Synovial samples were preferentially obtained from the most grossly inflamed (dull and opaque) area of the synovium. If there was no obviously inflamed synovium, samples were obtained from standard locations: the femoral aspects of the medial and lateral gutters and the central supratrochlear region of the suprapatellar pouch. OA synovial tissue samples were formalin-fixed and paraffin-embedded, and the RA tissues were fresh-frozen in optimal cutting temperature compound. Each tissue biopsy was sectioned at 5-μm thickness and stained with Harris-modified hematoxylin solution and eosin Y (H&E) manufactured by Epredia in Kalamazoo, MI. An expert musculoskeletal pathologist (ED) scored fourteen synovial histologic features in a single section for each patient: lymphocytic inflammation, mucoid change, fibrosis, fibrin, germinal centers, lining hyperplasia, neutrophils, detritus, plasma cells, binucleated plasma cells, Russell bodies, sub-lining giant cells, synovial lining giant cells, and mast cells. Detailed methods for scoring these features are included in the
Histopathological Evaluation of Synovial Tissue in OA and RA
Synovial samples were preferentially obtained from the most grossly inflamed (dull and opaque) area of the synovium. If there was no obviously inflamed synovium, samples were obtained from standard locations: the femoral aspects of the medial and lateral gutters and the central supratrochlear region of the suprapatellar pouch. OA synovial tissue samples were formalin-fixed and paraffin-embedded, and the RA tissues were fresh-frozen in optimal cutting temperature compound. Each tissue biopsy was sectioned at 5-μm thickness and stained with Harris-modified hematoxylin solution and eosin Y (H&E) manufactured by Epredia in Kalamazoo, MI. An expert musculoskeletal pathologist (ED) scored fourteen synovial histologic features in a single section for each patient: lymphocytic inflammation, mucoid change, fibrosis, fibrin, germinal centers, lining hyperplasia, neutrophils, detritus, plasma cells, binucleated plasma cells, Russell bodies, sub-lining giant cells, synovial lining giant cells, and mast cells. Detailed methods for scoring these features are included in the
Corresponding Organization : Hospital for Special Surgery
Other organizations : Columbia University, Cornell University, Stanford University, Mitre (United States), Rockefeller University
Variable analysis
- Synovial sample source (OA vs. RA patients)
- Synovial histologic features (lymphocytic inflammation, mucoid change, fibrosis, fibrin, germinal centers, lining hyperplasia, neutrophils, detritus, plasma cells, binucleated plasma cells, Russell bodies, sub-lining giant cells, synovial lining giant cells, and mast cells)
- Preference for obtaining samples from grossly inflamed synovial areas
- Preference for obtaining samples from standard locations (femoral aspects of the medial and lateral gutters and the central supratrochlear region of the suprapatellar pouch) if no obviously inflamed synovium was present
- Formalin-fixation and paraffin-embedding for OA samples
- Fresh-freezing in optimal cutting temperature compound for RA samples
- Sectioning of tissue samples at 5-μm thickness
- Staining with Harris-modified hematoxylin solution and eosin Y (H&E)
- Not specified
- Not specified
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