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Popper, HH.
[Pulmonary Langerhans cell histiocytosis].
Pathologe. 2015; 36(5):451-457 Doi: 10.1007/s00292-015-0052-9
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Führende Autor*innen der Med Uni Graz
Popper Helmuth
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Abstract:
Pulmonary Langerhans cell histiocytosis is regarded as a reactive proliferation of the dendritic Langerhans cell population stimulated by chronic tobacco-derived plant proteins due to incomplete combustion but can also occur in childhood as a tumor-like systemic disease. Currently, both these forms cannot be morphologically distinguished. In the lungs a nodular proliferation of Langerhans cells occurs in the bronchial mucosa and also peripherally in the alveolar septa with an accompanying infiltration by eosinophilic granulocytes and destruction of the bronchial wall. Langerhans cells can be selectively detected with antibodies against CD1a and langerin. In the reactive isolated pulmonary form, abstinence from tobacco smoking in most patients leads to regression of infiltration and improvement of symptoms. In high-resolution computed tomography (HRCT) the small star-like scars can still be detected even after complete cessation of tobacco smoking.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Antigens, CD - analysis
Antigens, CD1 - analysis
Cell Proliferation - physiology
Child -
Dendritic Cells - pathology
Histiocytosis, Langerhans-Cell - pathology
Histiocytosis, Langerhans-Cell - therapy
Humans -
Langerhans Cells - pathology
Lectins, C-Type - analysis
Lung - pathology
Lung Diseases, Interstitial - pathology
Lung Diseases, Interstitial - therapy
Mannose-Binding Lectins - analysis
Microscopy, Electron -
Smoking - adverse effects
Smoking Cessation -
Tomography, X-Ray Computed -

Find related publications in this database (Keywords)
Langerhans cells
Nodular proliferation
Tobacco smoking
CD1a
Langerin
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