Title of article :
Pulmonary Langerhans Cell Histiocytosis and Diabetes Insipidus in a Young Smoker
Author/Authors :
Earlam, K. Division of Respirology - The Ottawa Hospital - University of Ottawa, Ottawa, Canada , Souza, C. A. Department of Medical Imaging - The Ottawa Hospital - University of Ottawa, Ottawa, Canada , Glikstein, R. Department of Medical Imaging - The Ottawa Hospital - University of Ottawa, Ottawa, Canada , Gomes, M. M. Department of Pathology and Laboratory Medicine - The Ottawa Hospital - University of Ottawa, Ottawa, Canada , Pakhale, S. Division of Respirology - The Ottawa Hospital - University of Ottawa, Ottawa, Canada
Pages :
6
From page :
1
To page :
6
Abstract :
Langerhans cell histiocytosis is characterized by the abnormal nodular proliferation of histiocytes in various organ systems. Pulmonary involvement seen in young adults is nearly always seen in the context of past or current cigarette smoking. Although it tends to be a single-system disease, extrapulmonary manifestations involving the skin, bone, and hypothalamic-pituitary-axis are possible. High resolution CT (HRCT) of the thorax findings includes centrilobular nodules and cysts that are bizarre in shape, variable in size, and thin-walled. Often the diagnosis can be made based on the appropriate clinical presentation and typical imaging findings. Treatment includes smoking cessation and the potential use of glucocorticoids or cytotoxic agents depending on the severity of disease and multisystem involvement.
Keywords :
Pulmonary Langerhans , Cell Histiocytosis , Diabetes Insipidus
Journal title :
Canadian Respiratory Journal
Serial Year :
2016
Full Text URL :
Record number :
2607276
Link To Document :
بازگشت