .

4373 profile image
4373 in reply to tiredmum

What’s APS?

Poshcards profile image
Poshcards in reply to 4373

anti physfoid syndrome sorry not sure of spelling x

Star13 profile image
Star13 in reply to 4373

Antiphospholipid Syndrome

tiredmum profile image
tiredmum

anti phospholipid syndrome or Hughes syndrome .

Lily77 profile image
Lily77

Yes just as Tiredmum says named after Professor Hughes based at the London Lupus Centre. I have met him!

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