Polyarteritis nodosa is a form of vasculitis involving inflammation of medium-sized arteries.
Any organ can be affected but usually not the lungs.
Polyarteritis nodosa can be rapidly fatal or develop gradually.
Symptoms vary depending on which organ is affected.
Biopsy of an affected organ or arteriography of the blood vessels can confirm the diagnosis.
Prompt treatment with a corticosteroid, another medication that suppresses the immune system, or both is effective.
(See also Overview of Vasculitis.)
Polyarteritis nodosa most often develops during middle age, usually when people are in their 50s, but it can occur at any age. It is rare.
The cause of polyarteritis nodosa is unknown, but it sometimes appears to be triggered by certain viral infections (such as hepatitis B or in rare cases hepatitis C) or medications. About 20% of people with polyarteritis nodosa have hepatitis B or C. Some cases of polyarteritis nodosa has also been linked to a mutation in the adenosine deaminase 2 (ADA2) gene. Also, some people with a rare inflammatory condition called VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome caused by a mutation in the ubiquitin-like modifier-activating enzyme 1 (UBA1) gene have presented with polyarteritis nodosa. Medications may also cause the disorder, but most often no trigger can be identified.
The kidneys, skin, nerves, joints, muscles, and digestive tract are most commonly affected. The liver and heart are less often affected.
Symptoms of PAN
Polyarteritis nodosa can be mild at first but can worsen rapidly and be fatal within several months, or it can develop gradually as a chronic debilitating disease. Any organ or combination of organs can be affected. However, usually the lungs are not affected. Symptoms depend on which organs are affected and how severely they are affected. Occasionally, only one organ (such as the intestine) or a nerve is affected. At first, people may feel generally ill and tired and have a fever. They may lose their appetite and lose weight. Night sweats and generalized weakness are common symptoms.
Other symptoms occur when the arteries that carry blood to an organ are damaged, and the organ does not receive enough blood to function normally. Thus, symptoms vary depending on the organ that is affected:
Joints: Muscle pain, tenderness, and weakness; and joint pain (common) and joint inflammation (arthritis)
Kidneys: High blood pressure, blood in the urine, possible kidney failure with a buildup of toxic substances in the blood and decreased production of urine
Digestive tract: Severe pain, bloody diarrhea, nausea, vomiting, and tears (perforations) in the intestine
Heart: Chest pain (angina), heart attacks, and heart failure
Nerves: Patchy numbness, tingling, weakness, or paralysis in a hand or foot
Liver: Liver damage
Skin: Blue or red discoloration of the fingers or toes and occasionally skin sores
Genitals: Pain, tenderness, and inflammation in the testes (orchitis)
Sometimes damage to an organ is irreversible, and some or all of the organ function is lost. A weakened artery may rupture, causing internal bleeding. Problems, such as a heart attack, can occur long after the inflammation has been treated.
Diagnosis of PAN
A doctor's evaluation
Blood tests
Biopsy
Arteriography
Polyarteritis nodosa can be difficult to diagnose. Doctors suspect polyarteritis nodosa when people have a certain combination of symptoms and blood test results. For example, doctors may suspect the diagnosis if a previously healthy middle-aged person has various combinations of symptoms such as an unexplained fever, evidence of a certain pattern of nerve damage (such as difficulty raising a foot or bending the wrist), sores on the skin, pain in the abdomen or limbs, joint or muscle pain, or rapidly developing high blood pressure.
To confirm the diagnosis of polyarteritis nodosa, doctors may take a small sample of an affected organ and examine it under a microscope (biopsy) or take x-rays of the blood vessels (arteriography). For arteriography, images are recorded after a dye that is visible on x-rays (radiopaque contrast agent) is injected. Sometimes magnetic resonance angiography may be done to check for irregularities such as narrowing and dilations (aneurysms) in the wall of affected arteries. However, magnetic resonance angiography is less likely to confirm the diagnosis than angiography.
Doctors may do electromyography and nerve conduction studies to confirm nerve involvement and, sometimes, to help select the area for a muscle or nerve biopsy.
Treatment of PAN
Corticosteroids
Other immunosuppressants
Treatment of symptoms or underlying disorder as necessary
Treatment of polyarteritis nodosa is aimed at preventing damage from developing but often cannot reverse damage that has already occurred. Treatment depends on the severity of the disorder. Any medications that may have triggered the disorder are stopped.
If the corticosteroid does not reduce the inflammation adequately, medications that suppress the immune system
Other treatments, such as those used to control high blood pressure, are often needed to prevent damage to internal organs.
People who have hepatitis B are treated with corticosteroids and antiviral medications.
Prognosis for PAN
Without treatment, people with polyarteritis nodosa have a less than 15% chance of surviving 5 years. With treatment, people with polyarteritis nodosa have a greater than 80% chance of surviving 5 years. People whose kidneys, digestive tract, brain, or nerves are affected have a poor prognosis.
More Information
The following English-language resource may be useful. Please note that The Manual is not responsible for the content of this resource.
Vasculitis Foundation: About Polyarteritis Nodosa: Provides information for people with polyarteritis nodosa, including how to find a doctor, learn about research studies, and join patient advocacy groups
