Discussions By Condition: Autoimmune Disease

C Reactive Protein of 66.8 in my 6year old!!!!

Posted In: Autoimmune Disease 1 Replies
  • Posted By: beckieeric07
  • December 1, 2010
  • 05:47 PM

My 6 year old daughters symptoms started 2 months ago. I started to notice her getting very cranky at night, so just for the heck of it one night I took her temp even though she didn't feel that warm. It was very low grade. I wasn't worried at first until it started happening every night and only at night. Then she started complaining of a sore throat so I took her to her pedi. She had a round of normal bloodwork and throat culture, that all came out fine. About a month later, still with on going nightly fevers, she started developing a rash all over. I called the pedi who recommended benydryl. We both thought she was just having a mild allergic reaction to something. But then the rash started coming almost like clockwork with the fevers. She also started complaining of upper abdomen pain . I took her back to the pedi who ran another round of bloodwork, a little more extensive this time. She tested neg for Lyme, Mono, and EBV. Her white count came back slightly elevated at 17,000. Most concerning was her C reactive Protein rate of 66.8. A few other minor elevations with monocytes and LDH. However her sed rate and Rheumatoid factors all came out normal. Her fevers are only "low grade" (99.5-100.7) but to me, when my daughter is cranky and lethargic during them and absolutely fine when it goes down, they are fevers. I don't know where else to turn. They know there is severe inflammation somewhere but don't know from were and are reluctant to run any more tests because she's not symptomatic 24/7

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  • I hope that by now the problem has been fixed or at least diagnosed but if it hasn't here is some info of a disease that is not often thought of until problems have gone on for years. Many of us that have it get treated like hypochondriacs until we do the research on our own as it is not a very common illness. I hope this info is helpful to you feel free to message me back to let me know or if you have any questions I would be more then happy to help. MOST COMMON SYMPTOMS AND SIGNSOF BEHCET'S DISEASEBehcet's Disease is common in the Middle East, Asia, and Japan. It is rare in the United States. In Middle Eastern and Asian countries, the disease affects more men than women. In the United States, it affects more women than men. Behcet's Disease tends to develop in people in their 20's or 30's, but people of all ages can develop this disease. Behcet's Disease is an autoimmune disease that results from damage to blood vessels throughout the body, particularly veins. In an autoimmune disease, the immune system attacks and harms the bodies' own tissues. The exact cause of Behcet's Disease is unknown. Most symptoms of the disease are caused by vasculitis (an inflammation of the blood vessels). Inflammation is a characteristic reaction of the body to injury or disease and is marked by four signs: swelling, redness, heat, and pain. Doctors think that an autoimmune reaction may cause the blood vessels to become inflamed, but they do not know what triggers this reaction. Under normal conditions, the immune system protects the body from diseases and infections by killing harmful "foreign" substances, such as germs, that enter the body. In an autoimmune reaction, the immune system mistakenly attacks and harms the body's own tissues. Behcet's Disease is not contagious; it is not spread from one person to another. Behcet's Disease affects each person differently. The four most common symptoms are mouth sores, genital sores, inflammation inside of the eye, and skin problems. Inflammation inside of the eye (uveitis, retinitis, and iritis) occurs in more that half of those with Behcet's Disease and may cause blurred vision, pain and redness. Other symptoms may include arthritis, blood clots, and inflammation in the central nervous system and digestive organs.*Behcet’s Disease has the ability to involve blood vessels of nearly all sizes and types, involving both veins and arteries. Because of the diversity and size of the* blood vessels affected, manifestations of Behcet’s may occur at many sites throughout the body. However, the disease seems to target certain organs and tissues, as described below: * Eye * Behcet’s may cause anterior uveitis (inflammation in the front of the eye) or posterior uveitis (inflammation in the back of the eye), and sometimes* both may be affected at the same time. * Anterior uveitis results in pain, blurry vision, light sensitivity, tearing or redness of the eye. * Posterior uveitis may be more dangerous and vision–threatening because it often causes fewer symptoms while damaging* the retina. * Mouth * Painful sores in the mouth called “aphthous ulcers” (known as oral aphthosis and aphthous stomatitis) affect almost all patients with Behcet's disease. Individual sores or ulcers are usually identical to canker sores, which are common in many people. These sores are usually a result of minor trauma. They are often the first symptom that a person notices and may occur long before any other symptoms appear. However, the lesions are more numerous, more frequent, and often larger and more painful. Aphthous ulcers can be found on the lips, tongue, and inside of the cheek. Aphthous ulcers may occur individually or in clusters, but occur in virtually all patients with Behcet’s. The sores usually have a red border and several may appear at the same time. They may be painful and can make eating difficult. Mouth sores go away in 10 to 14 days but often come back. Small sores usually heal without scarring, but larger sores may scar.* * * Skin * Skin problems are a common symptom of Behcet's disease. Skin sores often look red or resemble pus-filled bumps or a bruise. The sores are red and raised, and typically appear on the legs and on the upper torso. In some people, sores or*lesions may appear when the skin is scratched or pricked. When doctors suspect that a person has Behcet's disease, they may perform a pathergy test, in which they ***** the skin with a small needle; 1 to 2 days after the test, people with Behcet's disease may develop a red bump where the doctor pricked the skin. However, only half of the Behçet's patients in Middle Eastern countries and Japan have this reaction. It is less commonly observed in patients from the United States, but if this reaction occurs, then Behçet's disease is likely. * Pustular skin lesions that resemble acne, but can occur nearly anywhere on the body. This rash is sometimes called “folliculitis”. * Skin lesions called erythema nodosum: red, tender nodules that usually occur on the legs and ankles but also appear sometimes on the face, neck, or arms. Unlike erythema nodosum associated with other diseases (which heal without scars), the lesions of Behcet’s Disease frequently ulcerate. * Lungs * Aneurysms (outpouchings of blood vessel walls, caused by inflammation) of arteries in the lungs, rupture of which may lead to massive lung hemorrhage. * Joints * Arthritis or “arthralgias” which is inflammation of the joints, occurs in more than half of all patients with Behcet's Disease. Arthritis causes pain, swelling, and stiffness in the joints, especially in the knees, ankles, wrists, and elbows. Arthritis that results from Behcet's Disease usually lasts a few weeks and does not cause permanent damage to the joints. * Brain * Behcet's Disease affects the central nervous system in about 23 percent of all patients with the disease in the United States. The central nervous system includes the brain and spinal cord. Its function is to process information and coordinate thinking, behavior, sensation, and movement. Behcet's Disease can cause inflammation of the brain and the thin membrane that covers and protects the brain and spinal cord. This condition is called meningoencephalitis. People with meningoencephalitis may have fever, headache, stiff neck, and difficulty coordinating movement, and should report any of these symptoms to their doctor immediately. If this condition is left untreated, a stroke (blockage or rupture of blood vessels in the brain) can result. * Central nervous system involvement is one of the most dangerous manifestations of Behcet’s. The disease tends to involve the “white matter” portion of the brain and brainstem, and may lead to headaches, confusion, strokes, personality changes, and (rarely) dementia. Behcet’s may also involve the protective layers around the brain (the meninges), leading to meningitis. Because the meningitis of Behcet's Disease is not associated with any known infection, it is often referred to as “aseptic” meningitis. * Genitals * Genital sores affect more than half of all people with Behcet's Disease. The sores look similar to the mouth sores and may be painful. After several outbreaks, they may cause scarring. * Male — painful genital lesions that form on the scrotum, similar to oral lesions, but deeper. * Female — painful genital ulcers that develop on the vulva. * Gastrointestinal * Behcet's Disease causes inflammation and ulceration (sores) throughout the digestive tract that are identical to the aphthous lesions in the mouth and genital area. * Ulcerations may occur anywhere in the gastrointestinal tract from the mouth to the anus.* This leads to abdominal pain, diarrhea, and/or bleeding. Because these symptoms are very similar to symptoms of other diseases of the digestive tract, such as ulcerative colitis and Crohn's Disease, careful evaluation is essential to rule out these other diseases.* *
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