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Case Reports in Dentistry
Volume 2013 (2013), Article ID 262410, 8 pages
The Correlation between Chronic Periodontitis and Oral Cancer
1Department of Oral and Maxillofacial Surgery-Plastic Surgery, Johannes Gutenberg University of Mainz, Medical Center, Augustusplatz 2, 55131 Mainz, Germany
2Institute of Pathology, University of Mainz, Medical Surgery, Langenbeckstraße 1, 55131 Mainz, Germany
3Department of Operative Dentistry and Periodontology, Johannes Gutenberg-University, Augustusplatz 2, 55131 Mainz, Germany
Received 16 May 2013; Accepted 9 June 2013
Academic Editors: D. W. Boston, A. C. B. Delbem, and A. Milosevic
Copyright © 2013 Maximilian Krüger et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Infections are increasingly considered as potential trigger for carcinogenesis apart from risk factors like alcohol and tobacco. The discussion about human papilloma virus (HPV) in oral squamous cell carcinoma (OSCC) points at a general role of infection for the development of oral carcinomas. Furthermore, first studies describe a correlation between chronic periodontitis and OSCC, thus, characterizing chronic inflammation as being a possible trigger for OSCC. In front of this background, we present four well-documented clinical cases. All patients showed a significant anatomical relation between OSCC and clinical signs of chronic periodontitis. The interindividual differences of the clinical findings lead to different theoretical concepts: two with coincidental appearance of OSCC and chronic periodontitis and two with possible de novo development of OSCC triggered by chronic inflammation. We conclude that the activation of different inflammatory cascades by chronic periodontitis negatively affects mucosa and bone. Furthermore, the inflammatory response has the potential to activate carcinogenesis. Apart from a mere coincidental occurrence, two out of four patients give first clinical hints for a model wherein chronic periodontitis represents a potential risk factor for the development of OSCC.
Squamous cell carcinoma is the most frequent malignancy in the oral cavity and with nearly 400.000 new diagnosed patients worldwide each year; it represents the sixth frequent malignant tumor. Despite multimodality approaches for the treatment comprising surgery and adjuvant chemo- and radiation therapy, the disease still has a low overall survival rate of about 50% [1, 2]. The development of new therapeutic strategies with improved treatment options or possible prevention of oral squamous cell carcinoma (OSCC) requests a substantial understanding of its etiology. The last years have revealed more detailed information about different risk factors for the development of OSCC. Important risk factors of the general accepted multistep carcinogenesis model are genetic predisposition , presence of premalignant lesions , and environmental or behavioural carcinogenic triggers, for example, the ingestion of tobacco and alcohol . Recently, the influence of infection and inflammation for cancer development has been discussed. Associations between human papilloma virus (HPV) infection and oropharyngeal carcinomas have been documented . These patients are typically Caucasians, nonsmokers, nondrinkers, and one decade younger on average than people suffering from HPV negative carcinomas. Intriguingly, patients with HPV-positive oropharyngeal carcinomas had a significant better prognosis than the HPV negative collective [7, 8]. This finding might point at subtypes of infection-induced carcinomas with different clinical behaviours, thus, stressing the need of further characterization. Comparably, the predominant infection within the oral cavity is chronic periodontitis, and its role for the development of oral cancer was likewise recently discussed [9, 10]. Herein, periodontitis occurs as chronic inflammatory process characterized by specific bacteria and the loss of attached gingiva and alveolar bone, with consecutive development of periodontal pockets and loss of teeth . A recently published work by Tezal et al. found the loss of bone as clinical sign for chronic periodontitis being an independent risk factor for the development of carcinoma within the oral cavity . In front of this background, the case series at hand comprises four patients treated at our clinical Department for OSCC. Within these, the synopsis of clinical appearance, radiologic findings, and cross-sectional resection specimen offer an association of the carcinoma to the periodontal space with signs of chronic inflammation. The different clinical aspects are discussed comprising the available literature on this topic.
2. Case Presentations
Case 1. A 59-year-old woman presented herself with an exophytic mass of 2 cm adherent to the mandible and localized distally of tooth 36. The tooth revealed signs of chronic periodontitis with bleeding on probing, attachment loss and a 5 mm deep pocket, and significant mobility on clinical examination. Polymerase chain reaction (Micro-ident, Hain Lifescience GmbH D-72147 Nehren) (PCR) revealed an infection with Porphyromonas gingivalis and Tannerella forsythia (red complex). The expansion of the tumor reached from the sulcus glossoalveolaris with its center along the alveolar crest to the adjacent buccal mucosa (Figure 1). The patient reported herself to be a never smoker and never ingested alcohol. Oral hygiene habits were sufficient. No other precursor lesions like leukoplakia, erythroplakia, or signs of oral lichen planus were found on examination. The visit of our department was induced by progressive pain and increasing swelling. The preoperatively taken orthopantomography (OPTG) revealed a considerable generalized horizontal type of bone loss within the upper and the lower jaw, as also a distinct inter- and periradicular osteolytic lesion at the region of 36 (Figure 2). A both-sided selective neck dissection  and partial resection of the mandible followed. The clinical appearance (Figure 1) showed an exophytic mass with contact to the distal root of 36. Intriguingly, the OPTG showed no arrosion of the distal mandible but apparently an inhomogeneous radiolucency between the roots of the molar. The cross-section specimen (Figure 3) furthermore highlights the interradicular spreading of the tumor without an infiltration of cancellous bone or the distal alveolar crest. HPV status by p16 immunostaining was negative.
Taking all clinical findings together, the present case supports the hypothesis of a possible de novo development of malignancy from the interradicular periodontium.
Case 2. A 48-year-old man presented himself with a histological verified squamous cell carcinoma of the left mandible adjacent to the partially retained tooth 37 surrounded by a bony defect of 3 mm. Analysis of the bacteria (Micro-ident, Hain Lifescience GmbH D-72147 Nehren) inside the pocket showed an infection with Peptostreptococcus micros and Fusobacterium nucleatum (orange complex) as well as Eikenella corrodens and Capnocytophaga sp. (green complex). The patient reported recurring inflammation in the left lower quadrant for a period of six weeks. Prior to the planned osteotomy of the wisdom tooth, the dentist had taken a scalpel biopsy, giving evidence for OSCC. Clinical examination revealed an ulcerous lesion with dominant signs of perifocal inflammation. The ulcer was delineated by a rigid wall of mucosa attached to the alveolar crest related to 37 and 38 (Figure 4). The patient declared to be a nonsmoker but admitted occasional alcohol consumption. Oral hygiene was assessed to be average, and no other precursor lesions were present. The preoperatively taken OPTG (Figure 5) revealed considerable periradicular bone loss in regions 37 and 36 analogous to typical radiologic findings in patients with moderate to advanced chronic periodontitis. The patient underwent radical intended resection of the tumor. Figure 6 shows the resection specimen from a distal view. The tumor is mainly localized in the interdental space of 37 and 36 with distinct relation to the periodontal space of the crown 36. The beginning infiltration of the mouth floor becomes apparent. Figure 7 shows the microscopic view with arrosion of the bone by the tumor cells. HPV status by p16 immunostaining was negative.
Case 3. A 50-year-old man was referred to our clinic by a maxillofacial surgeon with diagnosis of a squamous cell carcinoma of the right mandible. The clinical examination revealed a tumor of 4 cm in diameter, localized at the alveolar crest distal of 46 with extensions to the adjacent floor of the mouth. Around the ulcer, fields of homogeneous leukoplakia were detectable (Figure 8). The patient suffered from generalized advanced chronic periodontitis, exhibiting pocket depths up to 7 mm with bleeding on probing. Analysis of bacteria (Micro-ident, Hain Lifescience GmbH D-72147 Nehren) revealed infection with Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola (red complex), Peptostreptococcus micros, Fusobacterium nucleatum (orange complex), and Campylobacter rectus (orange-associated complex). Oral hygiene was extremely poor with high amounts of soft and hard debris on the furthermore carious teeth. The patient reported to be a heavy smoker (60 pack years) and drinker (>3 L beer a day). The OPTG (Figure 9) exhibited severe general bone loss with a basin-like translucency comprising the last distal molars of the right mandible. A radical intended operation followed. Figure 10 shows a transverse section of the resected mandible from a lingual view. Herein, the tumor surrounds the empty alveoli of the artificially removed right molars with considerable infiltration of the alveolar bone. HPV status by p16 immunostaining was negative.
Case 4. A 53-year-old man was admitted to our clinic with the histological verified diagnosis of a squamous cell carcinoma of the anterior floor of the mouth. The patient noticed an indolent growing mass five weeks before admission. Figure 11 gives a picture of the clinical situation. Beside a space consuming sublingual mass with deviation of the lingual frenulum, a small erosive lesion lingual from the left lower anterior teeth (region: teeth 31 to 34) with subtle perifocal leukoplakia around the center of the lesion is shown. The examination revealed a solid tumor formation with its center mainly on the left floor of mouth. The tumor expanded from the left angle of the mandible with a midline crossing to the region of the first right lower incisor. Adherence to the bone was detectable in the region of the left lower canine and the first premolar. The oral hygiene status was moderate. Investigation of periodontal pockets revealed depths up to 4 mm and bleeding on probing. The patient smoked 10 cigarettes per day for ten years and occasionally drank a glass of wine. The OPTG (Figure 12) revealed a generalized horizontal type of bone loss within both jaws, with additional vertical bony defects and translucency as radiologic finding for an erosive process in the left anterior lower jaw. The radical intended surgery consisted of a bloc resection including parts of the mandible, tongue, floor of mouth, and hyoid with complete bilateral selective functional neck dissection . The split-resection specimen (Figure 13) shows a periradicular tumor formation along the root of the canine with infiltration of the neighboring cancellous bone. HPV status by p16 immunostaining was positive, as shown in Figure 14.
A brief summary of all cases is given in Table 1.
Our study presents four thoroughly documented cases with alveolar squamous cell carcinomas being directly associated to teeth that show considerable signs of chronic periodontitis. Chronic periodontitis represents the most common infection worldwide with high clinical relevance for the dentist. In front of this clinical setting, four different models of chronic periodontitis with alveolar squamous cell carcinomas are discussed as follows. The first patient had no precursor lesions, and no other risk factors had been identified except clinical signs of chronic periodontitis. In this patient, a de novo development caused by genomic instability as consequence of chronic inflammation caused by gram-negative bacteria as postulated by Guerra et al. appears possible . In this model, chronic periodontitis itself would trigger the development of oral squamous cell carcinoma. Recently, there is improving interest in the development of various types of cancer and their association to inflammation as also the underlying pathophysiological mechanisms that lead to malignant transformation . One important factor in cancer-related inflammation is the transcription factor NF-B. Beside its function as key coordinator of innate inflammation and immunity by activated expression of inflammatory cytokines, adhesion molecules, and angiogenic factors, it has also been identified as endogenous tumour promoter . Moreover, it is substantially involved in the inflammatory process of chronic periodontitis . In addition, an association between oral cancer and chronic mechanical trauma was also described , suggesting that inflammation independent of its cause may predispose to cancer. Hereby, malignant transformation of oral epithelium would be a consequence of the immune response like macrophage and T-cell activation and cytokine release (e.g., IL-1, IL-8, and TNF-α) . Aside malignant transformation as sequel of unspecific inflammation, a specific bacterial, or viral agent may also promote malignancies. This sequence is supposed for gastric lymphomas , H. pylori infection and gastric cancer , Hepatitis B Virus (HBV) and HCV infection in liver cancer  and HPV 16/18 infection in head and neck  or cervical cancer . Herein, microbial activation of inflammatory cells leads to a respiratory burst and release of free radicals, which can contribute transformation to malignancy by DNA damage, peroxidation of lipids, or disturbance of physiological posttranslational modification of proteins . Taken together, either genomic instability directly induced by the bacterial agent itself or as consequence of immunological response to chronic inflammation, both are main characteristics of chronic periodontitis. The clinical relevance of chronic periodontitis for the development of OSCC was investigated by Tezal et al. In a case control model, the loss of bone as clinical sign for chronic periodontitis was an independent risk factor for tongue carcinomas and was still of significance in a multiple regression model . Particularly, these patients would benefit from periodontal therapy in terms of primary prevention. The second case offers another possible scenario. Here, chronic periodontitis acts as promoter for the invasion of tumor cells into the bone. During the course of chronic periodontitis, the loss of clinical attachment level and the underlying bone is substantially triggered. The periodontal-localized inflammation macerates the cancellous bone by enhanced osteoclastic activity which may constitute a potential route for invasion of an adjacent carcinoma. Osteoclastic activity is enhanced by proinflammatory molecules like IL-1 or LPS , which can be found in gingival crevicular fluid (GCF) during chronic periodontitis . Furthermore, seven potential routes for invasion of the mandible by OSCC have been reviewed by Brown . Beside the occlusal route, neural foramina, attached gingiva, cortical bone defects in the edentulous ridge, or infiltration by secondary tumors in the neck through the lower border, the periodontal membrane in the dentate mandible was hypothesized as a possible way for tumor invasion by Bhattathiri and Nair in 1991 . Supposing the periodontal space a weak point for tumor invasion, the instance of periodontal inflammation may promote an invasion of the mandible by a neighbored tumor [15, 19]. The cross- sectional specimen of the second case underlines this possible scenario with a tumor infiltrating the periodontal space, the surrounding adjacent cancellous bone, and the neighbored floor of the mouth.
The third case is an example for chronic periodontitis being a well-known comorbidity in oral cancer patients. The patient was a heavy smoker and drinker with insufficient oral hygiene. All these habits are for themselves potential risk factors for the development of oral cancer and chronic periodontitis [5, 30–32]. In this patient, chronic periodontitis and OSCC seem to be a coincidence without an option to uncover cause and effect.
An accredited model for the development of OSCC is the multistep theory . Herein, the oral mucosa undergoes different developmental stages from hyperkeratosis over different degrees of dysplasia to invasive cancer, while each level shows consecutive accompanying alterations within the genetic profile . Accordingly, it appears possible, that chronic periodontitis may trigger the pathogenesis of precancerous lesions. In case four, the clinical inspection of the oral cavity revealed a vast field of leukoplakia at the anterior floor of mouth. Besides, the clinical manifest OSCC and multiple teeth were affected by chronic periodontitis. A cross-interaction between the special inflammatory milieu with enhanced levels of proinflammatory cytokines and a change in the bacterial environment may induce the development and progression of precancerous lesions in the alveolar mucosa. This thesis was reinforced recently by Meisel et al., who identified chronic periodontitis as a risk factor for the development of leukoplakia predisposing for oral cancer .
We presented four clinical scenarios of OSCC in the neighbourhood of teeth affected by chronic periodontitis for discussion of the clinical relevance. Clinical experience characterizes most OSCC as coincidence since chronic periodontitis and the oral malignancy share multiple risk factors impeding a definition of cause and effect. On the other hand, we found clinical hints for an interaction of OSCC and chronic periodontitis by means of invasion route preformation or a promotive effect on present precursor lesions. Finally, we give an example for a possible de novo synthesis of the OSCC in a patient without other risk factors. These patients, in particular, would greatly benefit from early therapy of the underlying chronic periodontitis in terms of a primary prevention.
Conflict of Interests
The authors declare that they have no conflict of interests. There are no financial or personal relationships with other people or organisations inappropriately influencing our work. Furthermore, the authors state that there were no sources of funding.
- S. H. Landis, T. Murray, S. Bolden, and P. A. Wingo, “Cancer Statistics, 1999,” CA: A Cancer Journal for Clinicians, vol. 49, no. 1, pp. 8–31, 1999.
- D. M. Parkin, F. Bray, J. Ferlay, and P. Pisani, “Global cancer statistics, 2002,” CA: A Cancer Journal for Clinicians, vol. 55, no. 2, pp. 74–108, 2005.
- P. Rusin, L. Markiewicz, and I. Majsterek, “Genetic predeterminations of head and neck cancer,” Postępy Higieny i Medycyny Doświadczalnej, vol. 62, pp. 490–501, 2008.
- P.-O. Rödström, M. Jontell, U. Mattsson, and E. Holmberg, “Cancer and oral lichen planus in a Swedish population,” Oral Oncology, vol. 40, no. 2, pp. 131–138, 2004.
- C. Pelucchi, S. Gallus, W. Garavello, C. Bosetti, and C. L. Vecchia, “Alcohol and tobacco use, and cancer risk for upper aerodigestive tract and liver,” European Journal of Cancer Prevention, vol. 17, no. 4, pp. 340–344, 2008.
- M. Tezal, M. S. Nasca, D. L. Stoler et al., “Chronic periodontitis-human papillomavirus synergy in base of tongue cancers,” Archives of Otolaryngology, vol. 135, no. 4, pp. 391–396, 2009.
- C. Fakhry, W. H. Westra, S. Li et al., “Improved survival of patients with human papillomavirus—positive head and neck squamous cell carcinoma in a prospective clinical trial,” Journal of the National Cancer Institute, vol. 100, no. 4, pp. 261–269, 2008.
- S. Marur, G. D'Souza, W. H. Westra, and A. A. Forastiere, “HPV-associated head and neck cancer: a virus-related cancer epidemic,” The Lancet Oncology, vol. 11, no. 8, pp. 781–789, 2010.
- M. S. Meyer, K. Joshipura, E. Giovannucci, and D. S. Michaud, “A review of the relationship between tooth loss, periodontal disease, and cancer,” Cancer Causes and Control, vol. 19, no. 9, pp. 895–907, 2008.
- D. S. Michaud, K. Joshipura, E. Giovannucci, and C. S. Fuchs, “A prospective study of periodontal disease and pancreatic cancer in US male health professionals,” Journal of the National Cancer Institute, vol. 99, no. 2, pp. 171–175, 2007.
- B. Burt and Research, Science and Therapy Committee of the American Academy of Periodontology., “Position paper: epidemiology of periodontal diseases,” Journal of Periodontology, vol. 76, no. 8, pp. 1406–1419, 2005.
- M. Tezal, M. A. Sullivan, A. Hyland et al., “Chronic periodontitis and the incidence of head and neck squamous cell carcinoma,” Cancer Epidemiology Biomarkers and Prevention, vol. 18, no. 9, pp. 2406–2412, 2009.
- K. T. Robbins, G. Clayman, P. A. Levine et al., “Neck dissection classification update: revisions proposed by the American Head and Neck Society and the American Academy of Otolaryngology-Head and Neck Surgery,” Archives of Otolaryngology, vol. 128, no. 7, pp. 751–758, 2002.
- L. Guerra, R. Guidi, and T. Frisan, “Do bacterial genotoxins contribute to chronic inflammation, genomic instability and tumor progression?” FEBS Journal, vol. 278, no. 23, pp. 4577–4588, 2011.
- S. F. Moss and M. J. Blaser, “Mechanisms of disease: inflammation and the origins of cancer,” Nature Clinical Practice Oncology, vol. 2, no. 2, pp. 90–97, 2005.
- M. Karin, “Nuclear factor-κB in cancer development and progression,” Nature, vol. 441, no. 7092, pp. 431–436, 2006.
- Y. Nagahama, T. Obama, M. Usui et al., “Oxidized low-density lipoprotein-induced periodontal inflammation is associated with the up-regulation of cyclooxygenase-2 and microsomal prostaglandin synthase 1 in human gingival epithelial cells,” Biochemical and Biophysical Research Communications, vol. 413, no. 4, pp. 566–571, 2011.
- E. D. Piemonte, J. P. Lazos, and M. Brunotto, “Relationship between chronic trauma of the oral mucosa, oral potentially malignant disorders and oral cancer,” Journal of Oral Pathology and Medicine, vol. 39, no. 7, pp. 513–517, 2010.
- A. Mantovani, P. Allavena, A. Sica, and F. Balkwill, “Cancer-related inflammation,” Nature, vol. 454, no. 7203, pp. 436–444, 2008.
- M. Lecuit, M. C. Peterson, F. Suarez, and O. Lortholary, “Immunoproliferative small intestinal disease associated with Campylobacter jejuni,” The New England Journal of Medicine, vol. 350, no. 3, pp. 239–248, 2004.
- N. Uemura, S. Okamoto, S. Yamamoto et al., “Helicobacter pylori infection and the development of gastric cancer,” The New England Journal of Medicine, vol. 345, no. 11, pp. 784–789, 2001.
- D. M. Parkin, “Global cancer statistics in the year 2000,” The Lancet Oncology, vol. 2, no. 9, pp. 533–543, 2001.
- M. L. Gillison and K. V. Shah, “Human papillomavirus-associated head and neck squamous cell carcinoma: mounting evidence for an etiologic role for human papillomavirus in a subset of head and neck cancers,” Current Opinion in Oncology, vol. 13, no. 3, pp. 183–188, 2001.
- H. zur Hausen, “Papillomaviruses and cancer: from basic studies to clinical application,” Nature Reviews Cancer, vol. 2, no. 5, pp. 342–350, 2002.
- S. P. Hussain, L. J. Hofseth, and C. C. Harris, “Radical causes of cancer,” Nature Reviews Cancer, vol. 3, no. 4, pp. 276–285, 2003.
- T. Katagiri and N. Takahashi, “Regulatory mechanisms of osteoblast and osteoclast differentiation,” Oral Diseases, vol. 8, no. 3, pp. 147–159, 2002.
- C. M. E. Champagne, W. Buchanan, M. S. Reddy, J. S. Preisser, J. D. Beck, and S. Offenbacher, “Potential for gingival crevice fluid measures as predictors of risk for periodontal diseases,” Periodontology 2000, vol. 31, pp. 167–180, 2003.
- J. Brown, “Mechanisms of cancer invasion of the mandible,” Current Opinion in Otolaryngology & Head and Neck Surgery, vol. 11, no. 2, pp. 96–102, 2003.
- V. N. Bhattathiri and M. K. Nair, “Periodontal space: a major route to bone involvement in oral cancer,” Medical Hypotheses, vol. 34, no. 1, pp. 58–59, 1991.
- D. Kademani, “Oral cancer,” Mayo Clinic Proceedings, vol. 82, no. 7, pp. 878–887, 2007.
- D. M. Laronde, T. G. Hislop, J. M. Elwood, and M. P. Rosin, “Oral cancer: just the facts,” Journal of the Canadian Dental Association, vol. 74, no. 3, pp. 269–272, 2008.
- K. Rosenquist, J. Wennerberg, E.-B. Schildt, A. Bladström, B. G. Hansson, and G. Andersson, “Oral status, oral infections and some lifestyle factors as risk factors for oral and oropharyngeal squamous cell carcinoma. A population-based case-control study in southern Sweden,” Acta Oto-Laryngologica, vol. 125, no. 12, pp. 1327–1336, 2005.
- A. Argiris, M. V. Karamouzis, D. Raben, and R. L. Ferris, “Head and neck cancer,” The Lancet, vol. 371, no. 9625, pp. 1695–1709, 2008.
- J. Califano, P. van der Riet, W. Westra et al., “Genetic progression model for head and neck cancer: implications for field cancerization,” Cancer Research, vol. 56, no. 11, pp. 2488–2492, 1996.
- P. Meisel, B. Holtfreter, R. Biffar, W. Suemnig, and T. Kocher, “Association of periodontitis with the risk of oral leukoplakia,” Oral Oncology, vol. 48, no. 9, pp. 859–863, 2012.