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Revista médica de Chile

versión impresa ISSN 0034-9887

Resumen

OSSES A, RODRIGO; GONZALEZ B, SERGIO; AGUIRRE Z, MARCIA  y  SALDIAS P, FERNANDO. Adult pulmonary Langerhans cell histiocytosis: Report of one case. Rev. méd. Chile [online]. 2011, vol.139, n.2, pp.230-235. ISSN 0034-9887.  http://dx.doi.org/10.4067/S0034-98872011000200014.

Adult pulmonary Langerhans cell histiocytosis (PLCH) is a rare disorder of unknown etiology that occurs predominantly in young smokers, with an incidence peak at 20-40 years of age. In adults, pulmonary involvement with Langerhans cell histiocytosis usually occurs as a single-organ disease and is characterized by focal Langerhans cell granulomas infiltrating and destroying distal bronchioles. We report a 23-year-old asymptomatic male smoker with a non specific interstitial infiltrate found in preventive chest X ray examination. A high resolution chest CT scan showed multiple cystic structures predominating in the upper lobes, with small centrilobular nodules. A transbronchial biopsy showed a lymphocytic lung infiltrate with Langerhans cells. A surgical biopsy confirmed the diagnosis of pulmonary Langerhans cell histiocytosis. After six months of follow up, the patient is in good conditions.

Palabras clave : Dendritic cells; Histiocytosis, Langehaus-cell; Tobacco smoking.

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