Langerhans Cell Histiocytosis Symptoms - Oren Zarif - Langerhans Cell Histiocytosis

Among the many symptoms of Langerhans cell histiocytosis is the loss of fingernails, sores on the roof of the mouth, inside the cheeks, and on the tongue. People suffering from this disease may also experience difficulty breathing and bone pain. The disease is usually asymptomatic, but can cause severe complications. It may also cause bleeding tendencies and pain over bones.

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The symptoms of Langerhans cell histiocytosis range from a mild case to a multi-organ disease that causes severe fatigue and a rash. It can develop into a progressive and disseminated form if the condition is not diagnosed early. The disease can also progress to multi-organ failure. However, despite the lack of symptoms, patients with Langerhans cell histiosis should be evaluated by a healthcare professional.

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Although the exact causes of Langerhans cell histiocytosis are unknown, genetic and environmental factors may increase the risk. Certain chemicals can increase the chances of developing this disorder. It may also cause delayed growth in children. To determine whether you are at risk, contact your doctor and get tested. You may need to undergo a blood test. While there is no cure for this disorder, you can take some steps to reduce your chances of death.

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If you suspect that you have Langerhans cell histiocytosis, consult your physician immediately. If you have a child who has symptoms of the disease, your doctor can run a few tests to rule out other diseases. The patient must be closely monitored for any additional symptoms, including pulmonary infiltrates or bone lesions. In addition to blood tests, your doctor will likely order a CT scan to confirm the diagnosis.

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If you have bone lesions, your doctor will perform an x-ray. If the lesions affect multiple bones, they may cause hearing loss, loose teeth, or bleeding gums. Your doctor will also examine you for skin lesions. Because Langerhans cell histiocytosis is not inherited, treatment options vary according to the organs and tissues involved. Symptoms of the disease depend on the organs and tissues affected.

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If your child has lung, bone, or marrow lesions, your doctor will recommend appropriate treatment. Treatment options may vary depending on the organs affected. Observation and surgical removal of the lesion may be sufficient. Topical steroids, oral methotrexate, and thalidomide are common treatments for isolated skin lesions. If your child has systemic symptoms, chemotherapy may be necessary.

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When Langerhans cell histiocytosis is suspected in a child, the symptoms include pulmonary infiltrates, bone lesions, and bone pain. In addition, there are several different types of symptoms. The most common are: cutaneous manifestations (rashs), and ocular lesions. If you have these symptoms, it may be Langerhans Cell Histiocysis.

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If you're worried about symptoms, see your pediatrician. Hematologists and radiologists at the Dana-Farber/Boston Children's Histiocytosis Program have extensive experience treating patients with this rare disease. They are also involved in clinical research related to Langerhans cell histiocytosis. If your child is experiencing any of these symptoms, you should seek medical attention.

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The symptoms of Langerhans cell histiocytosis are similar to those of other diseases. A patient suffering from this disease may suffer from pulmonary infiltrates, bone lesions, and other signs and symptoms of a lung disease. If your child has any of these symptoms, he or she may be suffering from Langerhans cell histiosis.

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The symptoms of Langerhans cell histiocytosis are similar to those of other diseases. These cells are abnormally proliferating and infiltrating various organs in the body, including the brain, spinal cord, and the nervous system. These cells may cause tumors and other problems in the body. If you're affected by this condition, you should seek medical attention immediately.

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Langerhans cell histiocytosis is a rare cancer. This cancer is characterized by the overproduction of hematopoietic cells, which include T-cells. They are normally found in the epidermis. This type of disease starts in the skin and affects children between five and ten years old. As a result, the disease is inherited and does not spread.