Chronic Necrotizing Vasculitis

Below you will find more information about Chronic Necrotizing Vasculitis from Medigest. If you believe that you are suffering from any of the symptoms of Chronic Necrotizing Vasculitis it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Chronic Necrotizing Vasculitis and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Chronic Necrotizing Vasculitis comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Chronic necrotizing vasculitis is the destruction and inflammation of "blood vessel walls", leading to termination of the related tissue.


A physician will do a physical examination. Neurological exam can show indications of the nerve damage. Tests that can be done include biopsy, sedimentation rate, chest X-ray, urinalysis, antibodies blood test against neutrophils, and hepatitis blood test.


Low doses of Corticosteroids or a different medication that suppresses a patient's immune system can reduce blood vessel inflammation.

Symptoms and Signs

Signs of the condition are determined through the location and extent of the inflammation. This inflammation likely has an autoimmune origin. Common symptoms include skin lesions that are purple or red in color, papule, and located on hands, legs, or other parts; a change in color of the fingers, such as blue toes or fingers; tissue death because of deficient oxygen, tenderness or pain in the region, ulcers that don't heal, skin redness; abdominal pain; joint pain; numbness or tingling in leg, arm, and other area; fever; and decrease or change in the function of a leg, arm, or other body part.


Chronic necrotizing vasculitis can come about in rheumatoid arthritis, and usually noticed with sclerroderma, polyarteritis nodosa, and systematic lupus erythematosus. The inflammation's cause is not known, but is possibly connected to some autoimmune factors.

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