Hypertrophic scars and keloids: Overview of the evidence and practical guide for differentiating between these abnormal scars.

Grace C Limandjaja, Frank B Niessen, Rik J Scheper, Susan Gibbs
Author Information
  1. Grace C Limandjaja: Department of Molecular Cell Biology and Immunology, Amsterdam University Medical Centre (location VUmc), Vrije Universiteit Amsterdam, Amsterdam, The Netherlands. ORCID
  2. Frank B Niessen: Department of Plastic Surgery, Amsterdam University Medical Centre (location VUmc), Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  3. Rik J Scheper: Department of Pathology, Amsterdam University Medical Centre (location VUmc), Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  4. Susan Gibbs: Department of Molecular Cell Biology and Immunology, Amsterdam University Medical Centre (location VUmc), Vrije Universiteit Amsterdam, Amsterdam, The Netherlands. ORCID

Abstract

Although hypertrophic scars and keloids both generate excessive scar tissue, keloids are characterized by their extensive growth beyond the borders of the original wound, which is not observed in hypertrophic scars. Whether or not hypertrophic scars and keloids are two sides of the same coin or in fact distinct entities remains a topic of much debate. However, proper comparison between the two ideally occurs within the same study, but this is the exception rather than the rule. For this reason, the goal of this review was to summarize and evaluate all publications in which both hypertrophic scars and keloids were studied and compared to one another within the same study. The presence of horizontal growth is the mainstay of the keloid diagnosis and remains the strongest argument in support of keloids and hypertrophic scars being distinct entities, and the histopathological distinction is less straightforward. Keloidal collagen remains the strongest keloid parameter, but dermal nodules and α-SMA immunoreactivity are not limited to hypertrophic scars alone. Ultimately, the current hypertrophic scars-keloid differences are mostly quantitative in nature rather than qualitative, and many similar abnormalities exist in both lesions. Nonetheless, the presence of similarities does not equate the absence of fundamental differences, some of which may not yet have been uncovered given how much we still have to learn about the processes involved in normal wound healing. It therefore seems pertinent to continue treating hypertrophic scars and keloids as separate entities, until such a time as new findings more decisively convinces us otherwise.

Keywords

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MeSH Term

Actins
Cicatrix, Hypertrophic
Collagen
Diagnosis, Differential
Humans
Keloid

Chemicals

ACTA2 protein, human
Actins
Collagen

Word Cloud

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