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Symptoms of Langerhans Cell Histiocytosis - Oren Zarif - Langerhans Cell Histiocytosis


Symptoms of Langerhans Cell Histiosis may include multiple small bumps and crusted patches of skin. While the condition is not cancerous, the disease can lead to serious complications. Children with the disorder may have a prognosis of forty to fifty percent. This type of histiocytosis is uncommon in adults, although it is common in young children.

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There are several symptoms of Langerhans cell histiocytosis. People with the disorder may have fingernail loss, sores on the tongue, inside cheeks, and on the roof of the mouth. It can also cause bone deformities. Lesions in the ear bones can lead to hearing loss. The condition can also present with lesions on the skin. Typically, this disease is not hereditary, but it can occur in families with a history of the disease.

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Symptoms of Langerhans cell histiocytosis include fingernail loss, sores on the roof of the mouth, sores inside the cheeks, and tooth loss. In rare cases, the condition may lead to pain over the bones, a bluish skin color, and bleeding tendencies. If you are experiencing these symptoms, consult your doctor immediately.

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If you are suffering from Langerhans cell histiocytosis, you should seek medical care immediately. It is often difficult to treat, but your doctors will do everything they can to help you. Treatments for Langerhans cell histiosis may include surgery or bisphosphonate therapy. If you are concerned about the symptoms of this disease, contact your doctor immediately.

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Symptoms of Langerhans cell histiocytosis include loss of fingernails, sores on the tongue, and sores on the roof of the mouth. Some patients may experience difficulty breathing, swelling of the face, or pain in the bones. These symptoms may be indicative of LCH. If you have these symptoms, you should visit your doctor as soon as possible.

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Some symptoms of Langerhans cell histiocytosis include loss of fingernails, sores on the cheeks and roof of the mouth, and cradle cap. If you suspect that you have Langerhans cell histiosis, you should consult your doctor immediately. It is important to follow the condition carefully, as it can lead to cancer or spread of the disease.

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Other symptoms of Langerhans cell histiocytosis include bluish skin, fingernail loss, and sores on the tongue, cheeks, and roof of the mouth. In smokers, these symptoms may include chest pain, trouble breathing, and swelling of the face and neck. In severe cases, blood pressure may become elevated and difficulty breathing.

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Early symptoms of Langerhans cell histiocytosis may include chest pain, bluish skin, fatigue, and trouble breathing. In infants, the disease may be asymptomatic, and it may only be a symptom of another illness. As it develops, it may lead to a variety of other problems, including heart failure and stroke.

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The symptoms of Langerhans Cell Histiosis can range from minor chest pain to a more serious disease. If a rash is present, it can be a sign of the disease, but it is unlikely to be a cause of concern. If the lesions spread to bones, however, it may lead to bone deformities and ulcers. While this condition is not inherited, it may occur in smokers.

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While Langerhans Cell Histiosis is not a disease of the skin, it can affect the pituitary gland. This gland produces hormones that control various body functions, including growth. It is important to note that Langerhans Cell Histiozyocytosis is not a skin disease. It is a condition of the pituitary gland that affects the bones.

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Symptoms of Langerhans Cell Histiosis vary depending on the organs involved. Often, PLCH is accompanied by shortness of breath, chest pain, and coughing. If the disease is not diagnosed and treated in time, it can lead to lung collapse and other serious complications. To find out if it's a lung disorder, contact your doctor.

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Although LCH is rare, it can occur in adults and children of all ages. Most cases occur in children between ages one and 15 years, though the condition can occur in people of any age. Its onset is usually accompanied by a rash similar to cradle cap. Symptoms of Langerhans Cell Histiocysis can be difficult to identify, so it is important to seek medical help if necessary.

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