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Effects of local phenytoin on seroma formation after mastectomy and Axillary lymph node dissection: an experimental study on mice
BACKGROUND: Seroma formation is the most common complication after breast cancer surgery. It is an important complication since it prolongs therapy duration, increases cost, and negatively affects patient psychology. Currently, there is no widely accepted method that prevents seroma formation. We tr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563462/ https://www.ncbi.nlm.nih.gov/pubmed/23253781 http://dx.doi.org/10.1186/1471-2482-12-25 |
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author | Eser, Mehmet Tutal, Fırat Kement, Metin Goktas, Selcuk Kaptanoglu, Levent Gökceimam, Mehmet Gecer, Melin Ozgun Uzun, Huseyin |
author_facet | Eser, Mehmet Tutal, Fırat Kement, Metin Goktas, Selcuk Kaptanoglu, Levent Gökceimam, Mehmet Gecer, Melin Ozgun Uzun, Huseyin |
author_sort | Eser, Mehmet |
collection | PubMed |
description | BACKGROUND: Seroma formation is the most common complication after breast cancer surgery. It is an important complication since it prolongs therapy duration, increases cost, and negatively affects patient psychology. Currently, there is no widely accepted method that prevents seroma formation. We tried to investigate impact of local phenytoin application on seroma formation following an experimental mastectomy model created in rats. METHODS: Two groups including eight rats in each were randomized. Saline injection was applied in the first group, whereas 1% phenytoin was locally used in the second group. Ten days after the surgery, seroma formation and wound-healing processes were evaluated using histopathological and biochemical examinations. RESULTS: Phenytoin significantly decreased seroma formation. Fibrosis was significantly increased and angiogenesis was significantly reduced in the phenytoin group (P < 0.05). Increased levels of macrophage and lymphocyte infiltration was detected in the control group (P < 0.05). No difference was detected between the groups in terms of necrosis, edema, congestion, and PNL (Polymorphonuclear leucocyte) and fibroblast infiltration. CONCLUSIONS: Seroma formation-reducing effect of phenytoin might have occurred over its anti-inflammatory, anti-angiogenetic, and fibrosis augmenting effects. |
format | Online Article Text |
id | pubmed-3563462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35634622013-02-08 Effects of local phenytoin on seroma formation after mastectomy and Axillary lymph node dissection: an experimental study on mice Eser, Mehmet Tutal, Fırat Kement, Metin Goktas, Selcuk Kaptanoglu, Levent Gökceimam, Mehmet Gecer, Melin Ozgun Uzun, Huseyin BMC Surg Research Article BACKGROUND: Seroma formation is the most common complication after breast cancer surgery. It is an important complication since it prolongs therapy duration, increases cost, and negatively affects patient psychology. Currently, there is no widely accepted method that prevents seroma formation. We tried to investigate impact of local phenytoin application on seroma formation following an experimental mastectomy model created in rats. METHODS: Two groups including eight rats in each were randomized. Saline injection was applied in the first group, whereas 1% phenytoin was locally used in the second group. Ten days after the surgery, seroma formation and wound-healing processes were evaluated using histopathological and biochemical examinations. RESULTS: Phenytoin significantly decreased seroma formation. Fibrosis was significantly increased and angiogenesis was significantly reduced in the phenytoin group (P < 0.05). Increased levels of macrophage and lymphocyte infiltration was detected in the control group (P < 0.05). No difference was detected between the groups in terms of necrosis, edema, congestion, and PNL (Polymorphonuclear leucocyte) and fibroblast infiltration. CONCLUSIONS: Seroma formation-reducing effect of phenytoin might have occurred over its anti-inflammatory, anti-angiogenetic, and fibrosis augmenting effects. BioMed Central 2012-12-19 /pmc/articles/PMC3563462/ /pubmed/23253781 http://dx.doi.org/10.1186/1471-2482-12-25 Text en Copyright ©2012 Eser et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Eser, Mehmet Tutal, Fırat Kement, Metin Goktas, Selcuk Kaptanoglu, Levent Gökceimam, Mehmet Gecer, Melin Ozgun Uzun, Huseyin Effects of local phenytoin on seroma formation after mastectomy and Axillary lymph node dissection: an experimental study on mice |
title | Effects of local phenytoin on seroma formation after mastectomy and Axillary lymph node dissection: an experimental study on mice |
title_full | Effects of local phenytoin on seroma formation after mastectomy and Axillary lymph node dissection: an experimental study on mice |
title_fullStr | Effects of local phenytoin on seroma formation after mastectomy and Axillary lymph node dissection: an experimental study on mice |
title_full_unstemmed | Effects of local phenytoin on seroma formation after mastectomy and Axillary lymph node dissection: an experimental study on mice |
title_short | Effects of local phenytoin on seroma formation after mastectomy and Axillary lymph node dissection: an experimental study on mice |
title_sort | effects of local phenytoin on seroma formation after mastectomy and axillary lymph node dissection: an experimental study on mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563462/ https://www.ncbi.nlm.nih.gov/pubmed/23253781 http://dx.doi.org/10.1186/1471-2482-12-25 |
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