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Case Reports
. 2019 Dec 13;10(1):e2019133.
doi: 10.4322/acr.2019.133. eCollection 2020 Jan-Mar.

Pulmonary alveolar microlithiasis: Incidental finding - should we Ignore?

Affiliations
Case Reports

Pulmonary alveolar microlithiasis: Incidental finding - should we Ignore?

Manisha Agarwal et al. Autops Case Rep. .

Abstract

Pulmonary alveolar microlithiasis (PAM) is a rare entity, presenting mostly as an incidental finding. This disease has an autosomal recessive inheritance with inactivating mutations in the gene "solute carrier family 34 member 2". The present study was conducted to bring attention to this rare though preventable disease. The study was a cross-sectional descriptive study, conducted at the Department of Pathology, of a tertiary care hospital in New Dehli-India. PAMs were incidentally seen in two patients diagnosed with micronodular hepatic cirrhosis leading to reanalysis of 212 autopsies, retrospectively. Statistical analysis was done using Stata 14.0. We observed three forms (Type A, B and C) of round hyaline bodies measuring in diameter with thin delicate, radiating fibrils. These bodies were PAS positive, showed black discolouration of the pigment with von Kossa stain and birefringence on polarized microscopy using Congo red stain, however the refringence was light green as compared to apple green birefringence seen with amyloid deposition. PAM has a slow progressive course leading to a high rate of incidental detection. Drugs known to inhibit the micro-crystal growth of hydroxyapatite may slow the disease progression. The family members of patients with PAM may also be kept on follow up with regular imaging. Key messages: It is important to bring out the incidental finding as, seemingly innocuous observations may provide valuable insight into incurable diseases, especially rare diseases.

Keywords: Autopsy; Calcification, Physiologic; Incidental Findings.

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Conflict of interest statement

Conflict of interest: None

Figures

Figure 1
Figure 1. Photomicrographs of the lung showing in A - Pulmonary alveolar microlithiasis ‘Type A’; B - Pulmonary alveolar microlithiasis ‘Type B’ (A, B - H&E 400X); C - Pulmonary alveolar microlithiasis ‘Type C’ (H&E, 200X); D - Congo red stain (400X).
Figure 2
Figure 2. Photomicrographs of the lung showing in A – PAS stain, and B – von Kossa stain of type “B” microlith (400X). In B the inset shows in detail the microlith with granular pigment at the end of the fibrils.

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