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

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

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 a rare disease that occurs almost
exclusively in smokers, generally young adults between 20 and 40 years old. Prognostic …

Pulmonary Langerhans cell histiocytosis (PLCH) is a well known entity in adults but is
exceedingly rare in children. It is better described in adults than in children. We describe the …

Adult pulmonary Langerhans cell histiocytosis (LCH) is a rare disorder of unknown aetiology
that occurs predominantly in young smokers with a peak incidence occurring between 20 to …

Objective To compare high-resolution (HR) CT and histopathological findings and to
evaluate serial CT findings in pulmonary Langerhans cell histiocytosis (PLCH). Methods We …

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 a rare interstitial lung disease of
unknown aetiology. We aimed to characterise a UK-wide cohort of patients with PLCH and …

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 …