<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">FMAR</journal-id><journal-title-group><journal-title>Forensic Medicine and Anatomy Research</journal-title></journal-title-group><issn pub-type="epub">2327-4115</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/fmar.2016.41001</article-id><article-id pub-id-type="publisher-id">FMAR-61999</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Time Course of Histomorphologic Features during Chronic Burn Wound Healing
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>asser</surname><given-names>S. El-Sayed</given-names></name><xref ref-type="aff" rid="aff1"><sub>1</sub></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>Department of Veterinary Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Damanhour 
University, Damanhour, Egypt</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>yasserelsayed75@gmail.com</email></corresp></author-notes><pub-date pub-type="epub"><day>17</day><month>12</month><year>2015</year></pub-date><volume>04</volume><issue>01</issue><fpage>1</fpage><lpage>6</lpage><history><date date-type="received"><day>30</day>	<month>October</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>14</month>	<year>December</year>	</date><date date-type="accepted"><day>17</day>	<month>December</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  In forensic pathology, it is always indispensable to determine burn wound vitality or age to accurately assess the relationship between death and any burn wounds. Subsequently, the determination of wound age is a definitive and still cutting-edge subject in forensic pathology. Therefore, deep second-degree burn injuries were induced in a group of mice. At 7, 12, 17, 21 and 28 days post-burn, burn wound specimens were histomorphologically differentiated and compared with normal intact skin using H&amp;E stain. The study revealed that the burn wound during healing process was usually incorporated of infiltration of inflammatory cells, granulation tissue formation and epithelialization within 7 - 12 days post-burn. Then, the surface of burn wound was partially ulcerated in association with epidermal necrosis, dermal disorganization and degeneration of the sebaceous gland 17 - 21 days post-burn. Finally, the regenerated skin retained the structure of normal skin at 28th day post-burn. Our study demonstrated that the histopathological changes of burn wounds involved deep dermis, and the pathological changes occurred at distinctive time phases were almost different in comparing to regular intact skin. Such age estimation of burn wounds is important when a cadaver or a burnt body has many burns of diverse times, especially in criminal cases.
 
</p></abstract><kwd-group><kwd>Forensic Medicine</kwd><kwd> Skin Pathology</kwd><kwd> Burn</kwd><kwd> Age of Wound</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>In forensic practice, it is doubtless that wound examination is one of the consequential and necessary areas for forensic pathologists. During the process of wound investigation, to assess the causalcorrelation between death and any wounds, forensic pathologists are always required to differentiate antemortem wounds from postmortem damage or to estimate wound age. It is likewise important to figure out whether a wound has vital reaction, and if so, how long before the wound has been sustained [<xref ref-type="bibr" rid="scirp.61999-ref1">1</xref>] . In other words, the determination of wound vitality or wound age has to be always performed. The short and simplified overview of wound healing can be adopted to determine wound vitality or wound age in forensic medicine. Forensic pathologists can determine how long a victim has been exposed by the age estimation of burns. However, aging of burn injuries by visual observation is sometimes difficult and uncertain [<xref ref-type="bibr" rid="scirp.61999-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.61999-ref3">3</xref>] .</p><p>Histopathological examination remains to be a more reliable technique, which provides an experimental basis for the distinction between ante- and post-mortem wounds, and determining the age of wounds [<xref ref-type="bibr" rid="scirp.61999-ref4">4</xref>] . Histo- pathological alterations characterizing the distinctive phases of wound healing can be applied to estimate the approximate age of wounds, especially of those inflicted within the early hours of wounding [<xref ref-type="bibr" rid="scirp.61999-ref5">5</xref>] . Therefore, aging of burn wounds is one of the most important medico-legal problems based on the observation of a normal course of the burn healing process. During the healing process, several morphologically distinguishable pheno- mena occur, and their microscopical detection determines the wound age whereas the absence of these para- meters provides fewer reliable results and often cannot be interpreted under forensic aspects [<xref ref-type="bibr" rid="scirp.61999-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.61999-ref4">4</xref>] . In this way, the following study aimed to recognizethe pathomorphological changes in healing of chronic deep second- degree burns that may be more constant in their time sequence, thus enabling an assessment of the burn wound vitality and age.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Animals</title><p>Thirty-six male Swiss albino mice of 10 - 12 weeks-old, 25 - 30 g body weight, were obtained from the Laboratory Animal House, High Institute of Public Health, Alexandria University, Alexandria, Egypt. The animals were randomized into control (unburnt) and burnt groups at one time. They were kept in cages numbered 1 to 6, and housed in a temperature-controlled room (27˚C - 30˚C). Twelve-hour light-dark cycle was maintained with lights on at 6 am and off at 6 pm. In order to minimize all undesired stressors, such as handling, habitat etc., the animals were acclimatized to the environment for at least one week in the animal house at the institutional department. The animals were allowed to recover, housed separately, and fed ad libitum until the wounds were harvested.</p></sec><sec id="s2_2"><title>2.2. Burn Injury Induction</title><p>Under ether anesthesia, animals were shaved and clipped on the dorsal area between the last thoracic and first sacrum vertebrae. The clipped areas were swabbed with betadine and ethanol 70%. Then, deep second-degree burn injuries were induced on the skin of the treated group by pressing a red-hot steel instrument 112˚C witha (1.5 &#215; 1.5 mm) cross sectional area for 2-second exposure time. The animal experiments were performed in accordance with the institutional and national guidelines for the care and use of laboratory animals.</p></sec><sec id="s2_3"><title>2.3. Histopathology</title><p>At zero day in control goup (unburnt group), and at 7th, 12th, 17th, 21st and 28th days after burning in burnt group, 6 animals were sacrificed by exsanguination under ether anesthesia. Then, burn wound samples were immediatly harvasted using a 6-mm punch biopsy. From each animal, one wound was immediately fixed in neutral buffered formalin 10% for a period of at least 24 hours. The fixed tissue specimens were then dehydrated in ethanol (50% - 100%) and embedded in paraffin, cut into sections of 4 - 5 &#181;m thickness parallel to the longi- tudinal axis of the body. The sections were stained using routine hematoxylin-eosin stain [<xref ref-type="bibr" rid="scirp.61999-ref6">6</xref>] . The phenotype of wound healing was assessed by light microscopy. From each sample, at least three sections through the center of the wound were examined for re-epithelialization, granulationt issue formation, and inflammatory response. The burnwound edge was used as the point where there was a clear margin in which subcutaneous fat tissue, mature collagen or hair follicles were absent.</p></sec></sec><sec id="s3"><title>3. Results</title><p>Under the light microscope, the normal intact skin reveals epidermis lined by stratified squamous epithelium with all layers; granular, basal, spinous and cornfied layers. The dermis is intact containing blood vessels and few lymphocytes (<xref ref-type="fig" rid="fig1">Figure 1</xref>). In relation to intact skin, all burn wounds were noted to involve deep dermis and the pathological changes of burn wounds at distinct time phases were almost different. On 7th day post-burn, the dermal and epidermal layers are disorganized with granulation tissue formation around sebaceous glands (<xref ref-type="fig" rid="fig2">Figure 2</xref>(a)). The superficial necrotic tissues in the dermis were liquefied, discharged and thinned. The epider- mis became necrotic due to collagen degeneration and granulation tissue formation. In addition, neoformative small-sized blood vessels with presence of fibroblast and infiltration of many inflammatory cells, including neutrophil, lymphocytes, polymorphs and histocytes were visible in wounds (<xref ref-type="fig" rid="fig2">Figure 2</xref>(b)). On 12th day post- burn, the wound character is still clearly similar to 7th day post-burn. However, the burn showing fibrinoid necrosis with degeneration of collagen and sebaceous gland (<xref ref-type="fig" rid="fig3">Figure 3</xref>(a) and <xref ref-type="fig" rid="fig3">Figure 3</xref>(b)).</p><p>On 17th day post-burn, the burn wound is showing partial surface ulceration with epidermal necrosis and loses. It was infiltrated with fibroblast, histocytes, lymphocytes and polymorphs (<xref ref-type="fig" rid="fig4">Figure 4</xref>(a)). The dermis shows disorganization with collagen and degeneration of the sebaceous gland (<xref ref-type="fig" rid="fig4">Figure 4</xref>(b)). On 21st day post- burn, the burn wound is showing partial surface ulceration with dermal granulation tissue formation (<xref ref-type="fig" rid="fig5">Figure 5</xref>). On 28th day post-burn, the epidermis becomes thin with dermal disorganization, fibrous tissue formation and degeneration of the hair follicle (<xref ref-type="fig" rid="fig6">Figure 6</xref>(a) and <xref ref-type="fig" rid="fig6">Figure 6</xref>(b)).</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Photomicrograph of skin of control animal (unburnt mice) stained with H &amp; E showing epidermis (E) lined by stratified squamous epithelium (Sq E) showing all layers (granular, basal, spinous and cornfied layers). The dermis (D) is intact containing blood vessels and few lymphocytes (&#215;400)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-2790092x6.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Photomicrograph of skin of burnt mice 7days post-burn stained with H &amp; E showing epidermal and dermal disorganization (E) with a granulation tissue (G) formation around sebaceous glands (S) ((a), &#215;400). The burn reveals collagen degeneration (C) and granulation tissue formation (G), formed of small-sized blood vessels (BV) with presence of fibroblast, lymphocytes (L), polymorphs (P) and histocytes ((b), &#215;400)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-2790092x7.png"/></fig><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Photomicrograph of skin of burnt mice 12 days post-burn stained with H &amp; E showing fibrinoid necrosis (F) and granulation tissue formation, formed of small-sized blood vessels with presence of fibroblast, polymorphs (P), histocytes (H) and lymphocytes ((a), &#215;400). The burn reveals collagen (C) and sebaceous gland degeneration(S) ((b), &#215;400)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-2790092x8.png"/></fig><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Photomicrograph of skin of burnt mice 17 days post-burn stained with H &amp; E showing surface ulceration (U) with granulation tissue formation (G) formed of fibroblast, histocytes (H), lymphocytes (L) and polymorphs (P) ((a), &#215;400). The burn reveals partial surface ulceration (U) with epidermal necrosis and loses. The dermis shows disorganization with collagen (C) and sebaceous gland (S) degeneration ((b), &#215;400)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-2790092x9.png"/></fig><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> Photomicrograph of skin of burnt mice 21 days post-burn stained with H &amp; E showing partial surface ulceration (U). Dermis shows granulation tissue formation (G) (&#215;400)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-2790092x10.png"/></fig><fig id="fig6"  position="float"><label><xref ref-type="fig" rid="fig6">Figure 6</xref></label><caption><title> Photomicrograph of skin of burnt mice 28 days post-burn stained with H &amp; E showing epidermal (E) thinning with dermal disorganization and fibrous tissue formation ((a), &#215;400). The burn reveals degeneration of the hair follicle (H) with fibrous (F) tissue formation (scar) ((b), &#215;400). (G), Granulation tissue formation; (P), Polymorphs</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-2790092x11.png"/></fig></sec><sec id="s4"><title>4. Discussion</title><p>From the viewpoint of forensic pathology as well, these pathomorphological changes show the possibility of available timing for wound age determination. Normal wound healing is usually divided into three stages: 1) inflammation, 2) epithelialization and granulation tissue formation, and 3) matrix formation and remodeling [<xref ref-type="bibr" rid="scirp.61999-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.61999-ref8">8</xref>] . Chronic wounds are characterized by a prolonged inflammatory response with disturbed cellular consti- tuents [<xref ref-type="bibr" rid="scirp.61999-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.61999-ref10">10</xref>] . Histologic examination of the burn edge, to include both the burned area and adjacent grossly unburned skin, may reveal vital reaction microscopically, consisting of acute inflammation, edema, and necrosis [<xref ref-type="bibr" rid="scirp.61999-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.61999-ref12">12</xref>] . These findings are present only in antemortem burns, thereby assisting in the delineation of whether the decedent was alive when the burns occurred. Additionally, a section of the skin in burns may document necrosis, vertical streaming of the epidermal nuclei, and homogenation of the dermal collagen. Our study demonstrated that the histopathological changes of burn wounds involved deep dermis and the pathological changes of burns at distinctive time phases were almost different in comparing to normal intact skin. On days 7 - 12 post-burn, the pathomorphological change was characterized by the disorganization with granulation tissue formation and necrosis of occurred in the burned epidermis and superficial dermis, revealing inflammatory response, with signs of “leukocyte infiltration”. The necrotic tissue began to liquefy and discharge increasingly as the disease course progressed [<xref ref-type="bibr" rid="scirp.61999-ref12">12</xref>] . Such changes increased around days 12 - 17 post-burn when dermal degeneration of sebaceous gland, fibroblasts, histocytes, as well as other repaired cells, showed signs of regene- ration.</p><p>On 7th day post-burn, wound liquefaction became noticeable and peaked. After that, liquefaction reduced with less necrotic tissue. The inflammatory response, however, remained correlated with the liquefaction of necrotic tissue. Repair by regeneration was noted on 12th day post-burn and manifested mainly by fibroblasts, histocytes, as well as other repaired cells. This stimulated the proliferation of peripheral fibroblasts and endothelia, and further formed granulation tissues, leading to final healing by epithelization [<xref ref-type="bibr" rid="scirp.61999-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.61999-ref12">12</xref>] . Later, the surface of burn wound is partially ulcerated with epidermal necrosis, dermal disorganization and degeneration of the sebaceous gland 17 - 21 days post-burn. After experiencing further differentiation and neoformation, the regenerated skin finally attained the structure of normal skin at 28th day post-burn. In this way, the study demonstrates that recognizing the histopathological changes in normal healing process of burns is more constant in their time sequence, thus enabling an assessment of the burn wound vitality and age. Such age estimation of burn wounds is vital when a cadaver or a burnt body has many burns of different ages, particularly in criminal cases.</p></sec><sec id="s5"><title>Cite this paper</title><p>Yasser S.El-Sayed, (2016) Time Course of Histomorphologic Features during Chronic Burn Wound Healing. Forensic Medicine and Anatomy Research,04,1-6. doi: 10.4236/fmar.2016.41001</p></sec></body><back><ref-list><title>References</title><ref id="scirp.61999-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Kondo, T. (2007) Timing of Skin Wounds. Legal Medicine (Tokyo), 9, 109-114. &lt;br /&gt; 
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