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Odontoestomatología

versão impressa ISSN 0797-0374versão On-line ISSN 1688-9339

Odontoestomatología vol.21 no.33 Montevideo jun. 2019  Epub 01-Jun-2019

https://doi.org/10.22592/ode2019n33a7 

Update

Gingival melanosis: a review of diagnosis and treatment criteria

Yuri Castro-Rodríguez1 
http://orcid.org/0000-0002-9587-520X

1 Facultad de Ciencias de la Salud. Universidad Privada Juan Pablo II. Lima, Perú. yuricastro_16@hotmail.com


Abstract:

Hyperpigmentation of the gingiva is an aesthetic problem for patients with gingival exposure when smiling. The main gingival pigmentation occurs primarily physiologically as a response to trauma, chemicals and ultraviolet radiation. The aim of this study is to review the literature on the criteria for diagnosing and treating gingival pigmentation (melanosis). The author studied articles from the PubMed, EMBASE and SciELO databases from 2005 (January) to present (December 2018). The clinical criteria for diagnosis are based on the severity and extent of the pigmentation on the marginal and attached gingiva. In this way, gingival melanosis is more common at the attached gingiva level, with shades ranging from light chestnut to dark brown. In conclusion, all gingival depigmentation techniques are effective, the differences being cost, healing speed, comfort and degree of postoperative pain.

Keywords: oral pigmentation; melanin; hyperpigmentation; gingiva

Resumen:

La encía hiperpigmentada es un problema estético para los pacientes debido a la exposición gingival al momento de sonreír. La principal pigmentación gingival ocurre de forma fisiológica principalmente como respuesta frente a los traumatismos, sustancias químicas y radiación ultravioleta. En el presente artículo se realizó una revisión bibliográfica sobre los criterios para el diagnóstico y tratamiento de la pigmentación gingival (melanosis). Se exploró los artículos de las bases de datos PubMed, EMBASE y SciELO desde el año 2005 (enero) hasta la actualidad (diciembre del 2018). Los criterios clínicos para su diagnóstico están basados en la severidad y extensión de las pigmentaciones sobre la encía marginal y adherida; de esta forma, la melanosis gingival es más común a nivel de la encía adherida con tonalidades que varían entre el castaño claro y castaño oscuro. Se concluye que todas las técnicas de depigmentación gingival son efectivas; las diferencias se encuentran en el costo, rapidez de cicatrización, confort y grado de dolor posoperatorio.

Palabras clave: Pigmentación oral; melanina; hiperpigmentación; encía

Introduction

“Gingiva” is an umbrella term that refers to the tissues that support the tooth1. It includes the protective gingiva (gum) and the attached gingiva (periodontal ligament, root cement, and the actual alveolar bone). Its main function is to attach the tooth to the bone tissue of the jaws, apart from maintaining the integrity of the surface of the occlusal mucosa2.

One of the macroanatomical features of the gingiva is that healthy gum is usually coral-pink, color which varies depending on the degree of keratinization, the thickness of the gingiva, the degree of vascularization and the presence of melanocytic cells. The color may vary between light chestnut and dark brown.

The gingiva may be pigmented (making it darker) either physiologically or pathologically. The most common pigmentations affecting the protective gingiva are lesions of melanocytic origin, or melanocytic pigmentation (gingival melanosis), occurring due to an excessive deposition of melanin in the basal and suprabasal layers of the epithelium3.

Clinical pigmentation caused by excess melanin is normal, but it is usually a cosmetic problem for some people, mainly those with short lips and high smile lines. On some occasions, gum color conditions impact the end result of an oral rehabilitation treatment, and it is here that the principles of mucogingival surgery can be applied to remove those melanocytic pigmentations and obtain better aesthetic outcomes. However, the clinician must carefully examine the features for the diagnosis and treatment of gingival melanosis. Thus, this review aims to analyze the main diagnostic and treatment considerations necessary to treat melanocytic pigmentations in the mouth; emphasis has been placed on the current and updated concepts obtained from the multiple sources of information consulted.

Method

The author searched for papers from the PubMed, EMBASE and SciELO databases from 2005 (January) to present (December 2018). The research was supplemented with a manual search of the lists of references of each paper selected. Additionally, we obtained papers published in the 1990s and 2000s, and we studied the most relevant ones along those twenty years. The following search words (key words) were selected: ((“Pigmentation disorders” .MeSH. or (“Disorders” and “pigmentation” .all fields.) or (“Melanin precursor” .MeSH. or (“Precursor” and “melanin” .all fields.) or (“surgery” .all fields.) or (“surgical procedures” .MeSH.) or (“oral mucosa”.MeSH.) or (“mucosa” and “oral” .all fields.) or (“Oral pigmentation ” .all fields.) or (“hyperpigmentation” .all fields.) or (“gum” .MeSH.) or (“gingival disease” .MeSH.) or (“disease” and “gingiva” .all fields.) or (“procedures” .all fields.) or (“surgical operating procedures” .all fields.) o (“melanosis” .all fields.) or (“gingival melanosis” .all fields.)). A second search was conducted using health science descriptors (MeSH NLM): ((pigmentation disorders) or (pigmentation) or (skin pigmentation) or (melanosis)). These papers were selected to keep only those which best described the elements of this review. From an initial search of 150 papers, we analyzed 45 papers related to diagnostic and therapy criteria for gingival melanosis.

Development

Gingival melanosis

An alteration characterized by a change in the color of the gingiva, which becomes darker as a result of melanin accumulation. It is probably caused by a genetic condition, and Dummet4 suggests that the degree of pigmentation is relative, and that it depends on chemical, mechanical, and physical stimuli.

Gingival melanosis is more prevalent among dark-skinned people, the French, Filipinos, Arabs and Chinese people5. However, it has been found that it can appear in every social group(6. It is more common in the anterior area of the mandible; in dark-skinned people it is even found in the palatal mucosa and the tongue(6. In 27.5% of the cases it is present in the attached gingiva, the papilla gingiva, the gingival margin, and the alveolar mucosa(7. According to another study, its prevalence is 60.24%(6. Huaman8 studied 130 patients and found a 30% prevalence of light chestnut melanosis, 40.8% of medium chestnut melanosis, and 28.4% of dark chestnut melanosis; 94.5% of the cases showed melanosis in the attached gingiva, and 5.4% in the marginal gingiva.

Diagnostic considerations

Clinically, gingival melanosis appears as dark stains in shades of black, brown, and dark brown, caused by excess melanin deposited on the keratinocytes and/or melanocytes in the basal layer of the epithelium(9.

The degree of pigmentation of the gingiva is usually similar to that of the skin(6, and it depends on melanocyte activity, the number of melanosomes, their degree of dispersion, and the range of degradation of the pigment10.

Physiological pigmentation is usually symmetrical, persistent, and it does not alter the normal architecture of the gingiva. It is more frequent in women than in men(11. Dummet 12 proposes a classification of the color of the melanosis: light chestnut, medium chestnut, and deep chestnut.

Gupta 13) organized the melanocytic stains according to a pigmentation pattern, in order to simplify the diagnosis (Table 1).

Table 1: Melanocytic pigmentation index according to Gupta 

0: No clinical pigmentation
1: mild clinical pigmentation (light brown)
2: moderate clinical pigmentation (medium brown)
3: heavy clinical pigmentation (deep brown, blue-black tissue).

Gingival melanosis can appear in the shape of triangles or lines, or diffuse, and of different color, ranging from black, to dark and light brown. In 2017, the American Academy of Periodontology and the European Federation of Periodontology amended the 1999 classification of periodontal diseases, and proposed a new classification of periodontal and peri-implant diseases14, according to which gingiva color alterations are diagnosed as “gingival pigmentations” (Table 2).

Table 2: Diagnosis of alterations in gingiva color based on the workshop held in 2017. 

Gingival pigmentations
I. Melanoplakia
II. Smoker’s melanosis
III. Drug-induced pigmentations
IV. Amalgam tattoo

Gingival pigmentations can be mistaken for premalignant or malignant lesions such as dysplastic nevi or melanoma15. However, the clinical examination must be thorough, and the patient’s clinical history must be reviewed, as in some cultures, the custom of pigmenting their gingivas with herbs and dyes begins in early childhood16, and this does not correspond to a pathological state of the gingiva, for it is an exogenous form of pigmentation.

There are also systemic conditions that cause pigmentations in the oral cavity, such as the Albright syndrome, Peutz-Jeghers syndrome, neurofibromatosis, and Adisson's disease17.

Other conditions similar to physiological melanosis are: smoker’s melanosis and amalgam tattoos.

Smoker’s melanosis

Patients who are smokers produce more melanin to protect the epithelium from the thermal substances in cigarettes18; these patients usually have melanosis in the anterior area, which presents itself as single stains in the interdental papilla. Araki19 states that smoker’s melanosis depends on the number of cigarettes the individual smokes, and that it depends directly on the dosage. Axell 20 adds that there is more pigmentation in the first year as a smoker, and that it usually diminishes when the person stops smoking. Axell 20 also states that 21.5% of smokers have gingival melanosis.

According to Marakoğlu 21, smoking 5-9 cigarettes a day is enough for a melanocytic stain to appear. Hanioka 22 even found gingival melanosis in smokers’ children, meaning that passive smokers have a predisposition to develop this kind of pigmentations. Sridharan 23 also found solitary pigmentations in the interdental papilla in children exposed to environmental tobacco smoke, and concluded that there is a correlation between the exposure to environmental tobacco smoke and gingival pigmentation. Hanioka 22 found a link between the exposure to environmental tobacco smoke and gingival pigmentation in children with a 5.6 odds ratio, as well as a prevalence of gingival melanosis in 71% of the children assessed; such a high prevalence is associated with the fact that they are passive smokers.

Amalgam tattoo

Focal argyrosis or tattoos are lesions caused by the traumatic implantation of metal particles on soft tissue23. It is the most common exogenous cause of pigmentation, with a 0.4-0.8% frequency in clinical case type studies(24. The reaction of the macrophages to the amalgam makes copper and zinc disappear quickly, while mercury and tin disappear slowly, but this is not the case with silver, which usually persists in the tissue25-27.

Amalgam tattoos can happen when a restoration is removed, during endodontic treatment, or when penetrating the alveoli during tooth extraction28.

Panoramic or periapical radiography is useful to observe the radiopacity of metals, but they are only visible in 25% of the cases as the particles tend to be very small29-30.

Discussion

Many treatments have been proposed to remove melanocytic pigmentations, such as chemical agents (phenol 90% plus alcohol 95%), free grafts, abrasion with rotating or manual tools, cryosurgery with liquid nitrogen, gingivectomies, electrosurgery, and laser(15. Many techniques have become obsolete given their many drawbacks, and others are used less and less. Chemical agents cause major thermal damage31, free grafts are usually not aesthetic(32, rotating tools do not allow the clinician to control the depth of the de-epithelization, gingivectomy is usually linked to bone loss, and the depigmentation it creates is not permanent33.

The term “melanocytic depigmentation” refers to a group of periodontal plastic surgery techniques used to reduce and remove pigmented gingiva(6. One of the first techniques proposed is surgical depigmentation with scalpels, which removes the epithelial tissue leaving the connective tissue to heal by second intention.

The technique known as “mucoabrasion” was proposed by Pérez Fernández in 197734, and consists in making an abrasion with a diamond bur until the melanocytic pigmentation has been removed or is no longer visible. It is a simple, quick technique, with low morbidity for the patient. It is advised to drill past the first bleeding to make sure that the basal layer of the epithelium has been reached35. This technique requires copious irrigation, and it has the disadvantage that it is not possible to control the depth of the de-epithelization36.

Another technique consists in applying laser (an acronym for “Light Amplification by Stimulated Emission of Radiation”), which allows for a high concentration of energy in the area, and it allows for the removal of soft tissue by ablation, but it is not indicated on hard tissue due to its thermal effects37. Laser treatment is a very powerful tool to remove melanocytic stains, it only requires a topical anesthetic, it leaves no scars, it is a fast and simple technique with good results. It usually takes several sessions, and it requires great skill on the part of the operator6.

Laser treatment causes less bleeding and it reduces postoperative pain(6. It has the disadvantage that it causes thermal damage to the bone, for it can penetrate between 2 and 4 millimeters from the surface(38. Er:YAG's laser has been proven to cause less thermal damage; its use must be based on maintaining homeostasis and reducing postoperative pain6. There is not enough evidence to indicate that using laser is better than using a scalpel for depigmentation procedures. The Nd:YAG laser has also had good results, showing a high affinity for melanine or dark pigments39. This laser does not require an anesthetic either, but it is recommended to assess each patient’s pain threshold to decide whether to use an anesthetic or not(3.

Furthermore, cryosurgery uses liquid nitrogen (-196°C) which is applied with soaked cotton wads, or directly on the tissue and left for 20-30 seconds to freeze the epithelium. The epithelium then thaws spontaneously in one minute, necrotizes, and the area re-epithelializes in 3-4 weeks (40.

Most human tissues freeze at -2°C and there is cellular death below -20°C. Cryosurgery uses cryogens to cause cellular death in the epithelium41. Tetrafluoroethane (TFE) and liquid nitrogen are the most widely used cryogens. Shirazi et al.42) evaluated the use of cryosurgery in 15 patients; they found good depigmentation results with a slight degree of recurrence, which was not significant at the end of a 24-month period post surgery. Signh et al.41 compared cryosurgery with TFE versus laser diodes to remove melanocytic pigments, and they found a similar level of satisfaction among the 20 patients under study; after 18 months of control, the TFE showed less postoperative pain (p<0.001) and there was repigmentation in one case in each group.

In one case, Ahmed et al.43 found good results without recurrence 30 months after the treatment with cryosurgery. They added that this technique leads to full regeneration and a sterile inflammatory reaction. Together with laser, it has been recognized for its high aesthetic effectiveness, as well as for the high level of patient satisfaction (41.

A combined technique has also been proposed, which is the combination of the de-epithelization of the basal layer of the attached gingiva with a Nº15 scalpel and the abrasion of the stains in the interdental papilla with fine-grain diamond burs44.

Grados et al.44 state the advantages of this technique: it is a relatively simple operative technique, it is performed in a relatively short operative time, it causes little bleeding, it provides comfort to the patients during and after the intervention, it does not require costly instruments or devices, and its results are satisfactory. In a clinical case series, Castro and Grados45 found good aesthetic results two years after the application of this technique; they add that the repigmentation index is low at the end of the period assessed.

Conclusions

Gingival melanosis is not a pathological problem for most patients; it is a cosmetic problem for people with high smile lines and gingiva exposure. It appears in the form of pigmented lesions which range from light chestnut to dark brown, they are more prevalent in dark-skinned people, but they can be present in every social group. The main gingival depigmentation techniques include gingivectomy, mucoabrasion, laser, and cryosurgery. All of these techniques are effective to remove melanocytic stains, and the differences between them include the degree of postoperative pain, discomfort, cost, and postoperative complications

Referencias

1. Cho ML, Garant PR. Development and general structure of the periodotium. Periodontol 2000. 2000; 24: 9-27. [ Links ]

2. Selvig KA. Structure and function of the periodontium. Dent. Update. 1991; 18: 292-7. [ Links ]

3. Pavlic V, Brkic Z, Marin S, Cicmil S, Gojkov-Vukelic M, Aoki A. Gingival melanin depigmentation by Er:YAG laser: A literature review. J. Cosmet. Laser. Ther. 2018; 20(2): 85-90. [ Links ]

4. Dummett CO. Clinical observation on pigment variations in healthy oral tissues in the Negro. J. Dent. Res. 1945; 24: 7-13. [ Links ]

5. Tal H, Oegiesser D, Tal M. Gingival Despigmentation by Er bium: YAG La ser: Clinical Observations and Patient Responses. J. Periodontol. 2003; 74(11): 1660-7. [ Links ]

6. Roshna T, Nandakumar K. Anterior esthetic gingival depigmentation and crown lengthening: report of a case. J. Contemp. Dent. Pract. 2005; 6(3): 139-47. [ Links ]

7. Duarte A. Cirugía Periodontal Preprotésica y Estética. 1era ed. Bogotá: Santos Editora; 2004. 225p [ Links ]

8. Huaman EV. Características clínicas de melanosis gingival en pacientes del curso de periodoncia de la escuela de Estomatología de la Universidad Nacional de Trujillo. Tesis de bachiller.Trujillo. Facultad de Estomatología, Universidad Nacional de Trujillo; 2013. 54p [ Links ]

9. Ipek H, Kirtiloglu T, Diraman E, Acikgoz G. A comparison of gingival depigmentation by Er:YAG laser and Kirkland knife: osmotic pressure and visual analog scale. J. Cosmet. Laser. Ther. 2018:1-4. [ Links ]

10. Janiani P, Bhat PR, Trasad VA, Acharya AB, Thakur SL. Evaluation of the intensity of gingival melanin pigmentation at different age groups in the Indian population: An observational study. J. Indian. Soc. Pedod. Prev. Dent. 2018;36(4):329-33. [ Links ]

11. Tamizi M, Taheri M. Treatment of severe physiologic gingival pigmentation with free gingival autograft. Quintessence. Int. 1996; 27:555-8. [ Links ]

12. Dummett CO, Bolden TE. Post-surgical clinical repigmentation of the gingiva. Oral. Surg. Oral. Med. Oral. Pathol. 1963;16: 353-6. [ Links ]

13. Gupta G.The labial melanotic macule A review of 79 cases. Br. Dent. Dermatologyc. 1964; 136: 772-75. [ Links ]

14. Corteillini P, Bissada NF. Mucogingival conditions in the natural dentition: Narrative review, case definitions, and diagnostic considerations. J Clin Periodontol. 2018;45(Suppl 20):S190 S198. [ Links ]

15. León SM, Faria H, Pérez L. Despigmentación gingival: Procedimiento quirúrgico. Reporte de un caso. Ciencia. odontológica. 2005; 2(2): 127- 32. [ Links ]

16. Rawal SY, Burrell R, Hamidi CS, Kalmar JR, Tatakis DN. Diffuse pigmentation of maxillary attached gingiva: four cases of the cultural practice of gingival tattoo. J. Periodontol. 2007;78 (1):170-6. [ Links ]

17. Abdo JM, Pérez ET, Bernal FS, Dzib JS. Síndrome de Peutz-Jeghers. Rev. Med. Hosp. Gen. Mex. 2005; 68 (2): 99-105 [ Links ]

18. Kato T, Mizutani S, Takiuchi H, Sugiyama S, Hanioka T, Naito T. Gingival Pigmentation Affected by Smoking among Different Age Groups: A Quantitative Analysis of Gingival Pigmentation Using Clinical Oral Photographs. Int. J. Environ. Res. Public. Health. 2017;14(8). pii: E880. doi: 10.3390/ijerph14080880 [ Links ]

19. Araki S, Murata K, Ushio K, Sakai R. Dose-response relationship between tobacco consumption and melanin pigmentation in the attached gingiva. Arch. Environ. Health. 1983; 38(6):375-8. [ Links ]

20. Axéll T, Hedin CA. Epidemiologic study of excessive oral melanin pigmentation with special reference to the influence of tobacco habits. Scand. J. Dent. Res. 1982;90 (6): 434-42. [ Links ]

21. Marakoglu K, Gürsoy UK, Toker HC, Demirer S, Sezer RE, Marakoglu I. Smoking status and smoke-related gingival melanin pigmentation in army recruitments. Mil. Med. 2007;172(1):110-3. [ Links ]

22. Hanioka T, Tanaka K, Ojima M, Yuuki K. Association of melanin pigmentation in the gingiva of children with parents who smoke. Pediatrics. 2005;116(2):e186-90. [ Links ]

23. Sridharan S, Ganiger K, Satyanarayana A, Rahul A, Shetty S.Effect of environmental tobacco smoke from smoker parents on gingival pigmentation in children and young adults: a cross-sectional study. J. Periodontol. 2011;82 (7):956-62. [ Links ]

24. Laimer J, Henn R, Helten T, Sprung S, Zelger B, Zelger B, Steiner R, Schnabl D, Offermanns V, Bruckmoser E, Huck CW. Amalgam tattoo versus melanocytic neoplasm - Differential diagnosis of dark pigmented oral mucosa lesions using infrared spectroscopy. PLoS. One. 2018;13(11):e0207026. [ Links ]

25. Chavés-Álvarez AJ, Rodríguez-Nevado IM, Argila-Fernández D, Monje-Gil F. Mácula hiperpigmentada en mucosa gingival. Actas. Dermosifiliogr. 2007; 98: 367-8. [ Links ]

26. Owens BM, Johnson WW; Schuman NJ. Oral amalgam pigmentations (tattoos): a retrospective study. Quintessence. Int. 1992; 23: 805-10. [ Links ]

27. Tavares TS, Meirelles DP, de Aguiar MCF, Caldeira PC. Pigmented lesions of the oral mucosa: A cross-sectional study of 458 histopathological specimens. Oral. Dis. 2018; 24(8):1484-91. [ Links ]

28. Hartman LC, Natiella JR, Meenaghan MA. The use of elemental microanalysis in verification of the composition of presumptive amalgam tattoo. J. Oral. Maxillofac. Surg. 1986; 44(8): 628-33. [ Links ]

29. Eley BM, Garrett JR. Tissue reactions to the separate implantation of individual constituent phases of dental amalgam, including assessment by energy dispersive X-ray microanalysis. Biomaterials. 1983; 4(2): 73-80. [ Links ]

30. Mohr W, Gorz E. Association of silver granules with elastic fibers in amalgam reaction of mouth mucosa. HNO. 2001; 49(6):454-7. [ Links ]

31. Hasegawa A, Okagi H. Removing melanogenous pigmentation using 90 percent phenol with 95 percent alcohol. Dent. Outlook. 1973;42: 673-6. [ Links ]

32. Tamizi M, Taheri M. Treatment of severe physiologic gingival pigmentation with free gingival autograft. Quintessence. Int. 1996; 27:555-8. [ Links ]

33. Bergamaschi O, Kon S, Doine AI, Ruben MP. Melanin repigmentation after gingivectomy: A 5-year clinical and transmission electron microscopic study in humans. Int. J. Periodontics. Restorative. Dent. 1993;13: 85-92 [ Links ]

34. Pérez-Fernández A. Pigmentaciones melánicas gingivales. Tratamiento mediante mucoabrasión. Cirugía. Plástica. Ibero- Latinoamer. 1977; 3: 57-9. [ Links ]

35. Mesa FL, García MO, López LC, Aneiros CJ, O´Valle RF. Tratamiento de la melanosis gingival mediante mucoabrasión. Estudio inmunohistoquímico en un paciente con pigmentaciones melánicas múltiples. Periodoncia. 2001; 11 (5): 383-90. [ Links ]

36. Murthy MB, Kaur J, Das R.Treatment of gingival hyperpigmentation with rotary abrasive, scalpel, and laser techniques: A case series. J. Indian. Soc. Periodontol. 2012; 16(4): 614-9. [ Links ]

37. Englard S, Seifter S. The biochemical functions of ascorbic acid. Ann. Rev. Nutr. 1986; 6: 365-406. [ Links ]

38. Spencer P, Cobb CM, Wieliczka DM, et al. Change in temperature of subjacent bone during soft tissue laser ablation. J. Periodontol. 1998;69: 1278-82. [ Links ]

39. Goldstein A, White JM, Pick RM. Clinical applications of the Nd:YAG laser. In: Miserendino LJ, Pick RM, eds. Lasers in Dentistry. 1era ed. Chicago: Quintessence Company; 1995. 126p [ Links ]

40. Hasegawa A, Okagi H. Removing melanogenous pigmentation using 90 percent phenol with 95 percent alcohol. Dent. Outlook. 1973; 42: 673-6. [ Links ]

41. Singh V, Bhat SG, Kumar S, Bhat M. Comparative Evaluation of Gingival Depigmentation by Diode Laser and Cryosurgery Using Tetrafluoroethane: 18-Month Follow-Up. Clin. Adv. Periodontics. 2012; 2: 129-34. [ Links ]

42. Shirazi AS, Moeintaghavi A, Khorakian F, Talebi M. Treatment of gingival physiologic pigmentation in adolescents by liquid nitrogen cryosurgery: 24-month follow-up. Int. J. Periodontics. Restorative. Dent. 2012; 32(4):e142-6. [ Links ]

43. Ahmed SK, George JP, Prabhuji ML, Lazarus F. Cryosurgical Treatment of Gingival Melanin Pigmentation -A 30-Month Follow-Up Case Report. Clin. Adv. Periodontics. 2012; 2:73-8. [ Links ]

44. Grados SP, Castro YR, Bravo FC. Consideraciones clínicas en el tratamiento quirúrgico periodontal. 1era ed. Caracas: AMOLCA; 2014. 165p. [ Links ]

45. Castro RY, Grados PS. Tratamiento de la melanosis gingival y evaluación de la repigmentación melánica. Reevaluación clínica al cabo de 2 años. Rev Clin Periodoncia Implantol Rehabil Oral. 2015; 8(2):139-43. [ Links ]

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