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Dermatology Times
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This week’s collection of the latest dermatologic studies includes the impact of isotretinoin treatment on femoral cartilage thickness, cystic fibrosis dermatitis arthritis syndrome, the role of intratumoral therapies for cutaneous melanoma, and fractional pigment toning for treating benign epidermal pigmented lesions.
Kulakli et al evaluated the impact of isotretinoin treatment on femoral cartilage thickness (FCT) in patients with acne and explored its potential as a risk factor for developing osteoarthritis (OA). The study included 52 patients with acne and 45 healthy controls, with ultrasound measurements of FCT before and after treatment. Kulakli et al’s results demonstrated a significant increase in FCT in multiple knee regions after isotretinoin treatment, suggesting possible early cartilage changes. However, no direct correlation was found between treatment duration, cumulative dose, and FCT changes. According to the study authors, their findings suggest that isotretinoin may trigger early OA-like changes in cartilage, particularly in young patients. However, further studies with longer follow-ups are needed.1
In their study, Schwartzman et al described a newly recognized condition termed cystic fibrosis dermatitis arthritis syndrome (CF-DAS), characterized by episodic skin eruptions and arthritis in cystic fibrosis (CF) patients. The study focused on 4 female patients, aged 9 to 26, who exhibited recurrent pink papules, plaques, and nodules, lasting 5 to 7 days, primarily on the extremities. The patients’ episodes were associated with severe arthralgias and, in some cases, arthritis. Histopathological findings varied, showing neutrophilic infiltrates and small vessel vasculitis. All 4 patients were treated with supportive nonsteroidal anti-inflammatory drugs, and one patient showed significant improvement with oral dapsone. Schwartzman et al’s study suggests that CF-DAS may be immunologically driven, potentially linked to immune complex deposition, and emphasizes the importance of recognizing CF-DAS to avoid misdiagnosis and inappropriate treatment. According to the authors, CF-DAS is distinct from other similar dermatologic and rheumatologic disorders and does not correlate with pulmonary exacerbations.2
Katz et al explored the efficacy and safety of various intratumoral (IT) therapies for treating cutaneous melanoma, particularly in cases where surgery or radiation is not viable. IT therapy involves directly injecting therapeutic agents into tumors to achieve local control and potentially stimulate systemic antitumor responses while minimizing systemic toxicity. Katz et al’s review covers several novel IT agents, including immune-enhancing agents such as pembrolizumab and ipilimumab, oncolytic viruses such as talimogene laherparepvec (T-VEC) and coxsackievirus A21, and non-immunologic agents such as rose bengal (PV-10). The study author’s results show that IT therapies offer promising outcomes in terms of overall response rates (ORR) and durability, with a generally favorable safety profile. T-VEC and CVA21 showed notable efficacy, particularly when combined with systemic immunotherapies. According to Katz et al, their study emphasizes the potential of IT therapies as an alternative or adjunct to systemic treatments.3
Manuskiatti et al’s study evaluated a new laser technique of fractional pigment toning (FPT) for treating benign epidermal pigmented lesions in patients with darker skin tones. A total of 27 patients with solar lentigines underwent treatment using both FPT and a conventional technique (CT) on different sides of the face. The study found that both techniques effectively reduced pigmentation, but FPT resulted in less post-inflammatory hyperpigmentation (PIH) and faster recovery. PIH incidence was significantly higher with the CT approach, reaching 96% at 3 months post-treatment, compared to milder and less widespread PIH with FPT. Although FPT caused more treatment discomfort, it offered comparable or better pigment clearance and fewer adverse effects, suggesting its potential as a safer, more effective option for patients at risk of PIH, according to Manuskiatti et al.4
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