Dear Editor, Genital involvement is frequently reported in patients with psoriasis and is associated with a major impact on quality of life (QoL) and embarrassment in engaging sexual intercourses. [1][2][3] Only 40% of patients reported to have had a previous examination of the genital area, and therefore treatment is often initiated late. 2 Genitals are considered a difficult-to-treat area. 4,5 Topical treatments remain the first-line choice for mild-to-moderate disease. 5 However, corticosteroids are associated with longterm adverse events, and specific data on immunomodulators or vitamin D derivatives are scant. Systemic treatments also have a role for moderate-to-severe disease, but evidence is mostly anecdotal also for those therapies. 4,5 Risankizumab is a humanized monoclonal antibody that blocks the p19 subunit of interleukin (IL)-23, which proved effective in clinical trials and field-practice experiences. 6,7 However, specific experiences on the treatment of genital psoriasis with risankizumab are scant and have a short follow-up. [8][9][10] We conducted a retrospective, 'real-world' study, with a 1-year follow-up, on risankizumab in the treatment of genital psoriasis. Consecutive adult (≥18 years) patients with moderate-to-severe plaque psoriasis involving the genital area and treated with risankizumab (150 mg administered subcutaneously at weeks 0, 4 and every 12 weeks thereafter) were enrolled. According to the standard protocol, assessment of effectiveness and safety was performed at baseline and after 16, 28, 40 and 52 weeks. The effectiveness of risankizumab was evaluated in terms of percentage reduction of Psoriasis Area and Severity Index (PASI) compared with baseline. In particular, the impact of the treatment on genital psoriasis was assessed by using the static Physician's Global Assessment of Genitalia (s-PGA-G), which ranges from 0 (no psoriasis) to 5 (very severe disease). 10 Safety was investigated by reporting the occurrence of any adverse events (AEs) throughout the study.In total, 93 patients were enrolled (69 males, 75%; mean age 48.2 ± 15.5 years; Table 1). The mean PASI at baseline was 19.1 ± 11.3, and 25 patients (26.9%) had severe involvement of genitalia (s-PGA-G ≥ 4). All patients completed at least 16 weeks of treatment, and 79 reached the 52-week follow-up .At baseline, the mean s-PGA-G was 3.1 ± 0.8. During the study, it decreased to 0.41 ± 0.24 at week 16, 0.21 ± 0.17