Pulmonary alveolar microlithiasis

Case contributed by Dalia Ibrahim
Diagnosis almost certain

Presentation

Severe dyspnea. Her physician suspected interstitial lung disease.

Patient Data

Age: 50 years
Gender: Female

Innumerable sand-like calcifications throughout the lungs, predominantly in mid & lower zones, sparing the apices, with subpleural and peribronchial distribution, crazy paving pattern, calcified interlobular septa and black pleura sign.

Fibrotic changes in the right apex with several small bullae.

Dilated pulmonary trunk and main pulmonary arteries.

Cardiomegaly, mild pericardial effusion.

Upper abdominal slices - hepatomegaly and mild ascites.

Case Discussion

Pulmonary alveolar microlithiasis (PAM) is a rare idiopathic condition characterized by widespread intra-alveolar deposition of spherical calcium phosphate microliths.

How to use cases

You can use Radiopaedia cases in a variety of ways to help you learn and teach.

Creating your own cases is easy.

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.