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Eosinophilic granuloma - X-ray of the skull Respiratory system
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Histiocytosis
Alternative Names: Eosinophilic granuloma; Pulmonary histiocytosis X; Nonlipid reticuloendotheliosis; Pulmonary langerhans cell granulomatosis; Hand-Schuller-Christian disease; Letterer-Siwe disease; Langerhans cell histiocytosis Treatment: This disorder is treated with corticosteroids, which suppress immune function (including the dangerous cells). Smoking may worsen the response to treatment and should be stopped. Text Continues Below Children may be given other medications depending on their estimated prognosis, including: Methotrexate Vinblastine Cyclophosphamide Etoposide Radiation therapy or limited surgery may also be used to treat bone lesions. Patients are also treated with supportive care to reduce symptoms and treat infections that may occur when the immune system is compromised. Treatment may include antibiotics, breathing assistance with a respirator, physical therapy, selenium-based shampoo for scalp problems, and hormone replacement to deal with hormonal dysfunction. Support Groups: For additional information, patients may wish to contact the Histiocytosis Association of America at 800-548-2758. Expectations (prognosis): In pulmonary histiocytosis, the disease stabilizes or improves in about one-half of the affected people and the other half progress to a permanent loss of lung function. In the pediatric versions, it depends on the actual disease category and severity of the disease. Some can be expected to have a normal life span with minimal disease involvement and some can expect a poor outcome. Complications: Spontaneous pneumothorax Diffuse interstitial pulmonary fibrosis Page:  1 | 2 | Next >>