[libribook.com] Traumatic Scar Tissue Management 1st Edition
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.
- Page 452 and 453: Pathophysiological considerationFib
- Page 454 and 455: Table 5.2Important pathophysiologic
- Page 456 and 457: According to Klingler (2012):… pa
- Page 458 and 459: Table 5.3Scar types and related ter
- Page 460 and 461: unyielding or pliable and mobile. R
- Page 462 and 463: Prolonged InflammationInflammation
- Page 464 and 465: ImmobilizationThe impact of immobil
- Page 467 and 468: Figure 5.4The fall-out associated w
- Page 469 and 470: Clinical ConsiderationHere we see t
- Page 471 and 472: Pathophysiological ConsiderationAcc
- Page 473 and 474: Pathophysiological ConsiderationNeu
- Page 475 and 476: The diverse biological effects of N
- Page 477 and 478: Clinical ConsiderationCareful appli
- Page 479 and 480: Clinical ConsiderationSome patholog
- Page 481 and 482: Pathophysiological ConsiderationSom
- Page 483 and 484: compressive effect in the keloidal
- Page 485 and 486: alterations in the mechanical envir
- Page 487 and 488: Clinical ConsiderationMechanical fo
- Page 489 and 490: Table 5.4Role of neuropeptides (NP)
- Page 491 and 492: Fitch P (2005) Scars of life. Journ
- Page 493 and 494: Langevin HM (2006) Connective tissu
- Page 495 and 496: active scars. Journal of Bodywork a
- Page 497 and 498: trauma.
- Page 499 and 500: Clinical ConsiderationPostsurgical
- Page 501: following burn injury,bacterial col
- Page 505 and 506: Pathophysiological ConsiderationAcc
- Page 507 and 508: BurnsA burn injury to the skin or o
- Page 510 and 511: Figure 6.1Depth of burn trauma and
- Page 512 and 513: • Stimulate ECM formation• Regu
- Page 514 and 515: Clinical ConsiderationIt has been i
- Page 516 and 517: Clinical ConsiderationMT may be a v
- Page 518 and 519: ThermoregulationThermoregulation (t
- Page 520 and 521: from the tissues and taken up by th
- Page 522 and 523: treatment strategies are difficult
- Page 524 and 525: Clinical ConsiderationSkin rolling
- Page 526 and 527: Sequelae and ComplicationsAdvances
- Page 528 and 529: • Paresthesia - 47%• Arm/should
- Page 530 and 531: breast or around the edge of the ar
- Page 532 and 533: Radiation scarringScar tissue as a
- Page 534 and 535: Implants and painPain of fluctuatin
- Page 536 and 537: LymphedemaBreast cancer treatment o
- Page 538 and 539: volume of fluid that accumulates or
- Page 540 and 541: OneTwoThreeCommonly referred to as
- Page 542 and 543: myokinetic chain/myofascial meridia
- Page 544: • Loss of touch sensation• Clum
- Page 548 and 549: Figure 6.3Distribution of nerves in
- Page 550 and 551: include preservation of as much of
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.