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        <title>Head &amp; Face Medicine - Latest Articles</title>
        <link>http://www.head-face-med.com</link>
        <description>The latest research articles published by Head &amp; Face Medicine</description>
        <dc:date>2010-08-20T00:00:00Z</dc:date>
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        <item rdf:about="http://www.head-face-med.com/content/6/1/21">
        <title>Gender specific quality of life in patients with oral squamous cell carcinomas</title>
        <description>Background:
The goal of this study was to evaluate the somatic and psychological effects by means of QUALITY OF LIFE (QOL) of surgical treatment of patients with oral squamous cell carcinoma. The factors gender, age, nicotine consumption, and tumour stage were taken into consideration.
Methods:
54 patients after surgical resection of oral squamous cell carcinomas (OSCC) were analysed from 01.09.2005 to 31.05.2008. Inclusion criteria for the study were: age at least 18 years, no indication or treatment of synchronous and metachronous tumours.German translations of the EORTC H&amp;N-35 and EORTC QLQ-C-30 questionnaires, as well as a general socioeconomic patient history were used as measuring instruments. The questionnaires were completed independently by the patients. The answers were translated into scale values for statistical evaluation using appropriate algorithms.
Results:
Analysis of the EORTC-QLQ-C-30 questionnaires demonstrated a tendency of more negative assessment of emotional function among the female participants, and a more negative evaluation of social function among the male participants. Greater tumour sizes showed significantly lower bodily function (p = 0.018). While a smaller tumour size was significantly associated with lower cognitive functioning (p = 0.031). Other cofactors such as age, nicotine consumption, and tumour stage only showed a tendency to influence the quality of sleep and daily life.
Conclusions:
The data obtained within this investigation demonstrated that gender had the most significant power on the subjectively perceived postoperative quality of life. This factor is important e.g. in preoperative decision making regarding immediate microvascular reconstruction after e.g. mandibular resection and therefore QOL assessment should become integral component of the care of patients with OSCC.</description>
        <link>http://www.head-face-med.com/content/6/1/21</link>
                <dc:creator>Oliver Maciejewski</dc:creator>
                <dc:creator>Ralf Smeets</dc:creator>
                <dc:creator>Frank Gerhards</dc:creator>
                <dc:creator>Andreas Kolk</dc:creator>
                <dc:creator>Frank Kloss</dc:creator>
                <dc:creator>Jamal Stein</dc:creator>
                <dc:creator>Adrian Kasaj</dc:creator>
                <dc:creator>Felix Koch</dc:creator>
                <dc:creator>Maurice Grosjean</dc:creator>
                <dc:creator>Dieter Riediger</dc:creator>
                <dc:creator>Sareh Said Yekta</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:21</dc:source>
        <dc:date>2010-08-20T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-21</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>21</prism:startingPage>
        <prism:publicationDate>2010-08-20T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.head-face-med.com/content/6/1/20">
        <title>Central odontogenic fibroma: a case report with long-term follow-up</title>
        <description>An osteolytic tumour of the mandible with prominent expansive growth on the alveolar ridge and displacement of the involved teeth is described in a 28-year-old man. The lesion was diagnosed as a central odontogenic fibroma, an uncommon benign neoplasm derived from dental apparatus, and was removed by curettage. The patient remains asymptomatic after thirteen years of follow-up, which supports the claimed indolent behavior of this poorly documented disease and the adequacy of a conservative surgical treatment.</description>
        <link>http://www.head-face-med.com/content/6/1/20</link>
                <dc:creator>Marco Brazao-Silva</dc:creator>
                <dc:creator>Alexandre Fernandes</dc:creator>
                <dc:creator>Antonio Durighetto-Junior</dc:creator>
                <dc:creator>Sergio Cardoso</dc:creator>
                <dc:creator>Adriano Loyola</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:20</dc:source>
        <dc:date>2010-08-13T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-20</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>20</prism:startingPage>
        <prism:publicationDate>2010-08-13T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.head-face-med.com/content/6/1/19">
        <title>Surgical treatment of gingival overgrowth with 10 years follow up</title>
        <description>Background:
In some pathological conditions, gingivitis caused by plaque accumulation can be more severe, with the result of an overgrowth. Nevertheless, the overgrowth involves the gingival margin with extension to the inter-dental papilla. The lesion may involve the inter-proximal spaces, and become so extensive that the teeth are displaced and their crowns covered. Severe overgrowth may lead to impairment in aesthetic and masticatory functions, requiring surgical excision of the excessive tissue. Aim of this study is to describe an operative protocol for the surgical treatment of localized gingival overgrowth analyzing the surgical technique, times and follow-up.
Methods:
A total of 20 patients were enrolled and underwent initial, non surgical, periodontal treatment and training sessions on home oral hygiene training. The treatment plan involved radical exeresis of the mass followed by positioning of an autograft of connective tissue and keratinized gingiva.
Results:
During 10 years of follow-up, all the grafts appeared well vascularized, aesthetically satisfactory, and without relapse.
Conclusions:
Periodontal examinations, surgical procedures, and dental hygiene with follow-up are an essential part of the treatment protocol. However, additional effort is needed from the patient. Hopefully, the final treatment result makes it all worthwhile.</description>
        <link>http://www.head-face-med.com/content/6/1/19</link>
                <dc:creator>Andrea Ballini</dc:creator>
                <dc:creator>Adele Scattarella</dc:creator>
                <dc:creator>Vito Crincoli</dc:creator>
                <dc:creator>Roberto Carlaio</dc:creator>
                <dc:creator>Francesco Papa</dc:creator>
                <dc:creator>Letizia Perillo</dc:creator>
                <dc:creator>Teodoro Romanazzo</dc:creator>
                <dc:creator>Maria Bux</dc:creator>
                <dc:creator>Gianna Nardi</dc:creator>
                <dc:creator>Angela Dituri</dc:creator>
                <dc:creator>Stefania Cantore</dc:creator>
                <dc:creator>Francesco Pettini</dc:creator>
                <dc:creator>Felice Grassi</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:19</dc:source>
        <dc:date>2010-08-12T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-19</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>19</prism:startingPage>
        <prism:publicationDate>2010-08-12T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.head-face-med.com/content/6/1/18">
        <title>3D digital stereophotogrammetry: A practical guide to facial image acquisition</title>
        <description>The use of 3D surface imaging technology is becoming increasingly common in craniofacial clinics and research centers. Due to fast capture speeds and ease of use, 3D digital stereophotogrammetry is quickly becoming the preferred facial surface imaging modality. These systems can serve as an unparalleled tool for craniofacial surgeons, proving an objective digital archive of the patient&apos;s face without exposure to radiation. Acquiring consistent high-quality 3D facial captures requires planning and knowledge of the limitations of these devices. Currently, there are few resources available to help new users of this technology with the challenges they will inevitably confront. To address this deficit, this report will highlight a number of common issues that can interfere with the 3D capture process and offer practical solutions to optimize image quality.</description>
        <link>http://www.head-face-med.com/content/6/1/18</link>
                <dc:creator>Carrie Heike</dc:creator>
                <dc:creator>Kristen Upson</dc:creator>
                <dc:creator>Erik Stuhaug</dc:creator>
                <dc:creator>Seth Weinberg</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:18</dc:source>
        <dc:date>2010-07-28T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-18</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>18</prism:startingPage>
        <prism:publicationDate>2010-07-28T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.head-face-med.com/content/6/1/17">
        <title>Release kinetics of VEGF165 from a collagen matrix and structural matrix changes in a circulation model</title>
        <description>Background:
Current approaches in bone regeneration combine osteoconductive scaffolds with bioactive cytokines like BMP or VEGF. The idea of our in-vitro trial was to apply VEGF165 in gradient concentrations to an equine collagen carrier and to study pharmacological and morphological characteristics of the complex in a circulation model.
Methods:
Release kinetics of VEGF165 complexed in different quantities in a collagen matrix were determined in a circulation model by quantifying protein concentration with ELISA over a period of 5 days. The structural changes of the collagen matrix were assessed with light microscopy, native scanning electron microscopy (SEM) as well as with immuno-gold-labelling technique in scanning and transmission electron microscopy (TEM).
Results:
We established a biological half-life for VEGF165 of 90 minutes. In a half-logarithmic presentation the VEGF165 release showed a linear declining gradient; the release kinetics were not depending on VEGF165 concentrations. After 12 hours VEGF release reached a plateau, after 48 hours VEGF165 was no longer detectable in the complexes charged with lower doses, but still measurable in the 80 &#956;g sample. At the beginning of the study a smear layer was visible on the surface of the complex. After the wash out of the protein in the first days the natural structure of the collagen appeared and did not change over the test period.
Conclusions:
By defining the pharmacological and morphological profile of a cytokine collagen complex in a circulation model our data paves the way for further in-vivo studies where additional biological side effects will have to be considered. VEGF165 linked to collagen fibrils shows its improved stability in direct electron microscopic imaging as well as in prolonged release from the matrix. Our in-vitro trial substantiates the position of cytokine collagen complexes as innovative and effective treatment tools in regenerative medicine and and may initiate further clinical research.</description>
        <link>http://www.head-face-med.com/content/6/1/17</link>
                <dc:creator>Johannes Kleinheinz</dc:creator>
                <dc:creator>Susanne Jung</dc:creator>
                <dc:creator>Kai Wermker</dc:creator>
                <dc:creator>Carsten Fischer</dc:creator>
                <dc:creator>Ulrich Joos</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:17</dc:source>
        <dc:date>2010-07-19T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-17</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>17</prism:startingPage>
        <prism:publicationDate>2010-07-19T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.head-face-med.com/content/6/1/16">
        <title>Reconstruction of a maxillary defect with a fibula graft and titanium mesh using CAD/CAM techniques: Case report</title>
        <description>We present a case of maxillary and orbital floor reconstruction with a microvascular fibula graft and an individualized titanium mesh. Both were planned virtually; templates were made by rapid prototyping. The postoperative computertomography scans showed that the planned positions were achieved correctly. This case report illustrates maxillary reconstruction performed with a special template technique and demonstrates the possibilities of computer aided design/computer aided manufacturing (CAD/CAM) applications in reconstructive surgery.</description>
        <link>http://www.head-face-med.com/content/6/1/16</link>
                <dc:creator>Bernd Lethaus</dc:creator>
                <dc:creator>Peter Kessler</dc:creator>
                <dc:creator>Roland Bockmann</dc:creator>
                <dc:creator>Lucas Poort</dc:creator>
                <dc:creator>Rene Tolba</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:16</dc:source>
        <dc:date>2010-07-19T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-16</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>16</prism:startingPage>
        <prism:publicationDate>2010-07-19T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.head-face-med.com/content/6/1/15">
        <title>Human papillomavirus-mediated carcinogenesis and HPV-associated oral and oropharyngeal squamous cell carcinoma. 
Part II: Human papillomavirus associated oral and oropharyngeal squamous cell carcinoma
</title>
        <description>Human papillomavirus (HPV) infection of the mouth and oropharynx can be acquired by a variety of sexual and social forms of transmission. HPV-16 genotype is present in many oral and oropharyngeal squamous cell carcinomata. It has an essential aetiologic role in the development of oropharyngeal squamous cell carcinoma in a subset of subjects who are typically younger, are more engaged with high-risk sexual behaviour, have higher HPV-16 serum antibody titer, use less tobacco and have better survival rates than in subjects with HPV-cytonegative oropharyngeal squamous cell carcinoma. In this subset of subjects the HPV-cytopositive carcinomatous cells have a distinct molecular profile.In contrast to HPV-cytopositive oropharyngeal squamous cell carcinoma, the causal association between HPV-16 and other high-risk HPV genotypes and squamous cell carcinoma of the oral mucosa is weak, and the nature of the association is unclear.It is likely that routine administration of HPV vaccination against high-risk HPV genotypes before the start of sexual activity will bring about a reduction in the incidence of HPV-mediated oral and oropharyngeal squamous cell carcinoma.This article focuses on aspects of HPV infection of the mouth and the oropharynx with emphasis on the link between HPV and squamous cell carcinoma, and on the limitations of the available diagnostic tests in identifying a cause-and-effect relationship of HPV with squamous cell carcinoma of the mouth and oropharynx.</description>
        <link>http://www.head-face-med.com/content/6/1/15</link>
                <dc:creator>Liviu Feller</dc:creator>
                <dc:creator>Neil Wood</dc:creator>
                <dc:creator>Razia Khammissa</dc:creator>
                <dc:creator>Johan Lemmer</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:15</dc:source>
        <dc:date>2010-07-15T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-15</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>15</prism:startingPage>
        <prism:publicationDate>2010-07-15T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.head-face-med.com/content/6/1/14">
        <title>Human papillomavirus-mediated carcinogenesis and HPV-associated oral and oropharyngeal squamous cell carcinoma.
Part 1: Human papillomavirus-mediated carcinogenesis
</title>
        <description>High-risk human papillomavirus (HPV) E6 and E7 oncoproteins are essential factors for HPV-induced carcinogenesis, and for the maintenance of the consequent neoplastic growth. Cellular transformation is achieved by complex interaction of these oncogenes with several cellular factors of cell cycle regulation including p53, Rb, cyclin-CDK complexes, p21 and p27. Both persistent infection with high-risk HPV genotypes and immune dysregulation are associated with increased risk of HPV-induced squamous cell carcinoma.</description>
        <link>http://www.head-face-med.com/content/6/1/14</link>
                <dc:creator>Liviu Feller</dc:creator>
                <dc:creator>Neil Wood</dc:creator>
                <dc:creator>Razia Khammissa</dc:creator>
                <dc:creator>Johan Lemmer</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:14</dc:source>
        <dc:date>2010-07-15T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-14</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>14</prism:startingPage>
        <prism:publicationDate>2010-07-15T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.head-face-med.com/content/6/1/13">
        <title>A hypothetical correlation between hyaluronic acid gel and development of cutaneous metaplastic synovial cyst
</title>
        <description>Thousands of patients receive hyaluronic acid filler injections, and the effects are generally considered acceptable. The acid rarely causes cutaneous reactions, which are only occasionally reported in the literature.The aim of the present work is to analyze a clinical case that has never been reported in the literature to our knowledge. This case is of a 26-year-old woman who presented with a cyst in the infrazygomatic region that was injected with non-animal stabilized hyaluronic acid at another centre a few months ago.Consequently, we made an external incision to remove the neoplasm: histological examination of the capsule revealed it to be a cutaneous metaplastic synovial cyst.</description>
        <link>http://www.head-face-med.com/content/6/1/13</link>
                <dc:creator>Francesco Inchingolo</dc:creator>
                <dc:creator>Marco Tatullo</dc:creator>
                <dc:creator>Fabio Abenavoli</dc:creator>
                <dc:creator>Massimo Marrelli</dc:creator>
                <dc:creator>Alessio Inchingolo</dc:creator>
                <dc:creator>Andrea Servili</dc:creator>
                <dc:creator>Angelo Inchingolo</dc:creator>
                <dc:creator>Gianna Dipalma</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:13</dc:source>
        <dc:date>2010-07-15T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-13</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>13</prism:startingPage>
        <prism:publicationDate>2010-07-15T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.head-face-med.com/content/6/1/12">
        <title>The impact of bisphosphonates on the osteoblast proliferation and Collagen gene expression in vitro</title>
        <description>Background:
Bisphosphonates are widely used in the clinical treatment of bone diseases with increased bone resorption. In terms of side effects, they are known to be associated with osteonecrosis of the jaw (BONJ).The objective of this study was to evaluate the effect of bisphosphonates on osteoblast proliferation by cell count and gene expression analysis of cyclin D1 in vitro. Furthermore, the gene expression of the extracellular matrix protein collagen type I was evaluated. Nitrogen-containing and non-nitrogen-containing bisphosphonates have been compared on gene expression levels.
Methods:
Human osteoblast obtained from hip bone were stimulated with zoledronate, ibandronate and clodronate at concentrations of 5 &#215; 10-5M over the experimental periods of 1, 2, 5, 10 and 14 days. At each point in time, the cells were dissolved, the mRNA extracted, and the gene expression level of cyclin D1 and collagen type I were quantified by Real-Time RT-PCR. The gene expression was compared to an unstimulated osteoblast cell culture for control.
Results:
The proliferation appeared to have been influenced only to a small degree by bisphosphonates. Zolendronate led to a lower cyclin D1 gene expression after 10 days. The collagen gene expression was enhanced by nitrogen containing bisphosphonates, decreased however after day 10. The non-nitrogen-containing bisphosphonate clodronate, however, did not significantly influence cyclin D1 and collagen gene expression.
Conclusions:
The above data suggest a limited influence of bisphosphonates on osteoblast proliferation, except for zoledronate. The extracellular matrix production seems to be initially advanced and inhibited after 10 days. Interestingly, clodronate has little influence on osteoblast proliferation and extracellular matrix production in terms of cyclin D1 and collagen gene expression.</description>
        <link>http://www.head-face-med.com/content/6/1/12</link>
                <dc:creator>Felix Koch</dc:creator>
                <dc:creator>Sareh Said Yekta</dc:creator>
                <dc:creator>Christina Merkel</dc:creator>
                <dc:creator>Thomas Ziebart</dc:creator>
                <dc:creator>Ralf Smeets</dc:creator>
                <dc:source>Head &amp; Face Medicine 2010, 6:12</dc:source>
        <dc:date>2010-07-09T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1746-160X-6-12</dc:identifier>
        <prism:publicationName>Head &amp; Face Medicine</prism:publicationName>
        <prism:issn>1746-160X</prism:issn>
        <prism:volume>6</prism:volume>
        <prism:startingPage>12</prism:startingPage>
        <prism:publicationDate>2010-07-09T00:00:00Z</prism:publicationDate>
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