Cystic fibrosis (pulmonary manifestations)
1 week history of worsening wet cough.
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Right-sided Port-A-Cath is appropriately projected with the tip at the superior atriocaval junction. Coarse interstitial markings and dilated bronchi. No collapse or consolidation. The pleural reflections are clear. The cardiomediastinal outline is normal.
These findings are typical of cystic fibrosis.