Comment from: JLB, 45-54 Female (Patient)Published: May 05
I am a 53-year-old female that has been diagnosed with vasculitis (PAN). I was referred to a rheumatologist and am on prednisone and methotrexate, probably for two years. My symptoms were lesions on my legs, Reynaud's syndrome in my fingers and toes, fevers, muscle and joint pain, and fatigue. My doctor says the longer I am on treatment, the better my chances are for a long-term remission. I spent 10 months with one doctor before I tried an internist, who suggested right away that it might be vasculitis. I am grateful for the quick diagnosis.
Comment from: harry, 55-64 Male (Patient)Published: May 05
My father has vasculitis, but it is not clear exactly what type he has. His case has been ambiguous from the start. He was a typically healthy adult male, but that changed two years ago. His condition began with tingling in his fingers to burning on the bottom of his feet. As time progressed, nodules were found in his lungs. After subsequent tests/operations, such as an open lung biopsy and needle biopsy, he was diagnosed. (The biopsies came out non-specific so the doctors deemed the nodules irrelevant to the disease as a whole). On the bright side, his organs have not been affected by this disease. As of right now, he is no longer in the hospital, but he still has some of his old problems. He is still disabled despite continued physical therapy and medicine (although he stopped the cyclosporin in August after discovering it was adversely affecting his kidneys).
Comment from: Lady369, 35-44 Female (Patient)Published: April 27
I am a 40 year old single mother of three. I was diagnosed with Vasculitis more than a year ago. I was 36 years old when my symptoms first started. At first I thought I had two small pimples inside my nostrils. During the night, I woke up to a swollen nose. When the sun came up, any kind of light hurt my head. I was sluggish and achy all over. I went to the hospital and they gave me some medication to fight, what they called, an infection in my nose. Over the course of three days, my condition worsened. I couldn't walk without assistance, I couldn't open my eyes nor could I smell anything. Another three or four days passed, the glands under each armpit were so inflamed I couldn't put my arms down. My head hurt so bad I had to be taken to the hospital. In a matter of 10 days, I was in the hospital have CT Scans, MRIs, blood draws and a spinal tap. I was misdiagnosed five times at first. After the hospital visit, I was no longer able to use my legs. My son had to help me up and down the stairs and in and out of the bathtub. My legs had given out on me that I ended up using a walker for four months. No one could figure it out. I went to a number of specialists until I finally was referred to a rheumatologist. I go every six months now. It's been a rough time for me, but actually I forgot I was diagnosed with the disease. I guess I was in denial. I've been feeling sluggish and feverish; can barely get up to go to work some mornings. I just thought I wasn't getting enough rest because I travel so much. Well, I've also been under a lot of stress. My rheumatologists told me my symptoms of me being tired lately is because of the vasculitis. Only my left leg hurts, or feels restless most times. My ankle swells up and I started seeing small bruises show up on my legs. I guess since I'm new to this, I would love to find out is there a cure for this disease.
Comment from: Gina, 35-44 Female (Patient)Published: April 23
I have got Vasculitis (Henoch-Purpura Schonlein). For nearly a year now it started of with a bite on my foot which got a lot of blisters, then the rash increased to my legs, arms, face and so on. My legs were swollen and sore. My husband had to take me to the Hospital because of the pain. I was under one Doctor who was no use so again my Husband looked for a second opinion. This time a Doctor who understood what I have. I had been on the Prednisone and other high doses of Medication and have very bad side effects, blue hands, fingers mouth. This is not good. This condition has affected my kidneys, and I get bad headaches. At this point now my doctor does not know when or if this will ever go away. She thinks I could have this forever, as normally it is only a short term condition. Even now I still get outbreaks on my legs, arms, and my legs itch so bad. The Doctors think that my Vasculitis was caused by a virus not the bite.
Comment from: stevs, 45-54 Male (Patient)Published: March 23
My problem started as a tingling of the toes. As six months went by, the pain increased monthly until it felt like someone had poured gasoline on my feet. My doctor had no idea what the problem was. I went to a neuroscience institute where they gave me a biopsy of the calf muscle and foot nerve. It came back as positive for vasculitis. I took 12 months of cytoxin and prednisone. These lessened the pain, but the pain never went away totally in my feet. A second biopsy determined the vasculitis was in remission. I was finally weaned off the prednisone after two years, but I'm still taking oxycontin and gabapentin, which only take the edge off the pain. They now continue to look for ways to stop the pain, but I'm so tired of the constant pain in my feet.
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Rheumatoid arthritis is an autoimmune disease that causes chronic inflammation of the joints, the tissue around the joints, as well as other organs in the body. Because it can affect multiple other organs of the body, rheumatoid arthritis is referred to as a systemic illness and is sometimes called rheumatoid disease.
Sjögren's syndrome is an autoimmune disease involving the abnormal production of extra antibodies that attack the glands and connective tissue. Sjögren's syndrome with gland inflammation (resulting dry eyes and mouth, etc.) that is not associated with another connective tissue disease is referred to as primary Sjögren's syndrome. Sjögren's syndrome that is also associated with a connective tissue disease, such as rheumatoid arthritis, systemic lupus erythematosus, or scleroderma, is referred to as secondary Sjögren's syndrome. Though there is no cure for Sjögren's syndrome, the symptoms may be treated by using lubricating eye ointments, drinking plenty of water, humidifying the air, and using glycerin swabs. Medications are also available to treat dry eye and dry mouth.
Systemic lupus erythematosus is a condition characterized by chronic inflammation of body tissues caused by autoimmune disease. Lupus can cause disease of the skin, heart, lungs, kidneys, joints, and nervous
system. When only the skin is involved, the condition is called discoid lupus.
When internal organs are involved, the condition is called systemic lupus
erythematosus (SLE).
Hepatitis C is an inflammation of the liver due to the hepatitis C virus (HCV), which is usually spread by
blood transfusion, hemodialysis, and needle sticks, especially with intravenous
drug abuse. Chronic hepatitis C may be treated with interferon, usually in combination with anti-virals.
Dementia is a significant loss of intellectual abilities such as memory capacity, severe enough to interfere with social or occupational functioning. There are different criteria classification schemes for dementias such as cortical, subcortical, progressive, primary, and secondary dementias. Other conditions and medication reactions can also cause dementia. Dementia is diagnosed based on a certain set of criteria. Treatment for dementia is generally focused on the symptoms of the disease.
The hepatitis B virus is a unique, coated DNA virus belonging to the Hepadnaviridae family of viruses. The course of the virus is determined primarily by the age at which the infection is acquired and the interaction between the virus and the body's immune system. Successful treatment is associated with a reduction in liver injury and fibrosis (scarring), a decreased likelihood of developing cirrhosis and its complications, including liver cancer, and a prolonged survival.
Thrombocytopenia refers to a decreased number of platelets in the blood. There are many causes of thrombocytopenia such as decreased platelet production (viral infections for example rubella, mumps, chickenpox, hepatitis C, and HIV); increased platelet destruction or consumption (for example sulfonamide antibiotics, heparin, blood transfusions, and lupus); or increased splenic sequestration (enlarged spleen due to conditions for example liver disease, blood cancers, and more). Treatment of thrombocytopenia depends on the cause.
Henoch-Schonlein Purpura (HSP or anaphylactoid purpura), a type of blood vessel inflammation, results in rash, arthritis, and occasional abdominal cramping. HSP often resolves on its own. Joint pain may be treated with anti-inflammatory and cortisone medications.
Polymyalgia rheumatica (PMR) is a disorder of the muscles and joints that causes pain and stiffness in the arms, neck, shoulders, and buttocks. Treatment for polymyalgia rheumatica aims to reduce inflammation with aspirin, ibuprofen and low doses of cortisone medications. Giant cell arteritis, inflammation of blood vessel walls, affects 10-15 percent of polymyalgia rheumatica patients. Symptoms of giant cell arteritis include fatigue, weight loss, low-grade fever, jaw pain when chewing, scalp tenderness, and headaches. High doses of cortisone medications are used to treat giant cell arteritis.
Kawasaki disease is a rare children's disease characterized by a fever that lasts more than five days and at least four of the following five symptoms are present: rash, swollen neck lymph gland, red tongue, swelling or redness of the hands or feet, and conjunctivitis. High doses of aspirin are used to treat Kawasaki disease. Cortisone and antiinflammatory drugs may also be used during treatment.
Wegener's granulomatosis, a condition that usually affects young or middle-aged adults, is an inflammation of the arteries supplying blood to the sinuses, lungs, and kidneys. Symptoms of Wegener's granulomatosis include bloody sputum, fatigue, weight loss, joint pain, sinusitis, shortness of breath, and fever. Wegener's granulomatosis may be fatal within months without treatment. Treatment aims to stop inflammation with high doses of prednisone and cyclophosphamide.
Renal artery stenosis is a narrowing of the diameter of the renal arteries. When the renal arteries narrow, the result is restricted blood flow to the kidneys, which may lead to impaired kidney function and high blood pressure (referred to as renovascular hypertension (RVHT). Renal artery stenosis can occur in one or both kidneys. The primary cause of renal artery stenosis is atherosclerosis. Risk factors for renal artery stenosis include high blood pressure, high cholesterol levels, age, cigarette smoking, and diabetes. Symptoms of renal artery stenosis include high blood pressure that does not respond to treatment, severe high blood pressure in individuals younger than 30 or greater than 50 years of age. Renal artery stenosis is diagnosed with imaging and functional tests. Treatment for renal artery stenosis include medication or surgery.
Behcet's syndrome is a disease characterized by three symptoms: genital ulcers, recurring mouth ulcers, and inflammation around the pupil of the eye. Symptoms of Behcet's syndrome may also include inflammation of other areas of the body, such as the brain, joints, skin, retina, and bowels. Oral steroids, antiinflammatory drugs, and steroid gels, pastes, and creams may be used to treat Behcet's syndrome.
Relapsing polychondritis is an uncommon, chronic disorder of the cartilage that is characterized by recurrent episodes of inflammation of the cartilage of various tissues of the body. Tissues containing cartilage that can become inflamed include the ears, nose, joints, spine, and windpipe (trachea). Tissues that have a biochemical makeup similar to that of cartilage such as the eyes, heart, and blood vessels, can also be affected. Nonsteroidal antiinflammatory medications (NSAIDs) is used as treatment for mild cases of the disease. Steroid-related medications also are usually required.
Churg-Strauss Syndrome is a form of vasculitis. Vasculitis is an inflammation of the blood vessels. Symptoms of Churg-Strauss syndrome include fatigue, weight loss, inflammation of the nasal passages, numbness, and weakness. Treatment is directed toward both quieting the vasculitis and suppressing the immune system.
Takayasu disease (also referred to as Takayasu arteritis) is a chronic inflammation of the aorta and it's branch arteries. Takayasu disease is most common of Women of Asian descent and usually begins between 10 and 30 years of age. Symptoms include: painful extremities, dizziness, headaches, chest and abdominal pain, and a low-grade fever. Treatment for Takayasu disease includes cortisone medication to suppress the inflammation.
Polyarteritis nodosa is a rare autoimmune disease characterized by spontaneous inflammation of the arteries of the body. The most common areas of involvement include the muscles, joints, intestines (bowels), nerves, kidneys, and skin. Poor function or pain in any of these organs can be a symptom. Polyarteritis nodosa is most common in middle age persons. Polyarteritis is a serious illness that can be fatal. Treatment is focused on decreasing the inflammation of the arteries by suppressing the immune system.
Severe acute respiratory syndrome (SARS) is a respiratory disease caused by the coronavirus SARS-CoV. Symptoms include fever and shortness of breath. Patients with SARS often require oxygen and severe cases require mechanical ventilation.
Essential mixed cryoglobulinemia is a condition caused by abnormal blood proteins called cryoglobulins. Symptoms include joint pain, swelling, skin vasculitis, enlarged spleen, and nerve and kidney disease. Treatment involves medications that reduce inflammation and suppress the immune system.
Kawasaki's disease is an uncommon illness in children that is
characterized by high fever of at least five days' duration together with
at least four of the
following five findings:
Inflammation with reddening of the whites of the eyes (conjunctivitis) without pus
Redness or swelling of the hands or feet, or generalized skin peeling
Rash
Lymph node swelling in the neck
Cracking inflamed lips or throat, or red "strawberry" tongue
The above criteria are used to make a diagnosis of Kawasaki's disease. The terminology "incomplete Kawasaki's disease" is sometimes used for patients with only some features of classical Kawasaki's disease.
What is mucocutaneous lymph node syndrome?
Mucocutaneous lymph node syndrome is the original name for Kawasaki's disease. The original name was quite descriptive because the disease ...
I am a 53-year-old female that has been diagnosed with vasculitis (PAN). I was referred to a rheumatologist and am on prednisone and methotrexate, probably for two years. My symptoms were lesions on my legs, Reynaud's syndrome in my fingers and toes, fevers, muscle and joint pain, and fatigue. My doctor says the longer I am on treatment, the better my chances are for a long-term remission. I spent 10 months with one doctor before I tried an internist, who suggested right away that it might be vasculitis. I am grateful for the quick diagnosis.
Related Reading: vasculitis | prednisone | methotrexate