Fibrocartilaginous metaplasia identified in the long head of the biceps brachii

• Published in: Journal of shoulder and elbow surgery Vol. 27; no. 7; pp. 1221 - 1225
• Main Authors: Bottegoni, Carlo, Farinelli, Luca, Aquili, Alberto, Manzotti, Sandra, Baldini, Marco, Gigante, Antonio
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-07-2018
• Subjects: Cartilage metaplasia; compression loading; long head of the biceps brachii; short head of the biceps brachii; tendon degeneration; tendon rupture; tendon degeneration; short head of the biceps brachii; Basic Science Study; tendon rupture; Histology; Cartilage metaplasia; long head of the biceps brachii; compression loading
• ISSN: 1058-2746; 1532-6500
• DOI: 10.1016/j.jse.2018.02.042

In the glenohumeral joint, the long head of biceps brachii (LHBB) is exposed to tension and compression loading. The short head of biceps brachii (SHBB) works only in tension. It is known that tendon under compression might develop fibrocartilaginous metaplasia that improves the resistance to compression but reduces the resistance to tension. This study evaluated the presence of cartilage in LHBB and SHBB samples, supporting its possible role in tendon tear.
Between 2014 and 2016, 13 samples of LHBB and SHBB were collected during surgery for shoulder instability, glenohumeral arthritis, and massive rotator cuff tears. The samples were stained with hematoxylin and eosin, safranin-O, and Alcian blue (pH 1.0) for light microscopy. Immunohistochemistry was performed using anti-S100, anti-collagen I and II, and anti–tenascin-C antibodies.
Histochemistry: LHBB samples showed matrix disorganization, with clusters of chondrocyte surrounded by collagen fibers and glycosaminoglycans. Safranin-O showed evident metachromasia. SHBB samples did not show any matrix disorganization or cartilaginous metaplasia. Immunohistochemistry: In all LHBB samples, anti-S100 and anti-collagen II showed cartilage in proximity of the tendon tear. Tenascin C immunostained closely to the disorganized matrix areas. SHBB, however, showed no positive areas for S-100, anti-collagen II, or tenascin C.
According to our results, we hypothesize that the repeated stimulation in compression may induce the formation of fibrous cartilage. However, to date its role in tendon pathology remains to be clearly defined.