Vasculitis means inflammation of blood vessels.
The effects of vasculitis depend on the sizes of the blood vessels
that are affected and on the parts of the body involved. Commonly
vasculitis may only affect the skin (cutaneous vasculitis, as
shown in the picture). Sometimes it affects many organs at the
same time (systemic vasculitis). There are many varieties of systemic
vasculitis, and they are often given peculiar and difficult names
. However it is useful to know the variety as the treatment may
differ, and some types are more likely to come back again. Some
types of systemic vasculitis commonly start by affecting a single
organ, for example, the kidney.
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What causes vasculitis? |
| Symptoms of vasculitis | |
| How is vasculitis diagnosed? | |
| What types of vasculitis affect the kidney? | |
| Will I need dialysis? | |
| What are ANCA? | |
| Further information |
Usually the cause of vasculitis is unknown. Sometimes it occurs as an allergic reaction, for example, to medication. Vasculitis is not a hereditary disease and it does not run in families. Some types may be caused by infections, for instance with hepatitis viruses and some bacteria.
Cutaneous vasculitis causes a skin rash
(see the picture above) and sometimes pain. Systemic vasculitis
commonly causes general symptoms such as feeling unwell, weight
loss, night sweats and joint pains. Sometimes it may come on very
suddenly and dramatically, but it commonly comes on gradually
over days and weeks.
Any organ may be affected by vasculitis. When it affects the kidney,
blood and protein may appear in the urine, but this may only be
shown by urine testing. Kidney failure does not produce many symptoms
until a lot of damage has occurred. Disease in the lungs may cause
breathlessness and a cough, and occasionally bleeding causes the
patient to cough up blood. Weakness and numbness of the hands
and feet may be caused by inflammation of tiny blood vessels supplying
nerves. Abdominal pain and bleeding may be caused by vasculitis
in the gut, and occasionally this may lead to severe bleeding
or to bowel perforation. Vasculitis in the heart may result in
symptoms similar to a heart attack, and in the brain it may cause
confusion, symptoms of a stroke or fits.
When vasculitis comes on slowly it is almost inevitable that correct diagnosis is delayed, as its early symptoms closely resemble influenza or other infections or illnesses. Routine blood tests are also rarely very abnormal early on. Anaemia is common, and there may be signs that suggest infection or inflammation. In some types of severe vasculitis, ANCA tests (described below) may help, although they do not prove the diagnosis on their own. Examination of a sample from an affected part of the body under the microscope is often required to confirm the diagnosis. Kidney biopsies are particularly helpful if there are signs of kidney involvement. Special x-rays (angiograms) can sometimes diagnose vasculitis affecting large blood vessels.
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Vasculitis and vessels affected |
The kidney is particularly likely to be
affected by small vessel vasculitis (SVV) which may involve the
tiny blood vessels in the filtering units of the kidney. Inflammation
of these filters is called glomerulonephritis. It is a common
cause of a severe but treatable kidney disease called crescentic
nephritis, because of the appearance under the microscope.
This is also called rapidly progressive glomerulonephritis (RPGN)
because of the speed with which it can cause kidney failure.
SVV affecting the kidney is usually caused by one of two types
of vasculitis, microscopic polyangiitis (MPA) and Wegener's
disease. The appearances of these two diseases in the kidney
are usually identical, but disease affecting other organs may
help to tell them apart. ANCA may help with the diagnosis of SVV.
Treatment of severe kidney disease is identical in either case.
Some types of vasculitis are described further
in the table at the foot of this
page.
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In severe SVV, it is common for dialysis to be required soon after the diagnosis is made. However treatment can often heal severe kidney disease, so that dialysis is no longer required, even where some scarring and kidney damage remains.
Antibodies are molecules that are found in the blood stream. They are mainly there to fight infections by targeting foreign molecules. ANCA (anti-neutrophil cytoplasmic antibodies) stick to molecules found in white blood cells rather than to foreign material. These antibodies are often found in the blood of patients with small vessel vasculitis (SVV). It is not clear whether ANCA cause vasculitis, but they can be very helpful in the diagnosis. Unfortunately similar antibodies may be found in other diseases, and not all vasculitis may be ANCA positive, so the test is not 100% reliable as a way of making a diagnosis.
Severe types of systemic vasculitis often require powerful treatments to suppress the inflammation and the powerful immune response. Treatments may include Steroids, Cyclophosphamide, Azathioprine, Plasma exchange, and other drugs. If vasculitis is due to an infection, treatment for the infection is important.
This article was used as the basis of 'What we tell our patients about vasculitis', published in the British Journal of Renal Medicine in Summer 2000 (Vol. 5 pages 13-16).
| John Hopkins Vasculitis Centre | A very detailed web site, which gives in depth explanations; the illustrations however are quite graphic. |
| CSSIG | Go to Frequently Asked Questions at the Churg Strauss International Support Group site for a relatively straightforward description of important questions about this type of vasculitis |
| Other vasculitis web pages | From EUVAS, the European Vasculitis Study Group |
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Types of Vasculitis
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Disease |
Blood vessels affected |
Remarks |
| Takayasu's
disease, (Pulseless disease) |
Large | Mainly young women from the far east are affected, resulting in a long disease, treatment is difficult |
| Kawasaki disease | Large | Children are affected possibly after an infection. Heart arteries are especially affected. Steroid treatment is harmful. Responds to IVIG |
| Polyarteritis nodosa (PAN) | Medium | Rare, but quite well known as it was the earliest vasculitis to be recognised. |
| Temporal
arteritis (Giant cell arteritis) |
Medium | Common disease of over 60's that causes headache and general illness, sometimes with other symptoms. Responds to steroids alone. |
| Churg-Strauss syndrome | Medium/Small | Disease of over 50's often with late onset asthma. Particularly affects lung, and nerves to arms and legs. ANCA usually present. |
| Microscopic Polyarteritis (MPA) | Small | Affects all ages but more common in elderly. Kidneys, skin and gut affected. ANCA usually present. |
| Wegener's granulomatosis | Small | All ages and similar to MPA, but may also cause a slower longer inflammation also affecting nose, sinuses and lungs. ANCA is useful. |
| Henoch - Schonlein Purpura | Small | Common in children, who usually get a rash, abdominal pain (gut vasculitis) and mild kidney involvement. Often more severe when it occurs in adults. ANCA negative |
This
information is published from the Renal Unit at the Royal Infirmary
of Edinburgh, Scotland, UK, Renal@ed.ac.uk The author of this page was Gemma Browne. It was first published in April 2000 and last updated
Please be aware that while we have made all efforts to ensure that this information is accurate, we cannot guarantee that there are no mistakes. Also that the best management for individual patients may differ from that outlined here. Only the doctors caring for the patient will be able to advise on this.
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