[libribook.com] Traumatic Scar Tissue Management 1st Edition

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Clinical presentationExpanded dermiscomprises flatter andless clearly demarcated,loosely arrayed wavycollagen bundles thatare somewhatfragmented andshortened and displayprominent verticallyoriented blood vesselsHard, usually linear,slightly-raised scar withwell demarcatedepidermal borders (donot extend beyond thegeneral geographicwound margins)Appears red or pink incolorCommonly pruritic*Keloidal collagen is not always detectable in KSs.collagen swirls andwhorls that vary inlengthNumerous, thickenedfibrocollagenousfasciclesHorizontal fibrousbands in the upperreticular dermis andthe presence ofprominent fascia-likebandsFirm, mildly tender,bosselated & moreraised than HSs, witha shiny surface &occasionaltelangiectasia,infiltrates thesurrounding tissue,well demarcated,irregular bordersThinned epithelium isprone to ulceration,hyperpigmentationand discoloration(pink/purple – initiallyerythematous, turningbrownish, may pale asthe scar ages)Scar margins tend toexhibit considerableperipheral tensionwhereas center of thescar less soCan cause significantpain andhyperesthesiaRaised above skin surfaceDiscolorationPain, pruritus, adherencesand contractures can affectquality of life: physically,physiologically andpsychologicallyDisfigurements presentbiopsychosocialconsiderations

Table 6.1Comparison of scars (Ogawa 2008, Bordoni & Zanier 2013, Bordoni & Zanier 2013, Zhu et al.2013, Rabello et al. 2014)Hypertrophic scarring can result in disfigurement and scarring that affectsquality of life which, in turn, can lead to lowered self-esteem, social isolation,prejudicial societal reactions and job discrimination. Scarring also has profoundrehabilitation consequences, including loss of function, impairment, disability,and difficulties pursuing recreational and vocational pursuits (Engrav et al.2007).Bacterial colonization and wound infection tend to promote the formation ofhypertrophic scars (Niessen et al. 2004, Chan et al. 2005, Baker et al. 2007,Berman et al. 2007, Cho et al. 2014). Hypertrophic scarring usually developswithin 1–3 months following wound infection, wound closure with excesstension or other traumatic skin injury (Brissett & Sherris 2001, Cho et al. 2014).Hypertrophic scarring exhibits a rapid growth phase for up to 6 months, and thengradually regresses over a period of a few years.Keloids seem to be a more sustained and aggressive fibrotic disorder thanhypertrophic scars (Brown & Bayat 2009). Research to date strongly suggests amore prolonged inflammatory period, with immune cell infiltrate present withkeloids (Slemp & Kirschner 2006).Precise etiologic factors associated with keloid formation are elusive. Keloidsmay develop anywhere from a year up to several years after minor injuries andmay even form spontaneously on the mid-chest in the absence of any knowninjury (Brissett & Sherris 2001, Cho et al. 2014). Keloids are persistent and donot regress spontaneously.Keloids appear as firm, mildly tender, bosselated (small knob-like projections)tumors with a shiny surface and sometimes telangiectasia (small, widened bloodvessels on the skin which are usually meaningless, but may be associated withseveral diseases) (NIH 2015). The epithelium is thinned and there may be focalareas of ulceration.

Table 6.1

Comparison of scars (Ogawa 2008, Bordoni & Zanier 2013, Bordoni & Zanier 2013, Zhu et al.

2013, Rabello et al. 2014)

Hypertrophic scarring can result in disfigurement and scarring that affects

quality of life which, in turn, can lead to lowered self-esteem, social isolation,

prejudicial societal reactions and job discrimination. Scarring also has profound

rehabilitation consequences, including loss of function, impairment, disability,

and difficulties pursuing recreational and vocational pursuits (Engrav et al.

2007).

Bacterial colonization and wound infection tend to promote the formation of

hypertrophic scars (Niessen et al. 2004, Chan et al. 2005, Baker et al. 2007,

Berman et al. 2007, Cho et al. 2014). Hypertrophic scarring usually develops

within 1–3 months following wound infection, wound closure with excess

tension or other traumatic skin injury (Brissett & Sherris 2001, Cho et al. 2014).

Hypertrophic scarring exhibits a rapid growth phase for up to 6 months, and then

gradually regresses over a period of a few years.

Keloids seem to be a more sustained and aggressive fibrotic disorder than

hypertrophic scars (Brown & Bayat 2009). Research to date strongly suggests a

more prolonged inflammatory period, with immune cell infiltrate present with

keloids (Slemp & Kirschner 2006).

Precise etiologic factors associated with keloid formation are elusive. Keloids

may develop anywhere from a year up to several years after minor injuries and

may even form spontaneously on the mid-chest in the absence of any known

injury (Brissett & Sherris 2001, Cho et al. 2014). Keloids are persistent and do

not regress spontaneously.

Keloids appear as firm, mildly tender, bosselated (small knob-like projections)

tumors with a shiny surface and sometimes telangiectasia (small, widened blood

vessels on the skin which are usually meaningless, but may be associated with

several diseases) (NIH 2015). The epithelium is thinned and there may be focal

areas of ulceration.

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