Wegener�s granulomatosisDefinition: Wegener's granulomatosis is a rare disorder�that causes�blood vessels in the upper respiratory tract (nose, sinuses, ears), lungs, and kidneys to become swollen and inflammed. The eyes, skin, and joints�may also be affected. Arthritis occurs in�about half of all cases.
Alternative Names: Midline granulomatosis
Causes, incidence, and risk factors: The cause is unknown.�Wegener's granulomatosis is thought to be an autoimmune disorder. Patients with this disease develop sores (lesions) in the�respiratory tract and the kidneys.�Kidney lesions cause glomerulonephritis, which�may result in blood in the urine and kidney failure. Kidney disease can quickly get worse.�If untreated, kidney failure and death occur in more than 90% of patients. Wegener's granulomatosis is most common in middle-aged adults. Men are affected twice as often as women. It is rare in children, but has been seen in infants as young as 3 months old.
Symptoms: Frequent sinusitis is the most common symptom. Other early symptoms include persistent fever without an obvious cause,�night sweats, fatigue, and� malaise (an ill feeling). Chronic ear infections�may also�come before�the diagnosis of Wegener's granulomatosis. Other upper respiratory symptoms include nose bleeds, pain, and sores around the opening of the nose. Loss of appetite and weight loss are common. Skin lesions typically occur, but there is no one�typical lesion associated with the disease. Symptoms of kidney disease may be present (but not always). The urine may be bloody, and often first appears as red or smoky urine. Eye problems develop in a significant number of patients. They�may range from mild conjunctivitis to severe�swelling of the eye. Other symptoms include:
Signs and tests: A variety of tests may be performed, including: - Biopsy of abnormal tissue:
- Urinalysis to look for signs of kidney disease such as protein and blood in the urine.� The presence of kidney disease is necessary to make a definitive diagnosis of Wegener's granulomatosis.
- Chest x-ray �
- Bone marrow aspiration
- Blood tests to look for antibodies that the body makes against its own tissue.
Treatment: Treatment with corticosteroids, cyclophosphamide, methotrexate, or azathioprine produces long-term remission in over 90% of patients.
Support Groups: Support groups with others who suffer from similar diseases may help patients and their families learn about their diseases and adjust to the changes associated with the treatment.
Expectations (prognosis): With treatment, most people recover within months. However, some may develop chronic renal failure. Without treatment, patients can die within a few months. �
Complications: Complications usually result from lack of treatment. - Chronic kidney failure
- Hemoptysis (coughing up blood)
- Respiratory failure
- Inflammation of the eyes
- Nasal septum perforation (hole inside the nose)
- Rash
Medications used to treat the disease can cause side effects, which may also lead to complications.
Calling your health care provider: Call your health care provider if chest pain, coughing up blood, blood in the urine, or other symptoms of this disorder are present.
Prevention: No preventive measures are known.
References: Murray J, Nadel J. Textbook of Respiratory Medicine. 3rd ed. Philadelphia, Pa: W.B. Saunders Company; 2000: 1462-1463.
| 
