Abstract
Objective: Finger flexion contractures are an important cause of disability in patients with systemic sclerosis (SSc); however, their pathophysiology is poorly understood Our aim was to assess feasibility of scanning finger flexor tendons in patients with SSc and explore the ultrasound findings in these tendons, including measurement of finger flexor tendon complex (FFTC).
Methods: Grey Scale and Power Doppler ultrasound assessment of the FFTC including tendon structure and surrounding soft tissue. Measurements of the FFTC (A1 pulley, tendon and palmar plate) were made. Feasibility was assessed by the number of fingers which could be measured.
Results: We studied the second to fifth flexor tendons (n=160) of both hands in 20 patients with SSc, including early and established disease. We were able to assess the FFTC and make measurements of the flexor tendon and palmar plate in all (n=40) and A1 pulley in almost all (n=39) of the studied fingers. Common pathologies identified included peritendinous (n=12) and soft tissue (n=8) calcification. Tendon thickening was seen in 6 patients, but synovitis/tenosynovitis was rare. The A1 pulley was thickened in patients with SSc (0.46mm), in particular, those with diffuse cutaneous SSc (0.50mm).
Conclusion: We were able to successfully assess, including making measurements of, the FFTC in patients with SSc. Our study showed calcifications in the peritendinous areas and soft tissue and thickening of the A1 pulley. These findings may play a role in the pathophysiology of SSc-hand contractures by causing mechanical impingement of the finger flexion mechanism. This pilot study will guide future research to look for potential (treatable) causes of finger flexion contractures in patients with SSc.
Methods: Grey Scale and Power Doppler ultrasound assessment of the FFTC including tendon structure and surrounding soft tissue. Measurements of the FFTC (A1 pulley, tendon and palmar plate) were made. Feasibility was assessed by the number of fingers which could be measured.
Results: We studied the second to fifth flexor tendons (n=160) of both hands in 20 patients with SSc, including early and established disease. We were able to assess the FFTC and make measurements of the flexor tendon and palmar plate in all (n=40) and A1 pulley in almost all (n=39) of the studied fingers. Common pathologies identified included peritendinous (n=12) and soft tissue (n=8) calcification. Tendon thickening was seen in 6 patients, but synovitis/tenosynovitis was rare. The A1 pulley was thickened in patients with SSc (0.46mm), in particular, those with diffuse cutaneous SSc (0.50mm).
Conclusion: We were able to successfully assess, including making measurements of, the FFTC in patients with SSc. Our study showed calcifications in the peritendinous areas and soft tissue and thickening of the A1 pulley. These findings may play a role in the pathophysiology of SSc-hand contractures by causing mechanical impingement of the finger flexion mechanism. This pilot study will guide future research to look for potential (treatable) causes of finger flexion contractures in patients with SSc.
Original language | English |
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Pages (from-to) | 77–82 |
Journal | Journal of Scleroderma and Related Disorders |
Volume | 5 |
Issue number | 1 |
Early online date | 12 Jul 2019 |
DOIs | |
Publication status | Published - 2019 |
Keywords
- Systemic sclerosis
- Scleroderma
- Ultrasound
- Flexor tendon
- Pulley
- Calcinosis
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Scleroderma and Raynaud's Research Group
Herrick, A. (PI), Dinsdale, G. (PI) & Ingram, M. (Support team)
Project: Research