This review addresses the pathology of lung disease in which the predominant finding is
diffuse cystic change. Although cysts may be found radiologically in a wide variety of …

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 …

Background The pediatric pulmonary multisystem Langerhans cell histiocytosis (PPM LCH)
is associated with either low risk or high risk organ (s). The nodulo-cystic lung lesions …

Background Pulmonary Langerhans cell histiocytosis (PLCH) determines reduced exercise
capacity. The speculated mechanisms of exercise impairment in PLCH are ventilatory and …

Background An important objective on diagnosis of patients with Langerhans cell
histiocytosis (LCH) is to determine the extent of disease. However, whether systematic …

Histiocytes of Langerhans cell type are recovered from the bronchoalveolar lavage fluid
(BALF) of patients with interstitial lung diseases in a nonspecific manner. Langerhans cells …

BACKGROUND Langerhans cell histiocytosis (LCH) is a rare disease of unknown aetiology.
While it may affect any organ of the body, few cases of solitary lung involvement are …

A lung cyst is an air-filled lucent structure surrounded by a thin wall. The presence of
multiple intrapulmonary cysts is defined as cystic lung disease. Although cystic lung disease …

Langerhans cell histiocytosis (LCH) is a rare myeloid neoplasm characterized by the
proliferation and dissemination of histiocytes. These in turn may cause symptoms ranging …

Abstract Pulmonary Langerhans Cell Histiocytosis (PLCH) is a diffuse lung disease that
primarily affects young adults, with cigarette smoking playing a significant role in developing …