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DOI 10.1046/j.1524-4725.2001.01045.x

Медицинская библиотека · Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.] · 2001

Modified technique of autologous noncultured epidermal cell transplantation for repigmenting vitiligo: a pilot study.

van Geel N, Ongenae K, De Mil M, Naeyaert J M

Клинический случайСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

Several reports have demonstrated that grafting of autologous melanocytes from normally pigmented donor skin can be used for repigmentation of achromic macules in vitiligo.

OBJECTIVE

To investigate a modified approach in which noncultured autologous melanocytes and keratinocytes are grafted on superficially laser dermabraded vitiligo lesions in a suspension enriched with hyaluronic acid.

METHODS

Four patients with stable vitiligo were treated using a noncultured melanocyte-keratinocyte suspension. The cellular suspension was grafted on vitiliginous lesions previously dermabraded with a CO2 laser. To improve the viscosity and fixation of the cellular suspension hyaluronic acid was added. Three weeks after grafting, psoralen plus ultraviolet A (PUVA) or ultraviolet B (UVB) therapy was started. Residual leukodermic areas were subsequently retreated.

RESULTS

Repigmentation was observed within 2-4 weeks and continued to increase for 3 months after treatment. In all patients, 85-100% repigmentation was achieved. A temporary slight color mismatch was visible in all patients. The most homogeneous repigmentation was obtained 5 months after treatment.

CONCLUSION

This modified procedure seems to be a simple and promising treatment for larger vitiliginous areas.

Для цитирования: van Geel N, Ongenae K, De Mil M, Naeyaert J M. Modified technique of autologous noncultured epidermal cell transplantation for repigmenting vitiligo: a pilot study.. Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]. 2001. DOI: 10.1046/j.1524-4725.2001.01045.x.

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