摘要
Objectives: To investigate the efficacy of epidermal noncultured cellular grafting in patients with vitiligo and the role of postinflammatory, spontaneous, or UV-induced pigmentation in obtaining repigmentation. Design: A prospective, randomized, double-blind, placebo-controlled study. Setting: Ambulatory patients in an institutional practice. Patients were followed up for 3 to 12 months. Patients: A total of 33 paired, symmetrically distributed leukodermic lesions, all resistant to therapy, were observed in 28 patients. Nineteen patients appeared to have a stable vitiligo (group 1), whereas there was doubt about the stability of the disease in 9 patients (group 2). Intervention: After laser ablation, a hyaluronic acid-enriched cellular graft was applied to 1 lesion while the paired lesion received placebo. Three weeks later all lesions were exposed to UV irradiation twice per week for approximately 2 months. Main Outcome Measures: Primarily, the percentage of repigmentationwas assessed after 3, 6, and 12months using a digital image analysis system. The repigmentation patternwas also evaluated after 1 and 3 months. Results: A strongly significant difference between cellular grafts and placebo was observed after 3, 6, and 12 months (P < .001, P=.002, and P=.002, respectively). In group 1, repigmentation of at least 70%of the treated area was achieved in 55%, 57%, and 77%of the actively treated lesions 3, 6, and 12 months after treatment, whereas in group 2 repigmentation of at least 70%of the treated area was not observed at any time point. The repigmentation pattern was diffuse in 94%of the responding patients. Conclusions: After a strict preoperative selection for disease stability, transplantation resulted in repigmentation of at least 70%of the treated area in most actively treated vitiligo lesions. Repigmentation was primarily caused by the transplanted melanocytes.
Objectives: To investigate the efficacy of epidermal noncultured cellular grafting in patients with vitiligo and the role of postinflammatory, spontaneous, or UV-induced pigmentation in obtaining repigmentation. Design: A prospective, randomized, double-blind, placebo-controlled study. Setting: Ambulatory patients in an institutional practice. Patients were followed up for 3 to 12 months. Patients: A total of 33 paired, symmetrically distributed leukodermic lesions, all resistant to therapy, were observed in 28 patients. Nineteen patients appeared to have a stable vitiligo (group 1), whereas there was doubt about the stability of the disease in 9 patients (group 2). Intervention: After laser ablation, a hyaluronic acid-enriched cellular graft was applied to 1 lesion while the paired lesion received placebo. Three weeks later all lesions were exposed to UV irradiation twice per week for approximately 2 months. Main Outcome Measures: Primarily, the percentage of repigmentationwas assessed after 3, 6, and 12months using a digital image analysis system. The repigmentation patternwas also evaluated after 1 and 3 months. Results: A strongly significant difference between cellular grafts and placebo was observed after 3, 6, and 12 months (P < .001, P=.002, and P=.002, respectively). In group 1, repigmentation of at least 70%of the treated area was achieved in 55%, 57%, and 77%of the actively treated lesions 3, 6, and 12 months after treatment, whereas in group 2 repigmentation of at least 70%of the treated area was not observed at any time point. The repigmentation pattern was diffuse in 94%of the responding patients. Conclusions: After a strict preoperative selection for disease stability, transplantation resulted in repigmentation of at least 70%of the treated area in most actively treated vitiligo lesions. Repigmentation was primarily caused by the transplanted melanocytes.
