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Journal of plastic, reconstructive & aesthetic surgery, 2019-01, Vol.72 (1), p.4-11
2019
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Details

Autor(en) / Beteiligte
Titel
Treatment of keloid scars with intralesional triamcinolone and 5-fluorouracil injections – a randomized controlled trial
Ist Teil von
  • Journal of plastic, reconstructive & aesthetic surgery, 2019-01, Vol.72 (1), p.4-11
Ort / Verlag
Netherlands: Elsevier Ltd
Erscheinungsjahr
2019
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Keloids have high recurrence rates. Current first-line therapy is triamcinolone (TAC) injection, but it has been suggested that approximately 50% of keloids are steroid resistant. We compared the efficacy of intralesional 5-fluorouracil (5-FU) and triamcinalone injections in a double-blind randomized controlled trial. Forty-three patients with 50 keloid scars were treated with either intralesional TAC or 5-FU-injections over 6 months. There was no statistically significant difference in the remission rate at 6 months between the 5-FU and TAC groups (46% vs 60%, respectively). Local adverse effects were higher in the TAC group compared to the 5-FU group. Occurrence of skin atrophy in TAC group was 44% and in the 5-FU group 8% (p < 0.05). Also the occurrence of telangiectasia in the TAC group was 50% and in the 5-FU 21% (p < 0.05). Vascularity of the keloids, assessed by spectral imaging and immunohistochemical staining for blood vessels, after treatment decreased in the TAC group, but not in the 5-FU group (p < 0.05). Fibroblast proliferation evaluated by Ki-67 staining significantly decreased in the TAC group (p < 0.05) but increased in the 5-FU group (p < 0.05). TAC and 5-FU injections did not differ in their clinical effectivity in this randomized study, but 5-FU injections lead to increased proliferation rate and did not affect vascular density in histological assessment. Due to the greater number of adverse effects observed after TAC treatment, 5-FU injections may be preferable for cosmetically sensitive skin areas.
Sprache
Englisch
Identifikatoren
ISSN: 1748-6815
eISSN: 1878-0539
DOI: 10.1016/j.bjps.2018.05.052
Titel-ID: cdi_proquest_miscellaneous_2135635418

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