PsA without inflamation?

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I am a 49 male and I have what I see as text book PsA symptoms for at least several years now. however, when I was finally referred to a Rheumatologist my blood work and x-rays show no inflamation therfore he has ruled out PsA in favor of OA. Despite having had sudden swelling in two fingers in the past along with SI joint (my syptoms started there 15/20 years ago). My psoriasis has only really developed in the last two years with small spots on mostly my legs, back of scalp, ears, elbows (first place) and lower back and now even genitals. I also have been in the E.R. three times over the last six years with chest pain/pressure which thankfully each time was not cardiac related, (I do have ongoing rib tenderness which seems to be related and most likley flared up mimicking cardiac symptoms ). Other strange symptoms that I have had, and seem to have progressed are: hearing loss with ringing in the ears, eyesight changes, dizzyness on standing, burning sensation on the top of my right foot, minor pitting and ridges of finger nails with edges that shred almost, thickening/yellowing of toe nails, finger joints ache constantly, Most painful is the hip joints and Sciatica causing usually my left leg to go numb to my foot. With all that said, I am just so frustrated that I feel my symptoms are all real and point to PsA but the test results so far do not. Anyone else have simlar symptoms and diagnosis? I Am not sure no where to turn as over the counter medications although work to some degree on the now 'normal' aches and pains, they do not for what I consider a 'flare' up (usually winter and early spring are the worst for flares), whicj also seem to be increasing, Any information this group can offer would be greatly appreciated as I need answers and some plan to try and relieve the constant paint and discomfort I have been having to live with for so long. I am still kind of young (lol) and my quality of life is suffering as well as my usually 'sunny' outlook on life! Am I honestly reading this all wrong being realted most likely to PsA?? Any words of wisdom would be welcome! Thank you!!

0 likes, 8 replies

8 Replies

  • Posted

    Hi Tim 

    you are showing all the signs of classic Arthritis but there are different form of it as you are aware. It took my GP two years to finally refer me to a specialist who diagnosed it as Psoratic Arthritis. My bloods show an increase in inflamation in the results and have gone from 20 when first diagnosed up to 32 at present even with medication but it can be a long road to finding the correct medication(s) for the individual. I really not sure what to suggest if the specialist is ruling PsA out apart from getting a second opinion. Some medications such as Ibrupen can cause problems with hearing. I am now 51 and my symptons starting showing over two years ago but not picked up on by my health proffessionals despite going back often with the same or different symptoms that all pointed to PsA so they can make mistakes and miss the real diagnoses. Personally i would keep a record of the pain and keep going to the GP for tests it was not until recently that i could see the inflamation in my joints but all the signs were there as the disease was attacking the joints with no physical signs but since it has show signs it got worse very quickly as the disease really took hold. There is proof that if caught within the first six months that a lot of damage to joints can be drastically reduced if treated correctly and blasted with high doses to stop or slow down its effects on the joints. 

    hope this helps 

    Rob 

  • Posted

    Hi Tim,

    sounds like PsA to me. Particularly when you mention nails. Keep a diary, including photographs and ask for a 2nd opinion. Good luck. Sheila

  • Posted

    Tim, your situation is almost identical to mine! I'm 47 and have been having strange symptoms for 15-20 years, including a sudden inflammation of my knee (around 2001) and itchy red patches on my skin that got brushed off as pityriasis rosea (1998), but was probably the first sign of psoriasis. And all through this time, I had increasing discomfort in my left sacroiliac joint and left knee and left foot. As in your case, X-rays and blood tests never showed much if any inflammation.

    Finally in 2014, the sacroiliac situation became severe, and that was followed by a big flare up of psoriasis and my doctor diagnosed it as PsA.

    He says one of the reasons for the lack of visible inflammation is that it's my tendons that are inflamed, not so much the joints themselves. It sounds like this is your case too. The rheumatic factor in your blood (the "deposits" they look for) are not a prerequisite for a PsA diagnosis, as far as I understand.

    I have never experienced the chest pains you describe, but interestingly, my brother has and his doctor says it's a rheumatic condition, so probably not surprising in your case.

    I also know the burning sensation you describe, also on top of my foot; I get dizzy on standing (my blood pressure tends to be low); have occasional tinnitus and have experienced the deterioration of my toenails (thankfully not my fingernails, yet) that you describe.

    I find it strange your doctor is not treating this as psoriatic arthritis. That said, my treatment (methotrexate + anti-inflammatory drug) has not been all that effective, but there is some relief available. The anti-inflammatory was especially effective on the crippling sacroiliac discomfort.

    It's terrible to feel this is all "in your head." It's not.

    Good luck getting your condition diagnosed and treated properly.

  • Posted

    Tim how awful for you

    I have PsA and as for the psoriasis part of it the only things I have to back that up are nails which are ridged and lift from the base and sausage fingers and toes. I nearly got diagnosed with RA as when I got the info back from my first visit with the rheumy I noticed in his notes that he had said no visible ridging in nails etc which I immediately wrote back to him and said he hadn't seen my nails and I had nail varnish on! On the second visit I was examined more thoroughly and diagnosed with PsA. I would go back and explain these symptoms which seem obvious to me and also get bloods done again. My inflammatory markers go up and down all the time so maybe you weren't having an 'attack'. It is sad but we have to fight for treatment in this field. Don't give up. Never stop smiling and in the meantime I find ice packs the best relief for pain. Good luck

    Lisa 😊

  • Posted

    Hi Tim I have had almost identical symptoms that you describe but for years no one put all of it together - I have been hospitalised twice with chest pain but discharged after 24 hours cause there was nothing wrong with my heart - thank goodness.  Three times now I have wakened up unable to get out of bed because every joint in my body hurt so much but again nothing in my blood work indicated rheumatoid arthritis so I kept it till it got better!!!  I was referred to rheumatology with suspected OA but after injections into my knee the consultant was going to discharge me as there was nothing else to be done - it was only when I mentioned I had tendonitis that she asked me if I had ever had psoriasis and I said yes in my 20's - she then said that expained the odd blood work results they had been getting and I was diagnosed with PA.  but here is the thing I have never been put in medication - just told to come back if I felt I needed another injection.  Since then I have had problems with my ankles, fingers toes shoulders as well as my knees.  Also had the yellowing of finger and toe nails.
    • Posted

      Hi Sylvester 

      reading the above you need to get a proper diagnoses clearly you have PsA. Dont be fobbed off and get the treatment the longer this goes on the more damage will be caused which can not be reversed. If you have to insist you see a specialist and or get a second opinion 

       

    • Posted

      Thank you Robert - I have also in the last year been diagnosed with paroxysmal atrial fibrilation - did a bit of research and there is a thought the two could be related - to be honest I am really scared to take any other kind of mediction because of the PAF. This includes pain relief which makes flare ups really uncomfortable!!
  • Posted

    Hi again Tim

    the inflammatory marker blood test for RA is either positive or negative. Even 20% of folk with RA have a negative reading. This group of people with the negative blood marker are referred to seronegative arthritis, of which PsA is one. The difficulty in diagnosing this is there is no one simple test! But a selection of some of the following usually leads to a diagnosis:

    Psoriasis usually (but not always precedes PsA, usually 5-10yr)

    sausage toes and fingers

    pitting, yellowing and lifting of nails

    fatigue

    stiffness, particularly am

    swelling and pain, any joint, usually mirrored on the other side

    this is not a complete list, look at PAPAA or Arthritis Research websites for more info.

    finally, getting that 2nd opinion. Early treatment is needed to limit joint damage. Let us know how you getting on. Sheila x

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