Symptoms of Langerhans Cell Histiosis include an increased amount of neutrophils in the blood. The disease is often associated with diabetes insipidus, which causes frequent urination and kidney failure. Rare, fatal variants of this condition affect the liver, skin, and lungs, and are often accompanied by anemia and bleeding tendencies.
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If lesions infiltrate bones sufficiently, bone deformities can occur. Loss of teeth and bleeding gums are common, as are hearing loss and vision problems. Other symptoms of Langerhans Cell Histiosis include bumps, rash, and lesions on the skin. Although it is rare to pass the disease on to children, the disease can be inherited.
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Although the disease is uncommon, regular medical screening is crucial for detection and treatment. Some patients may be diagnosed with a skin-only form of Langerhans Cell Histiosis. However, this condition can progress to a multisystem form if left untreated. The condition can manifest itself in a number of ways, and it is vital to get diagnosed as soon as possible.
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Some of the most common symptoms of Langerhans Cell Histiosis are skin-only lesions. These lesions may affect the ear, cheeks, and roof of the mouth. Some patients develop a bluish rash that appears on the face. The resulting swelling may cause difficulty breathing. People with the disorder are also often prone to coughing or smoking.
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The underlying cause of Langerhans Cell Histiosis is unknown, but it can lead to lung cancer. The condition is not contagious, and there is no effective cure at this time. In addition to regular medical screening, people with the disorder should get regular medical checkups to determine the severity of the disorder. Depending on the severity of the disorder and its response to therapy, treatment may vary.
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Symptoms of Langerhans Cell Histiosis include sores in the cheeks, tongue, and roof of the mouth. In adults, the condition may cause bluish skin, tooth loss, and chest pain. It can also affect the hemiopoietic system, liver, and spleen. While the condition isn't inherited, it is difficult to detect in early stages.
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Symptoms of Langerhans Cell Histiosis can include chest pain and difficulty breathing. Those with Langerhans Cell Histiocysis may experience fatigue, bluish skin, and difficulty breathing. The disease can also cause a variety of other symptoms, such as fatigue, a bluish-blue color on the skin, and trouble breathing.
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Some symptoms of Langerhans Cell Histiosis include chest pain, difficulty breathing, and tiredness. During the early stages of the disease, the symptoms of Langerhans Cell Histyocytosis in infants may look like cradle cap or dandruff. The disease may also cause a bluish tint on the skin.
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Symptoms of Langerhans Cell Histiosis in infants include chest pain, difficulty breathing, and bluish skin. The disease is characterized by a bluish-purple rash on the skin. In adults with the disorder, there may also be an enlarged heart. A patient with this disease is at a higher risk of developing cardiovascular problems and kidney failure.
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The symptoms of Langerhans Cell Histiosis depend on the organs affected. In some cases, the disease may affect the liver and bone marrow. Affected individuals may also have delayed growth. The signs of Langerhans Cell Histiasis are different for different people. If you are experiencing any of these symptoms, seek medical attention immediately. You must be aware of these changes.
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There are no known long-term treatments for Langerhans Cell Histiosis. Most people with this condition have an irregular, yellowish tone to their skin. The disease is not painful. In severe cases, the skin may develop a white spot on the skin. Besides the lungs, other organs affected by Langerhans Cell Histiocytis are in the gastrointestinal tract, thyroid, and vulva.
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The condition is usually not life-threatening. In infants and children, it may go away without treatment. In older children and adults, treatment will depend on the location of the cells in the body and the risk of spreading the disease. The disease is typically asymptomatic, with symptoms that may be triggered by the onset of an infection. It is not known if any of these symptoms will lead to death, but the condition may require surgery in order to be completely eradicated.
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