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An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
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[Anatomoclinical study of annular elastolytic giant cell granuloma]
1Clinique dermatologique, université de Strasbourg, hôpitaux universitaires de Strasbourg, 1, place de l'Hôpital, 67091 Strasbourg cedex, France.
Annales De Dermatologie Et De Venereologie
|July 2, 2017
Summary
Annular elastolytic giant cell granuloma (AEGCG) and O'Brien actinic granuloma (AG) are histologically indistinguishable. The study suggests AEGCG should be considered synonymous with AG, with AEGCG being a more descriptive term.
Area of Science:
- Dermatopathology
- Histopathology
- Granulomatous skin diseases
Background:
- Annular elastolytic giant cell granuloma (AEGCG) and O'Brien actinic granuloma (AG) are rare, similar skin conditions.
- Previous literature lacks clear distinguishing features between AEGCG and AG.
Purpose of the Study:
- To identify distinguishing histopathological features between AEGCG and AG.
- To determine if AEGCG and AG are objectively different entities.
Main Methods:
- Single-center histopathology study of 73 cases classified as AEGCG or AG.
- Analysis using hematoxylin-eosin, orcein, and Alcian blue staining.
- Review of clinical data from request forms and patient files.
Main Results:
- No significant clinical or histological differences were found between AEGCG and AG cases.
- Both conditions showed granulomas with multinucleated giant cells and reduced/absent elastic tissue with elastophagocytosis.
- Lesions predominantly affected sun-exposed areas, presenting as annular erythematous plaques.
Conclusions:
- AEGCG should be assimilated with O'Brien actinic granuloma (AG).
- The term 'annular elastolytic giant cell granuloma' is more descriptive.
- Consider screening for sarcoidosis and diabetes in affected patients.
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