Initial tissue preparation and fixation.
Treatment with periodic acid to oxidize carbohydrates in fungal cell walls to aldehydes.
Application of methenamine silver solution, which deposits silver in the presence of aldehydes.
Toning with gold chloride to enhance contrast.
Counterstaining with light green or other suitable stains to provide background contrast.
High sensitivity for detecting
pathogens with polysaccharide-rich cell walls.
Distinct black staining of
fungal elements against a green or other contrasting background.
Ability to identify
fungal structures in tissue sections that might be missed with other staining methods.
It can be time-consuming and requires multiple steps.
Non-specific staining may occur, leading to potential false positives.
Interpretation of results may require a skilled histologist or pathologist.
Conclusion
The Gomori Methenamine Silver stain remains a cornerstone in histopathology for its ability to reliably detect fungal and certain bacterial elements within tissue samples. Its utility in clinical diagnostics underscores its importance, despite some inherent limitations. Proper application and interpretation of the GMS stain can provide critical insights into various infectious and pathological conditions.