Patients with Langerhans Cell Histiosis may experience some or all of the symptoms listed below. Treatment options vary depending on the extent of the disease and the affected organs. In some cases, the condition may be treated with observation and surgical removal of the affected area. Other treatment options include topical steroids, oral methotrexate, thalidomide, and radiation therapy.
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Symptoms of Langerhans Cell Histiosis include chest pain, difficulty breathing, and fatigue. Lesions may also develop on the skin. Although the condition is not inherited, the lesions can appear similar to other benign lesions found on the bones. If the lesions are large enough, they can cause problems such as bleeding gums and loose teeth. The lesions can also cause hearing loss.
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In infants, Langerhans cell histiocytosis symptoms include skin lesions, fingernails, and ulcers on the tongue, roof of mouth, and cheeks. In the most severe cases, the lesions may cause tooth loss. In older children, the disease may be accompanied by fever, earaches, and swollen neck and face.
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In children, symptoms of Langerhans Cell Histiocytes include fever, chest pain, and trouble breathing. It can also result in bluish skin and loose teeth. In smokers, the condition can lead to trouble breathing. The disease is usually diagnosed by a rash, but sometimes it can be confirmed with X-rays. A diagnosis cannot be made without a biopsy of the affected organs.
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A person with Langerhans Cell Histiocytes may have symptoms of fever, sores on the tongue, and loss of fingernails. In addition, the condition can lead to sores in the central nervous system and pituitary gland. Other symptoms include constant thirst, diabetes insipidus, and tooth loss. A doctor may perform X-rays or scans of the body's organs to confirm the diagnosis.
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People with Langerhans Cell Histiocytic disease may experience chest pain and difficulty breathing. In addition, they may experience bluish-red skin or a rash. A blood test may be necessary to confirm a diagnosis. Symptoms of Langerhans Cell Histiosis include bone lesions, hepatic dysfunction, and liver damage.
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The symptoms of Langerhans Cell Histiocytes include red, crusted papules on the skin. If these lesions spread in the bone, they can cause deformities, including a cradle cap or a dandruff-like rash. Occasionally, these lesions can result in ulcers. The disease is not inherited.
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The signs of Langerhans Cell Histiocytes include fatigue and chest pain. The skin may be blue-black. The disease can also be inherited and run in families. It is uncommon in children and is caused by an unknown cause. However, family history and exposure to certain chemicals may increase the risk. While the disease does not affect the organs directly, it can result in delayed growth.
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Symptoms of Langerhans Cell Histiocytes include skin rash, chest pain, and delayed growth. A child with this condition may have dandruff or a raised rash. X-rays and scans of internal organs may help confirm the diagnosis. A skin biopsy is not required, but may be useful for confirming the diagnosis.
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Besides the lung, the disease may also affect the liver and gastrointestinal tract. If these organs are affected, the condition can be life-threatening. Infections are common, and the lung can stiffen and become inflamed. The disorder is also associated with low platelets and a lack of hemoglobin. In some cases, symptoms can also occur in the lungs.
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The symptoms of Langerhans Cell Histiocytic disease are different in every patient. The disease can affect the lungs, liver, and the blood-forming system. If these organs are affected, the symptoms of Langerhans Cell Histocytosis can be life-threatening. This condition can be inherited or acquired. A doctor can diagnose the condition with a biopsy.
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Other symptoms of this condition include shortness of breath, coughing, and chest pain. The disease is usually asymptomatic and can progress to multifocal or disseminated form. It can also lead to serious complications such as lung collapse. If not diagnosed and treated, the symptoms of Langerhans Cell Histiocystis are often related to the presence of CSF1R.
