Abstract:Pulmonary Langerhans cell histiocytosis (PLCH) is a rare interstitial lung disease. Young male adults develop the disease most frequently. Greater than 90% of cases of PLCH occur in smokers. Diabetes insipidus (DI) occurs in about 11% to 40% of patients and pneumothoraces occur in 10% to 30% of patients. The diagnosis of PLCH can be confirmed by BAL, transbronchial biopsy, or surgical lung biopsy.
CASE REPORTA 19-year-old male presented with a four-week history of dyspnea and hemoptysis which had begun after t… Show more
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