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Recurrent bilateral spontaneous pneumothorax in early infancy: a case of langerhans cell histiocytosis
Iranian Journal of Radiology. 2005; 3 (1): 41-44
in English | IMEMR | ID: emr-71080
ABSTRACT
Langerhans cell histiocytosis [LCH] is a rare disorder characterized by infiltration of either single or multiple organs by S100 and CD1a positive cells. Patients with pulmonary LCH are predisposed to pneumothorax due to destructive changes in the lung parenchyma. Here, we report a case of multisystem LCH who presented at 2 months of age with simultaneous bilateral spontaneous pneumothorax
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Index: IMEMR (Eastern Mediterranean) Main subject: Pneumothorax / Microscopy, Electron / Radiography, Thoracic / S100 Proteins / Tomography, X-Ray Computed / Eosinophilic Granuloma / Histiocytosis, Langerhans-Cell Type of study: Case report Limits: Female / Humans Language: English Journal: Iran. J. Radiol. Year: 2005

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Index: IMEMR (Eastern Mediterranean) Main subject: Pneumothorax / Microscopy, Electron / Radiography, Thoracic / S100 Proteins / Tomography, X-Ray Computed / Eosinophilic Granuloma / Histiocytosis, Langerhans-Cell Type of study: Case report Limits: Female / Humans Language: English Journal: Iran. J. Radiol. Year: 2005