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Histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot

PURPOSE: To further study the mechanism of epithelization on the fascia side of the flap after surgical incision and the treatment of the negative pressure therapy. METHODS: With the patients' informed consent, parts of tissue samples were obtained from a 51-year-old diabetic patient who was su...

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Autores principales: Dong, Jiao-Yun, Song, Fei, Qing, Chun, Lu, Shu-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555242/
https://www.ncbi.nlm.nih.gov/pubmed/28526612
http://dx.doi.org/10.1016/j.cjtee.2016.08.004
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author Dong, Jiao-Yun
Song, Fei
Qing, Chun
Lu, Shu-Liang
author_facet Dong, Jiao-Yun
Song, Fei
Qing, Chun
Lu, Shu-Liang
author_sort Dong, Jiao-Yun
collection PubMed
description PURPOSE: To further study the mechanism of epithelization on the fascia side of the flap after surgical incision and the treatment of the negative pressure therapy. METHODS: With the patients' informed consent, parts of tissue samples were obtained from a 51-year-old diabetic patient who was suffering lower extremity ulcers. The samples were processed with hematoxylin and eosin (HE) staining and Masson trichrome staining. The keratin 19, keratin 15 and carcino-embryonic antigen (CEA) were immunohistochemically detected. RESULTS: The results of HE staining showed that the specimen was divided into two regions, newborn area and original epithelial area. There were more inflammatory cells infiltrating in the dermis in the newborn epithelial area, compared with the original epithelial area. Cells in newborn epithelial area were more active and many dinuclear and polynuclear cells were observed in newborn epithelial area. But there were more cuticular layers and obvious rete pegs in original epithelial area. In addition, the cells with keratin 19 and CEA positive were found around hair follicle, while keratin 15 was negative. Masson trichrome staining showed that there was a lot of de novo collagen in newborn epithelial area. CONCLUSION: Epidermal cells on the fascia side of the flap could be derived from the stem cells. Negative pressure wound therapy would attract not only cells but also other elements such as growth factors, cytokines, some nutrients and extracellular matrix. With the formation of the appropriate microenvironment after debridement, the migrated cells can grow, differentiate and spread, eventually leading to the epithelization on the fascia side of the flap in diabetic foot.
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spelling pubmed-55552422017-08-22 Histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot Dong, Jiao-Yun Song, Fei Qing, Chun Lu, Shu-Liang Chin J Traumatol Original Article PURPOSE: To further study the mechanism of epithelization on the fascia side of the flap after surgical incision and the treatment of the negative pressure therapy. METHODS: With the patients' informed consent, parts of tissue samples were obtained from a 51-year-old diabetic patient who was suffering lower extremity ulcers. The samples were processed with hematoxylin and eosin (HE) staining and Masson trichrome staining. The keratin 19, keratin 15 and carcino-embryonic antigen (CEA) were immunohistochemically detected. RESULTS: The results of HE staining showed that the specimen was divided into two regions, newborn area and original epithelial area. There were more inflammatory cells infiltrating in the dermis in the newborn epithelial area, compared with the original epithelial area. Cells in newborn epithelial area were more active and many dinuclear and polynuclear cells were observed in newborn epithelial area. But there were more cuticular layers and obvious rete pegs in original epithelial area. In addition, the cells with keratin 19 and CEA positive were found around hair follicle, while keratin 15 was negative. Masson trichrome staining showed that there was a lot of de novo collagen in newborn epithelial area. CONCLUSION: Epidermal cells on the fascia side of the flap could be derived from the stem cells. Negative pressure wound therapy would attract not only cells but also other elements such as growth factors, cytokines, some nutrients and extracellular matrix. With the formation of the appropriate microenvironment after debridement, the migrated cells can grow, differentiate and spread, eventually leading to the epithelization on the fascia side of the flap in diabetic foot. Elsevier 2017-08 2017-04-20 /pmc/articles/PMC5555242/ /pubmed/28526612 http://dx.doi.org/10.1016/j.cjtee.2016.08.004 Text en © 2017 Production and hosting by Elsevier B.V. on behalf of Daping Hospital and the Research Institute of Surgery of the Third Military Medical University. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Dong, Jiao-Yun
Song, Fei
Qing, Chun
Lu, Shu-Liang
Histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot
title Histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot
title_full Histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot
title_fullStr Histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot
title_full_unstemmed Histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot
title_short Histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot
title_sort histomorphological observation of surgical debridement combined with negative pressure therapy in treatment of diabetic foot
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555242/
https://www.ncbi.nlm.nih.gov/pubmed/28526612
http://dx.doi.org/10.1016/j.cjtee.2016.08.004
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