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Lower-limb ulcers in systemic sclerosis patients are rarely reported. The aim of this study was to describe the main causes and outcomes of lower-limb ulcers in systemic sclerosis patients and to assess factors associated with ischaemic causes (arterial disease and/or microvascular impairment). A retrospective, multicentre, case-control study was conducted in 2013 and 2014, including 45 systemic sclerosis patients presenting lower-limb ulcers between 2008 and 2013. The estimated prevalence of lower-limb ulcers among systemic sclerosis patients was 12.8%. Ulcers were related to venous insufficiency in 22 cases (49%), ischaemic causes in 21 (47%) and other causes in 2 (4%). Complete healing was observed in 60% of cases in a mean time of 10.3 months; 59% relapsed during a mean follow-up of 22 months. Ischaemic lower-limb ulcer outcomes were poor, with a 28.6% amputation rate. Logistic-regression multivariate analyses between ischaemic lower-limb ulcer cases and matched systemic sclerosis-controls identified past or concomitant digital ulcer and cutaneous sclerosis of the feet as independent risk factors associated with ischaemic lower-limb ulcers.

International audience; Pruritus is a frequent symptom in systemic sclerosis (SSc), with a prevalence of 40-65%, but its pathophysiology is poorly understood. This study investigated the immunological component of pruritus. Fifty-six patients with SSc responded to a standardized questionnaire regarding both SSc disease and pruritus characteristics. Among patients with SSc, those with pruritus did not display a particular immunological profile (inflammatory, humoral, and/or cellular factors), but pruritus was, in most cases, concomitant with the development of SSc. Thus, pruritus characteristics were evaluated further, according to the detection of anti-centromere autoantibodies (ACA), into ACA+ (n = 17) and ACA- (n = 19). The ACA+ subgroup was characterized by a longer evolution of SSc and pruritus, pruritus present outside the sclerotic area, and a shorter daily duration of pruritus. In conclusion, the concomitant appearance of the 2 processes and the differences observed between ACA+ and ACA- subgroups support the presence of an immunological component in pruritus.

The efficacy and safety of botulinum toxin B (BTX-B) for treatment of Raynaud's phenomenon and digital ulcers in patients with systemic sclerosis was assessed. A total of 45 patients with systemic sclerosis who had Raynaud's phenomenon were blinded and divided randomly into 4 groups: a no-treatment control group, and 3 treatment groups, using 250, 1,000 or 2,000 international units (U) of BTX-B injections in the hand with more severe symptoms. Four weeks after injection, pain/numbness visual analogue scale scores and Raynaud's score in the groups treated with 1,000 and 2,000 U BTX-B were significantly lower than in the control group and the group treated with 250 U BTX-B. These beneficial effects were sustained until 16 weeks after the single injection. At 4 weeks after injection skin temperature recovery in the group treated with 2,000 U BTX-B was significantly improved. The numbers of digital ulcers in the groups treated with 1,000 and 2,000 U BTX-B were significantly lower than in the control group. In conclusion, 1,000 and 2,000 U BTX-B injections significantly suppressed the activity of Raynaud's phenomenon and digital ulcers in patients with SSc without serious adverse events.

Systemic sclerosis (SSc) is a connective tissue disorder characterized by the fibrosis in the skin and internal organs. SSc is characterized by the presence of autoantibodies that are produced by B lymphocytes. Recently, the importance of B lymphocytes in immune response and autoimmunity has been recognized. CD19, which is a critical cell-surface signal transduction molecule of B cells, positively regulates signaling through B cell antigen receptor and controls autoantibody production. B cells from SSc patients exhibit CD19 overexpression that results in disturbed peripheral B cell homeostasis characterized by increased naive B cells and decreased but activated memory B cells. These findings indicate that B cells are potential therapeutic targets in SSc. Since SSc is a heterogeneous disorder, the subset classification of limited cutaneous SSc and diffuse cutaneous SSc (dSSc) is critical for predicting prognosis and selecting appropriate treatment. Although none of drugs have been proved to be effective for SSc by controlled studies, there are some therapeutic choices that may be effective for patients with early dSSc. Oral low-dose steroid is frequently effective for skin sclerosis, when it is used for early dSSc patients with edematous and rapidly progressing skin fibrosis. Many uncontrolled trials have shown that treatment with cyclophosphamide plus steroid may be effective for SSc patients with active alveolitis. Since it is difficult to remove fibrosis once established in SSc, it should be emphasized that early diagnosis and early treatment of dSSc are critical for management of SSc., Acta medica Nagasakiensia. 2006, 51(1), p.1-7