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Clinical and Histological Correlation in Post-Burn Hypertrophic Scar for Pain and Itching Sensation

BACKGROUND: Hypertrophic scar following a burn is caused by the excessive deposit of collagen resulting in an exaggerated wound healing response. The burn patient complains of pain and itching over the scar, which can give rise to cosmetic and functional problems. OBJECTIVE: The aim of this study wa...

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Autores principales: Choi, Young-Hee, Kim, Kwang-Min, Kim, Hye-One, Jang, Young-Chul, Kwak, In-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870210/
https://www.ncbi.nlm.nih.gov/pubmed/24371389
http://dx.doi.org/10.5021/ad.2013.25.4.428
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author Choi, Young-Hee
Kim, Kwang-Min
Kim, Hye-One
Jang, Young-Chul
Kwak, In-Suk
author_facet Choi, Young-Hee
Kim, Kwang-Min
Kim, Hye-One
Jang, Young-Chul
Kwak, In-Suk
author_sort Choi, Young-Hee
collection PubMed
description BACKGROUND: Hypertrophic scar following a burn is caused by the excessive deposit of collagen resulting in an exaggerated wound healing response. The burn patient complains of pain and itching over the scar, which can give rise to cosmetic and functional problems. OBJECTIVE: The aim of this study was to investigate the clinical and histological correlation of a hypertrophic burn scar for itching and pain sensations. METHODS: Thirty-eight patients underwent a scar release and skin graft. the modified Vancouver scar scale and the verbal numerical rating scale were recorded. All biopsies were taken from scar tissue (scar) and normal tissue (normal). Histologically, tissues were observed in the epidermis, the monocytes around the vessels, the collagen fiber, elastic fiber, and the mast cells. RESULTS: The mean total score of MVSS was 8.4±2.7 (pliability 2.0±0.9; thickness 1.8±0.9; vascularity 2.0± 0.9; and pigmentation 2.1±0.9). Pain and itching were 2.4±2.0 and 2.9±3.0. Epidermis were 7.9±2.8 layers (scar) and 4.0±0.8 layers (normal). The collagen fibers were thin and dense (scar) and thicker and loose (normal). The elastic fibers were thin and nonexistent (scar) and thin and loose (normal). Mast cells were 11.2±5.8/high power field (scar) and 7.4±4.1 (normal). CONCLUSION: As the scar tissue thickens, the itching becomes more severe. The stiffness of the scar with the pain appeared to be associated with the condition of the tissue. The correlation between clinical and histological post-burn hypertrophic scars will help further studies on the scar. This helped with the development of the base material for therapeutic strategies.
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spelling pubmed-38702102013-12-26 Clinical and Histological Correlation in Post-Burn Hypertrophic Scar for Pain and Itching Sensation Choi, Young-Hee Kim, Kwang-Min Kim, Hye-One Jang, Young-Chul Kwak, In-Suk Ann Dermatol Original Article BACKGROUND: Hypertrophic scar following a burn is caused by the excessive deposit of collagen resulting in an exaggerated wound healing response. The burn patient complains of pain and itching over the scar, which can give rise to cosmetic and functional problems. OBJECTIVE: The aim of this study was to investigate the clinical and histological correlation of a hypertrophic burn scar for itching and pain sensations. METHODS: Thirty-eight patients underwent a scar release and skin graft. the modified Vancouver scar scale and the verbal numerical rating scale were recorded. All biopsies were taken from scar tissue (scar) and normal tissue (normal). Histologically, tissues were observed in the epidermis, the monocytes around the vessels, the collagen fiber, elastic fiber, and the mast cells. RESULTS: The mean total score of MVSS was 8.4±2.7 (pliability 2.0±0.9; thickness 1.8±0.9; vascularity 2.0± 0.9; and pigmentation 2.1±0.9). Pain and itching were 2.4±2.0 and 2.9±3.0. Epidermis were 7.9±2.8 layers (scar) and 4.0±0.8 layers (normal). The collagen fibers were thin and dense (scar) and thicker and loose (normal). The elastic fibers were thin and nonexistent (scar) and thin and loose (normal). Mast cells were 11.2±5.8/high power field (scar) and 7.4±4.1 (normal). CONCLUSION: As the scar tissue thickens, the itching becomes more severe. The stiffness of the scar with the pain appeared to be associated with the condition of the tissue. The correlation between clinical and histological post-burn hypertrophic scars will help further studies on the scar. This helped with the development of the base material for therapeutic strategies. Korean Dermatological Association; The Korean Society for Investigative Dermatology 2013-11 2013-11-30 /pmc/articles/PMC3870210/ /pubmed/24371389 http://dx.doi.org/10.5021/ad.2013.25.4.428 Text en Copyright © 2013 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Young-Hee
Kim, Kwang-Min
Kim, Hye-One
Jang, Young-Chul
Kwak, In-Suk
Clinical and Histological Correlation in Post-Burn Hypertrophic Scar for Pain and Itching Sensation
title Clinical and Histological Correlation in Post-Burn Hypertrophic Scar for Pain and Itching Sensation
title_full Clinical and Histological Correlation in Post-Burn Hypertrophic Scar for Pain and Itching Sensation
title_fullStr Clinical and Histological Correlation in Post-Burn Hypertrophic Scar for Pain and Itching Sensation
title_full_unstemmed Clinical and Histological Correlation in Post-Burn Hypertrophic Scar for Pain and Itching Sensation
title_short Clinical and Histological Correlation in Post-Burn Hypertrophic Scar for Pain and Itching Sensation
title_sort clinical and histological correlation in post-burn hypertrophic scar for pain and itching sensation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870210/
https://www.ncbi.nlm.nih.gov/pubmed/24371389
http://dx.doi.org/10.5021/ad.2013.25.4.428
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