Foreign Body Granulomatous Reaction Presenting as Systemic Sarcoidosis: A Case Report with Energy-Dispersive Spectroscopy Analysis
Michael Singer,* Herb Srolovitz,
Robin Bullick, and André Dufresne
Background: Sarcoidosis is an immune-mediated idiopathic disorder and is generally thought to be a diagnosis of exclusion. Although researchers have looked at viruses, mycobacteria, and certain chemicals as possible triggers, the initiating antigen remains unidentified.
Observations: A 41-year-old black male metal-worker previously diagnosed with systemic sarcoidosis presented with a 6-month history or recurrent, sometimes tender, skin nodules on the lower legs. Chest film, gallium scan, and angiotensin-converting enzyme (ACE) level results supported a diagnosis of systemic sarcoidosis. A biopsy of a lower extremity skin nodule showed confluent non-necrotizing granulomas with irregular birefringent particles in giant cells in a fibrous tissue background suggestive of a silica nodule. Review of a previous bronchila biopsy showed similar foreign body granulomas. Energy-dispersive spectroscopy (EDS) analysis, clay (kaolinite), chromium, and aluminum particles that were consistent with the patient's occupational exposure.
Conclusion: ACE level and gallium scan may not be specific for sarcoidosis. In certain occupational settings, EDS analysis should be considered before a diagnosis of sarcoidosis is made. This case may provide insight into the etiology of certain presentations labelled as sarcoidosis.
Full text available in the print edition / Pour le texte intégral veuillez consulter la version imprimée.
JCMS 1(1) Contents