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could members please share with me, the symptoms of great cell artery inflammation. i know it is supposed to cause pain, but where, how much, how often. and how is it diagnosed, and how is it treated.  thanks in advance...............i am at 4.5 mgm prednisone, but cant get any lower at the moment. < ="-" ="text/; =utf-8">< name="ProgId" ="Word.">< name="Generator" ="Microsoft Word 9">< name="Originator" ="Microsoft Word 9"><>

Giant Cell Arteritis (Temporal Arteritis)

The main early symptoms of giant cell arteritis are headache and tenderness over the sides of the forehead. People with giant cell arteritis need urgent treatment with steroids. Treatment will usually prevent serious complications such as eye problems and blindness.

What is giant cell arteritis and who does it affect?

Giant cell arteritis is a condition which causes inflammation on the inside of some arteries (blood vessels). It is called 'giant cell' because abnormal large cells develop in the wall of the inflamed arteries. The arteries commonly affected are those around the head and neck area. The artery most commonly affected is the temporal artery. (You have a temporal artery on each side of the head. They are under the skin to the sides of the forehead - the temple area.) Therefore, the condition is sometimes called 'temporal arteritis'.

Giant cell arteritis is uncommon and mainly affects people over the age of 60. It rarely affects people under 50. Women are more commonly affected than men. The cause is not known.

What are the symptoms of giant cell arteritis?

Up to half of people with giant cell arteritis develop a related condition at the same time called polymyalgia rheumatica. If this develops you will also develop pain, tenderness and stiffness of muscles around the shoulders, hips and back.  The treatment is similar for both conditions.

What are the possible complications of giant cell arteritis?

Complications are much less likely to occur if treatment is started soon after symptoms begin. Possible complications of untreated giant cell arteritis include the following.

Do I need any tests?

A blood test can detect if there is inflammation in your body. If the blood test shows a high level of inflammation, and you have the typical symptoms, then giant cell arteritis is likely. However, the blood test is not specific for giant cell arteritis (it can also be high in other 'inflammatory disorders'.) Also, some people with giant cell arteritis have a normal blood test.

To confirm the diagnosis a doctor may take a small part of the temporal artery (a biopsy) to look at under a microscope. If you have giant cell arteritis a doctor can see the inflammation and abnormal giant cells in the sample of the artery wall.

Treatment is usually starts with a high dose of  Prednisolone (cocosteroids) 40-60 mg then a slow drop down.  Relapses can occur.  Some GCA patients are treated with Methotextrate (chemo based).

GCA is not to be messed around with - We more information on diagnoses and treatment.
If  you want more information, please email pmrfighters@yahoo.co.uk and also tell us if you are on broadband. 

mrs UK


Mrs UK has posted the most accurate information - follow what she's said. 
As a GCA/Temporal Arteritis/PMR patient I have only a few things to add:

1. My headaches felt like someone was tightening a hatband around my head, and it was impossible to chew or even bite anything crisp (like an apple or celery) because of the pain in my jaw joints.

2. The fatigue and lack of stamina, combined with the pain, left me feeling like a zombie for over a year.  That can lead to major bouts of depression (and the Prednisone doesn't help that).  Eventually, with proper treatment and passage of time, it will ease off.

3. I had temporal biopsies on both sides and they were negative.  However, that does not totally rule out GCA.  Studies show (sorry, I don't have the citations) that 5% of GCA biopsies will be negative.  Then the only diagnostic evidence is the ongoing symptoms and positive response to Prednisone.  It requires constant monitoring (I've been seeing a rheumatologist monthly for two years, and I'm still not out of the woods)

Best wishes to you.  It can be a multi-year battle, and sometimes it can get depressing.  Hang in, the symptoms will slowly ease off.

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