Adult pulmonary Langerhans' cell histiocytosis is a rare disorder of unknown aetiology that
occurs predominantly in young smokers, with an incidence peak at 20–40 yrs of age. In …

Abstract Pulmonary Langerhans Cell Histiocytosis (PLCH) is a relatively uncommon lung
disease that generally, but not invariably, occurs in cigarette smokers. The pathologic …

Pulmonary Langerhans cell histiocytosis (PLCH) is an isolated form of Langerhans cell
histiocytosis that primarily affects cigarette smokers. PLCH is characterized by …

Pulmonary Langerhans' cell histiocytosis (PLCH) is an uncommon but important cause of
interstitial lung disease, and it occurs predominantly in adult cigarette smokers [1]. PLCH …

Abstract Background Pulmonary Langerhans cell histiocytosis (PLCH) is a rare interstitial
disease affecting primarily young adult smokers. In order to highlight the clinical features of …

Pulmonary Langerhans cell histiocytosis (PLCH) is an uncommon disorder of adult smokers
associated with a significant morbidity. Arising from the aberrant accumulation of …

Background Pulmonary Langerhans'-cell histiocytosis is an uncommon interstitial lung
disease in adults. It has an unpredictable course and may be associated with an increased …

Abstract Objectives Pulmonary Langerhans cell histiocytosis (PLCH) is a rare interstitial
granulomatous disease that usually affects young adults who are smokers. Chest computed …

We describe two patients with histologically proven pulmonary Langerhans' cell histiocytosis
in whom radiologic improvement occurred following smoking cessation. The patients had 23 …

Background The natural history of pulmonary Langerhans cell histiocytosis (PLCH) has
been unclear due to the absence of prospective studies. The rate of patients who experience …