2012
DOI: 10.1097/01.ehx.0000418021.80244.0f
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Histological study of the role of fat injection in scar remodeling following burn injury

Abstract: BackgroundFat grafting had been shown clinically to improve the quality of burn scars. The mechanism of fat graft survival was not clear, and the role of adipose-derived stem cells and preadipocytes in fat survival remains to be determined. Aim of the work To clinically and histologically evaluate the role of fat grafting in postburn mature scars. Patients and methodsThis study was conducted on 20 postburn mature scars. Patients' ages ranged from 18 to 38 years. Patients were selected randomly to be treated wi… Show more

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Cited by 3 publications
(2 citation statements)
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“…104 To reduce post-burn scar, fat can be injected into the scar every 8–12 weeks and repeated up to four times, significantly reducing skin hardness as measured with a Durometer and decreasing scarring assessed with the POSAS. 105 Adipose-derived stem cells are believed to underlie the positive effects on the grafted fat, 106 with preliminary work suggesting that fibroblast ECM production is altered by interactions with adipose-derived stem cells. 107 …”
Section: Non-surgical Approaches To Scar Modificationmentioning
confidence: 99%
“…104 To reduce post-burn scar, fat can be injected into the scar every 8–12 weeks and repeated up to four times, significantly reducing skin hardness as measured with a Durometer and decreasing scarring assessed with the POSAS. 105 Adipose-derived stem cells are believed to underlie the positive effects on the grafted fat, 106 with preliminary work suggesting that fibroblast ECM production is altered by interactions with adipose-derived stem cells. 107 …”
Section: Non-surgical Approaches To Scar Modificationmentioning
confidence: 99%
“…Eventually, full texts of 54 articles were assessed for eligibility. We excluded 36 studies due to: use of normal lipofilling [17][18][19][20][21][22][23][24] (nine), use in other medical conditions [25][26][27][28][29][30][31] (seven), insufficient outcome data [32,33] (three), use of an artificial material for SVF delivery [34,35] (two), inappropriate design [36][37][38] (three), non-English language [39][40][41] (three), ongoing clinical trial [42,43] (two), and use of predifferentiated cells [44] (one). In four cases [45][46][47][48] full texts were unavailable and in two [49,50] only conference abstracts were accessible.…”
Section: Search Resultsmentioning
confidence: 99%