Patients with Langerhans cell histiocytosis will have symptoms that are specific to the organ or tissue they affect. Children are often diagnosed with the disease during childhood, but it can occur at any age. Smokers are most likely to experience the symptoms of the disease, as two-thirds of all adult cases affect the lungs. This condition will also cause a person to have shortness of breath and coughing. In rare cases, the disease may lead to lung collapse.
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The first symptom of Langerhans cell histiocytosis is fingernail loss. Eventually, it can lead to sores in the cheeks and roof of the mouth. If the lesion penetrates enough bone, it can cause problems such as bleeding gums and loose teeth. Some patients may experience hearing loss. Other symptoms of the disorder include skin lesions and bumps. Although these symptoms are not inherited, a family history of the disorder may increase the risk.
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Among the symptoms of Langerhans cell histiocytosis are chest pain and difficulty breathing. The disease is also known to cause tiredness, bluish skin, and trouble breathing. Some people with this disease also develop a fever and experience headaches. Those who smoke may also experience these symptoms, as they are more prone to develop lung problems and LCH.
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If you think your child may have Langerhans cell histiocytosis, it is important to see a pediatrician. If the condition affects a vital organ such as the heart, lungs, or thyroid, you should consult a doctor to get an accurate diagnosis. Treatment options are available for individuals with this condition, depending on the organ systems affected. A physician may recommend "watchful waiting" and regular monitoring.
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Some symptoms of Langerhans cell histiocytosis include sores on the tongue, roof of the mouth, and cheeks. Occasionally, the condition can lead to tooth loss. Some people may experience pain over a bone or in their face. Those with the disease may have to wear a mask to avoid being exposed to the cold. The condition can be difficult to detect, but it does not have any inherited symptoms.
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If the symptoms of Langerhans cell histiocytosis are mild or nonexistent, you may have the disease for years. If you have a diagnosis of Langerhans cell histiacytosis, you should see a doctor as soon as possible. However, it can be difficult to breathe when it's severe, and you may need to undergo a surgical procedure.
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Long-term effects of the disease can be permanent. The disease can cause bone deformities and result in a decreased quality of life. It can also cause severe bleeding and lead to a delayed growth. Symptoms of Langerhans cell histiocytosis can be accompanied by diabetes. If you experience any of these symptoms, seek medical attention immediately. It's important to seek professional advice as early as possible.
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The main symptoms of Langerhans cell histiocytosis include decreased white blood cells. Other than the symptoms mentioned above, these symptoms can also include fatigue, frequent infections, and low platelets. X-rays produce images of the bones, but the condition itself is not infectious. A blood test can help diagnose the condition. Your doctor will do various lab tests to confirm if you have the disease.
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Other symptoms of Langerhans cell histiocytosis include difficulty breathing, fingernail loss, and a bluish color to the skin. In adults, it can cause coughing and swelling of the face. It can also affect the nerves in the hands and feet. You should consult a doctor to learn more about these symptoms and to treat it. A medical professional can also help you determine the best treatment.
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Symptoms of Langerhans cell histiocytosis include a rash on the skin. It may be caused by a cancer or another disease. In addition to the rash, patients may also experience joint pain. Often, LCH is caused by an infection. The inflammation may not be a sign of Langerhans cell histiasis, but it is a symptom of the disease.
