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A Case of Langerhans Cell Histiocytosis with Atypical Radiological Presentation
Pulmonary Langerhans cell histiocytosis (PLCH) is a rare interstitial lung disease characterized by the accumulation of histiocytes within the airspaces or parenchyma of the lung. It almost always occurs in smokers between the ages of 20 and 40. Bronchoscopic interventions, such as transbronchial bi...
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| Pubblicato in: | Turk Thorac J |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Turkish Thoracic Society
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5793771/ https://ncbi.nlm.nih.gov/pubmed/29404095 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/ttd.2014.4110 |
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