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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Persistent pulmonary interstitial emphysema in a case of Langerhans cell histiocytosis
Pooja Abbey1, Mahender K Narula1, Rama Anand1
1Department of Radio-Diagnosis, Medical College and Associated Hospitals, New Delhi, India.
Abstract:
We present the case of a 10-month-old boy with multisystem Langerhans cell histiocytosis showing thin-walled lung cysts along with computed tomography (CT) evidence of persistent pulmonary interstitial emphysema (PPIE), in the absence of pneumothorax or pneumomediastinum. Follow-up CT performed after 6 months demonstrated complete resolution of interstitial emphysema.
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