Journal of Cardio-Thoracic Medicine (Sep 2022)

Pulmonary Alveolar Microlithiasis Diagnosed During Video-Assisted Thoracoscopic Surgery; A Case Report

  • Amir Mohammad Hashem Asnaashari,
  • Davood Attaran,
  • Soroush Attaran,
  • Parastou Asnaashari,
  • Sahar Ravanshad,
  • Sepide Hejazi

DOI
https://doi.org/10.22038/jctm.2022.66087.1383
Journal volume & issue
Vol. 10, no. 3
pp. 1039 – 1043

Abstract

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Pulmonary alveolar microlithiasis (PAM) is a rare inherited pulmonary disease characterized by the deposition of intra-alveolar calcium deposits. In most of the Asian and European countries, PAM is usually misdiagnosed as pulmonary tuberculosis and sarcoidosis. We presented a young case of PAM manifested as chronic progressive dyspnea unresponsive to corticosteroids for one year. The first diagnostic clues were made by high resolution computed tomography. Although Bronchoalveolar lavage and transbronchial lung biopsy examination were unremarkable, however, after performing a Video-assisted thoracoscopic surgery, the biopsy specimens confirmed the diagnosis of PAM.

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