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DOI 10.1097/dss.0000000000004566

Медицинская библиотека · Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.] · 2025

Intralesional Insulin Is Superior to Intralesional Botulinum Toxin-A in the Treatment of Keloids.

Elradi Mona, Selim Heba, Hamed Dina E

СтатьяРандомизированное исследованиеСравнительное исследованиеПеревод в очереди

Аннотация

BACKGROUND

Keloids represent a troublesome condition that lacks a proper standard management protocol. Insulin and botulinum toxin A (BTX-A) both have evidence-based anti-scarring effects. Hence, their role in treating keloids needs to be investigated.

OBJECTIVE

To compare insulin's efficacy versus BTX-A in treating keloids.

PATIENTS AND

METHODS

Sixty-three patients with keloids were randomly allocated into 3 equal groups. Group A was treated with intralesional insulin, Group B with intralesional BTX-A, and Group C with intralesional corticosteroids, each for 4 monthly sessions. The results were assessed objectively and subjectively using the patient and observer scar assessment scale.

RESULTS

All 3 groups showed a statistically significant reduction in volume before and after therapy, with percent changes of 66.6%, 25.3%, and 75% for Groups A, B, and C, respectively. Insulin and corticosteroids were statistically superior to BTX-A in improving pigmentation, reducing thickness, and inducing relief in treated keloids.

CONCLUSION

Both insulin and BTX-A show a promising role in managing keloids, with insulin demonstrating better efficacy. Botulinum toxin A is better recommended as an adjuvant therapy alongside other mainstay treatment modalities. Larger-scale studies are needed to confirm their roles and establish guidelines for their use.

Для цитирования: Elradi Mona, Selim Heba, Hamed Dina E. Intralesional Insulin Is Superior to Intralesional Botulinum Toxin-A in the Treatment of Keloids.. Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]. 2025. DOI: 10.1097/dss.0000000000004566.

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