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Langerhans Cell Histiocytosis Symptoms - Oren Zarif - Langerhans Cell Histiocytosis


Children and infants with Langerhans Cell Histiocystsis symptoms may go away on their own without treatment. Depending on the location of the affected cells and the organs involved, a child may need to undergo various treatments to prevent the disease from progressing to a more serious state. Although the disease has a high mortality rate, children with localized and mild cases of the condition often have a prolonged life expectancy.

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Symptoms of Langerhans Cell Histiocysts may be sporadic or systemic. In the early stages, the disease is not life-threatening. If left untreated, it may lead to chronic infections. As it progresses, the symptoms of this disease may become more serious and lead to the development of complications, such as delayed growth.

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Patients with a diagnosis of Langerhans Cell Histiocysts may experience chest pain, trouble breathing, and fatigue. Some people may also have bluish skin. Smokers may have bluish patches on their skin. However, if a patient has any of these symptoms, it is best to seek medical attention right away. If you have any of the symptoms above, see your doctor immediately.

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If the condition isn't treated within a month, it can progress to a more severe form. If the problem affects the heart, liver, or lungs, medical treatment will help to control the condition. In more severe cases, surgical treatment may be required. Surgical removal of the affected lesion is usually straightforward, but the spine may need to be reinforced. In addition to surgery, the patient may be prescribed low-dose chemotherapy to control the disease.

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The most common symptoms of Langerhans Cell Histiocysts are difficulty breathing, chest pain, and tiredness. As the disease develops, the affected person may have difficulty breathing and may have difficulty urinating. Adults with this condition may experience bluish patches on their skin and difficulty breathing. While the disease is not genetic, the symptoms are often very common in patients with the disorder.

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In infants with Langerhans Cell Histiocystsis, the condition may affect the skin only. If the condition is confined to the skin, the symptoms can worsen over time. The affected child may also experience dandruff or cradle cap. In infants, the condition may cause a raised rash on the face and hair.

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Other symptoms of Langerhans Cell Histiocysts are chest pain, tiredness, and bluish color of the skin. In adults, Langerhans Cell Histiosis symptoms include trouble breathing, chest pain, and tiredness. Some patients also experience bluish patches on their skin. In children, it is common to have an infection in the affected area.

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Symptoms of Langerhans Cell Histiocystsis include chest pain, difficulty breathing, and bluish-green skin. The condition can be severe and require treatment. It may also result in delayed growth. In children, Langerhans cell histiocystsis symptoms are often similar to those of other conditions, including asthma.

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In infants, Langerhans Cell Histiocystsis symptoms may begin on the skin, but can progress to multiple systems over months. It may be initially difficult to diagnose, but it can be easily treated with a combination of medications and medical supervision. Some people with this condition do not experience any symptoms. Other symptoms of Langerhans Cell Histiosis are characterized by anemia, enlarged liver, anemia, and bleeding tendencies.

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The symptoms of Langerhans Cell Histiocysis include pain, swelling, and numbness. Other symptoms include fever, anemia, and arthritic pain. In the most severe cases, a patient may experience a lump on the skin or on the stomach. There are no specific treatments for Langerhans Cell Histiosis, though there are some symptomatic measures a patient can take to deal with it.

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Depending on the location of the tumor, Langerhans Cell Histiocysts may cause pulmonary damage. The disease may lead to tumors and inflammation in the central nervous system. Additionally, the symptoms of Langerhans Cell Histiosis can include constant thirst, diabetes insipidus, and lung stiffness. The diagnosis of Langerhans Cell Histiactics should be determined by an examination of the affected areas of the body, including the spinal cord and brain.

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