A number of tests may be conducted to diagnose Langerhans cell histiocytosis. These include urine and blood tests, as well as bone marrow and bone scans. A biopsy of the lesion's cells is often necessary to confirm its diagnosis. In rare cases, patients may also have other problems. Some patients may develop chronic lung dysfunction. A physician may perform a needle biopsy to diagnose Langerhans cell histitis.
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Besides blood cell count, Langerhans cell histiocytosis also affects the lungs and liver, three important organs in the body's blood-forming system. Because of the seriousness of this disease, doctors may recommend treatment of the condition. In many cases, the disease does not require surgery, and most children will recover without any long-term complications.
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Symptoms of Langerhans cell histiocytosis include bluish skin color, fingernail loss, and sores on the roof of the mouth, tongue, and cheeks. Additionally, individuals with this disorder may experience pain over the bones and a swelling of the face. If these symptoms occur, the patient should seek medical care immediately. The disease can lead to a variety of complications, including anemia and heart failure.
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Other symptoms of Langerhans cell histiocytosis include fingernail loss and sores on the tongue, inside cheeks, and roof of the mouth. A few people with this disease may also experience bleeding gums or ulcers. Although there is no known inherited cause, symptoms of Langerhans cell histitiocytosis can lead to tooth loss and difficulty breathing.
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Other symptoms of Langerhans cell histiocytosis include fingernail loss, sores on the roof of the mouth, and inside the cheeks. Occasionally, a patient may have a bluish skin rash or face lesions. There are no known inherited symptoms of Langerhans cell histitiocytosis.
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The symptoms of Langerhans cell histiocytosis include skin-only lesions and a loss of fingernails. In some cases, the disease may progress to multisystem Langerhans cell histiosis, or cradle cap. The condition can worsen over months and can cause a raised skin rash. Eventually, the disease may lead to a bluish rash, or even ulcers.
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If the lesions infiltrate the bone, they may cause bone deformities. The lesions can affect the jaw and may result in loose teeth, bleeding gums, or a bluish skin rash. Other signs of Langerhans cell histiocytosis include difficulty breathing, a bluish skin rash, and an itchy or inflamed tongue.
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Symptoms of Langerhans cell histiocytosis may include chest pain, fatigue, and a bluish-white rash. If the lesions infiltrate the bones deeply enough, they can cause bone deformities. If not treated, patients may experience hearing loss or difficulty breathing. X-rays and scans of the ear bones may help diagnose the disease.
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Other symptoms of Langerhans cell histiocytosis include loss of fingernails and mouth ulcers. A patient may experience sores on the tongue, cradle cap, and roof of the mouth. The condition may cause difficulty breathing and even ulcers. In addition to the skin, a person may experience other symptoms such as fever, headache, and stomach aches.
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Although the exact cause of Langerhans cell histiocytosis is not known, genetics and exposure to certain chemicals may increase a person's risk. The symptoms of Langerhans cell histicytosis may include: (a) atypical spleen, enlarged liver, and atypical lymphocytes.
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Langerhans cell histiocytosis is caused by the proliferation of dendritic mononuclear cells in the lungs and other organs. The condition may also affect the hemiopoietic system and the spleen. For these reasons, the best way to diagnose and treat Langerhans cell histiosis is with a proper diagnosis and treatment.
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In addition to the symptoms of lung and liver damage, Langerhans cell histiocytosis can also affect the liver and blood-forming system. These organs are at risk of damage and in some cases, it can be life-threatening. Lung involvement can cause swollen and stiffened airways and breathing difficulties. Hematopenia and pancytopenia are other symptoms of LCH.