References

Castro MV, Santos NC, Ricardo LH. Assessment of the “golden proportion” in agreeable smiles. Quintessence Int. 2006; 37:597-604
Gupta KK, Srivastava A, Singhal R, Srivastava S. An innovative cosmetic technique called lip repositioning. J Indian Soc Periodontol. 2010; 14:266-269
Newman MG, Takei H, Klokkevold PR, Carranza FA., 11th edn. Los Angeles: Elsevier; 2011
Kathariya R, Pradeep AR. Split mouth de-epithelization techniques for gingival depigmentation: a case series and review of literature. J Indian Soc Periodontol. 2011; 15:161-168
Mahendra M, Gupta V, Singh N, Singh GP. Gingival depigmentation – a case report. Asian J Oral Health Allied Sci. 2012; 2:87-90
Roshna T, Nandakumar K. Anterior esthetic gingival depigmentation and crown lengthening: report of a case. J Contemp Dent Pract. 2005; 6:139-147
Dummett CO. Oral tissue color changes (I). Quintessence Int. 1979; 10:39-45
Almas K, Sadig W. Surgical treatment of melanin-pigmented gingiva: an esthetic approach. Indian J Dent Res. 2002; 13:70-73
Hanioka T, Tanaka K, Ojima M, Yuuki K. Association of melanin pigmentation in the gingiva of children with parents who smoke. Pediatrics. 2005; 116:e186-e190
Humagain M, Nayak DG, Uppoor AS. Gingival depigmentation: a case report with review of literature. J Nepal Dent Assoc. 2009; 10:53-56
Bhusari BM, Kasat S. Comparison between scalpel technique and electrosurgery for depigmentation: a case series. J Indian Soc Periodontol. 2011; 15:402-405
Sharath KS, Shah R, Thomas B, Madani SM, Shetty S. Gingival depigmentation: case series for four different techniques. NUJHS. 2013; 3:132-136
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Thakre P, Bhongade ML, Godge P, Jaiswal R. Comparison of efficacy of Acellular Dermal Matrix Allograft with free gingival graft for gingival depigmentation : a clinical study. Heal Talk. 2013; 5:19-23
Tamizi M, Taheri M. Treatment of severe physiologic gingival pigmentation with free gingival autograft. Quintessence Int. 1996; 27:555-558
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Gingival depigmentation by free gingival autograft: a case series

From Volume 44, Issue 2, February 2017 | Pages 158-162

Authors

Vikas V Pakhare

Senior Lecturer, Department of Periodontics, Sharad Pawar Dental College, Datta Meghe Institute of Medical Sciences (DU), Nagpur, Maharashtra State, India (drvikaspakhare@gmail.com)

Articles by Vikas V Pakhare

Pavan Bajaj

Senior Lecturer, Department of Periodontics, Sharad Pawar Dental College, Datta Meghe Institute of Medical Sciences (DU), Nagpur, Maharashtra State, India

Articles by Pavan Bajaj

ML Bhongade

Professor and Head, Department of Periodontics, Sharad Pawar Dental College, Datta Meghe Institute of Medical Sciences (DU), Nagpur, Maharashtra State, India

Articles by ML Bhongade

BS Shilpa

Postgraduate Student, Department of Periodontics, Sharad Pawar Dental College, Datta Meghe Institute of Medical Sciences (DU), Nagpur, Maharashtra State, India

Articles by BS Shilpa

Abstract

A pleasing smile is desired by all, and forms the main focus of aesthetic dentistry. However, pigmented gums can be a major cause of embarrassment for patients, especially those with a gummy smile. Attempts have been made to meet these cosmetic demands by various methods such as using a surgical blade, diamond burs, electrosurgery, cryosurgery or a laser, but with limited results. Therefore, in the present case series, a free gingival autograft was used for treating gingival melanin hyperpigmentation with a follow-up of six months with no signs of repigmentation.

CPD/Clinical Relevance: This review outlines a method of free gingival autograft as a treatment modality for gingival pigmentation.

Article

A pleasing smile is desired by all, and forms the main focus of aesthetic dentistry.1 A smile should ideally demonstrate natural beauty and pigmented gums can be a major cause of embarrassment for patients, especially those with a gummy smile. Discoloured gums can make a patient feel self conscious2 and prevent them from smiling.

The colour of normal healthy gingiva is coral pink. However, it ranges from pale pink to deep bluish purple. These colour variations depend primarily upon the vascular supply, the thickness of epithelium, degree of keratinization, and the presence of melanin pigment-producing cells.3 Melanin, a brown pigment, is the most common natural pigment contributing to endogenous pigmentation of the gingiva. Physiological pigmentation of the oral mucosa (mostly gingiva) is clinically manifested as multifocal or diffuse melanin pigmentation with variable amounts in different ethnic groups worldwide.4 Melanin pigmentation is caused by melanin granules in gingival tissue, which are produced in melanosomes of melanocytes. Melanocytes are primarily located in the basal and suprabasal cell layers of the epithelium. The colour of the oral melanin pigmentation may vary from light to dark brown or black, depending on the amount and distribution of melanin in the tissue.5 The oral pigmentation is due to the activity of melanocytes rather than the number of melanocytes in the tissue.6

Brown or dark pigmentations and discolorations of the gingival tissues, whether physiological or pathological, can be caused by a variety of local and/or systemic factors.7 Oral melanin pigmentation has been mentioned in the literature and is considered to have different aetiologies, including genetic factors, tobacco use, systemic disorders and prolonged administration of certain drugs, especially antimalarial agents and tricyclic antidepressants.8

It has been observed that there is a positive correlation between gingival pigmentation in children and parental smoking. This pigmentation may be induced by the stimulation of melanocytes by stimuli present in tobacco smoke, such as nicotine and benzopyrene.9 Melanin pigmentation of the gingiva occurs in all races. In dark skinned and black individuals, increased melanin production in the skin and oral mucosa has long been known to be a result of genetically determined hyperactivity of their melanocytes. Earlier studies have shown that no significant difference exists in the density of distribution of melanocytes between light skinned, dark skinned and black individuals.10 However, melanocytes of dark skinned and black individuals are uniformly more reactive than in light skinned individuals. This melanin pigmentation causes an unaesthetic or unpleasant smile and is a major issue of concern, specially for individuals who are fair skinned and have a ‘gummy smile’.

Attempts have been made to meet these cosmetic demands by various methods using a surgical blade,11 diamond burs,12 electrosurgery,4 cryosurgery,13 a laser14 and an Acellular Dermal Matrix Allograft (ADMA)15 graft to eliminate these dark patches of pigmentation on facial aspects of gingiva. But all of these techniques have their own disadvantages and limitations, with some being costly and others, like the surgical blade showing repigmentation and ADMA having a risk of an immune reaction. To overcome these drawbacks, free gingival autografts from the palate have been used, as seen in the literature, for the purpose of gingival depigmentation,16 with a relatively long-term follow-up without repigmentation. However, few studies have been mentioned in the literature regarding the effectiveness of free gingival autografts for gingival depigmentation procedures. Therefore, the aim of the present case series was to determine the effectiveness of free gingival autografts from the palate for the treatment of gingival pigmentation and to assess the degree of repigmentation after the procedure.

Methods and materials

Study population

Five systemically healthy female patients aged between 18 to 30 years of age from the outpatient Department of Periodontics, Sharad Pawar Dental College, who were concerned with the unaesthetic appearance of their anterior maxillary gingivae due to melanin hyperpigmentation were treated in this study with free gingival autografts from unpigmented palate. The Dummett Oral Pigmentation Index (DOPI) score was 3 (Figure 1) in all the patients, ie heavy clinical pigmentation (0 – Pink tissue, ie no clinical pigmentation; 1 – Mild light brown tissue, ie mild clinical pigmentation; 2 – Medium brown or mixed brown and pink tissue, ie moderate clinical pigmentation and 3 – Deep brown/blue-black tissue, ie heavy clinical pigmentation). Patients with a habit of smoking, routine use of medications and pregnant or lactating women were excluded from the study. The gingival hyperpigmentation was recorded pre-operatively and 1 week to 6 months post-surgery by measuring the area of hyperpigmentation in square millimetres, which was determined by marking the area of pigmentation on a transparent sheet and then transferring this record onto graph paper. The severity of hyperpigmentation was recorded using Dummett's Oral Pigmentation Index (DOPI). After the completion of surgical procedure, the patients were called next day and after seven days, for an assessment of pain according to the criteria as described by Gedalia et al17 (0 – No pain; 1 – Discomfort but cannot be called pain; 2 – Mild pain; 3 – Moderate pain; 4 – Severe pain) and at 1 week and 6 months post-surgery for an assessment of gingival repigmentation. Written informed consent was taken from each patient before the surgical procedure.

Figure 1. Pre-operative clinical view.

Surgical procedure

Immediately before the surgical treatment, the patients were made to rinse their mouth with 0.2% chlorhexidine gluconate solution (Rexidine®, Indoco Remedies Ltd) for one minute. The area subjected to surgery was anesthetized by infiltration anaesthesia, using local anaesthetic solution 2% xylocaine with 1:10,000 epinephrine.

Preparation of recipient site

Under all antiseptic conditions, after giving local infiltration anaesthesia of Xylocaine (Xicaine®, ICPA Health Products Limited), a shallow horizontal incision was placed using Bard Parker Surgical blade number 15 (Glassvan®, Niraj Industries Pvt Ltd) over the mucogingival junction on the facial aspect maxilla. The incision was extended to the distal line angle of the canine on both left and right side. The recipient bed was prepared by excising the partial thickness flap of the gingiva from the mucogingival junction to the gingival margin (Figure 2) in such a way that the underlying bone surface would remain covered with periosteum and part of the connective tissue (Figure 3).

Figure 2. De-epithelization at recipient site.
Figure 3. Prepared recipient site.

Obtaining a free gingival graft from the donor site

Under antiseptic conditions, after giving local infiltration anaesthesia (Xicaine®), a free gingival graft was harvested from the unpigmented palate between the maxillary first molar and maxillary cuspid. A tin foil template was used on the recipient site to ensure adequate graft size. Using a Bard Parker surgical blade number 15 (Glassvan®), an incision was made in the palate parallel to the maxillary first molar and canine at a distance of approximately 3 mm apical to the gingival margin. A perpendicular incision was then made to establish the width of the graft for covering the entire area of the recipient site (Figure 4). A split thickness section of 1–2 mm graft was excised using Bard Parker Surgical blade number 15 (Figure 5). The graft was then placed in close contact with the recipient site and held in place by absorbable sutures (4/0 Vicryl, Ethicon, Johnson and Johnson Ltd) (Figure 6). Immediately after surgery the sutured graft was covered with tin foil and periodontal dressing was placed on the recipient site and at the donor site. Analgesics Ibuprofen (Brufen 400 mg, Abbott India Ltd) was prescribed twice daily for 5 days and 0.2% Chlorhexidine gluconate mouthwash (Rexidine®) for 21 days. Patients were instructed to avoid brushing over the surgical area and were recalled next day and after 7 days (1 week) to assess for pain and 1 week, 6 weeks and 6 months post-operatively for evaluation of repigmentation.

Figure 4. Incisions at donor site showing connective tissue bed.
Figure 5. Free gingival graft harvested from hard palate.

Results

Five systemically healthy patients presenting with diffuse gingival pigmentation in the maxillary anterior region from distal of left canine to distal of right canine were included in the study. The gingival melanin pigmentation was treated with a free gingival autograft from the palate. Results were compared with regard to the post-operative pain, and healing after procedure.

During the course of study, the wound healing of the donor as well as the recipient site was free from complications. All of the patients were satisfied with the results of the depigmentation procedure carried out, as none of the grafted sites showed repigmentation during the course of study (Figure 7). In general, all the patients were ready to get the depigmentation carried out in the mandibular anterior region also.

Figure 6. Free gingival graft sutured at recipient site.
Figure 7. Six months post-operative clinical view.

The mean area of pigmentation was 325.6 ± 25.22 sq mm (Table 1) and mean score for severity of pigmentation was 3 at the baseline, whereas no repigmentation was observed during 6 months (Figure 7) of post-surgical follow-up (Table 1). None of the patients complained of pain or discomfort. The assessment of pain post-operatively is described in Table 2. Immediately after the procedure the patients had slight discomfort to mild pain. However, none of the patients had pain or discomfort after 7 days.


Sr no. Patients Pre-surgical values (Area of pigmentation in sq mm) Post-surgical values (Area of repigmentation in sq mm)
1 week 6 week 6 month
1. Case 1 289 0 0 0
2. Case 2 356 0 0 0
3. Case 3 341 0 0 0
4. Case 4 322 0 0 0
5. Case 5 320 0 0 0

Pain Assessment (Gedalia and Brayer criteria)
Immediately post-operative operative operative 1 day post-operative 7 days post-operative
2 3 1
1 1 0
1 0 0
1 0 0
2 2 0

Discussion

Pigmentation of the gingivae may force patients to seek cosmetic treatment. Gingival pigmentation is noticed across all age groups and no gender predilection has been noted. There is no significant difference in the oral pigmentation between males and females.17 Melanin, which is a brown pigment, is the most common natural pigment contributing to endogenous pigmentation of gingiva. It is a non–haemoglobin-derived pigment formed by cells called melonocytes which are dendritic cells of neuroectodermal origin in the basal and spinous layers.18 This physiologic pigmentation is probably genetically determined, but the degree of pigmentation is also partially related to mechanical, chemical and physical stimulation.19 Gingival pigmentation is seen in all races, with a different prevalence in each race and population. The highest rate of gingival pigmentation has been observed in the area of incisors and decreases considerably in the posterior regions.20 It is seen more commonly on the labial surface than on the palatal and lingual surfaces.21 Depigmentation of the gingiva is a periodontal plastic surgical procedure whereby the gingival hyperpigmentation is eliminated. The only indication for depigmentation is a patient's demand for improved aesthetics. Demand for cosmetic therapy of gingival melanin pigmentation is common and various methods have been used for depigmentation, including the scalpel technique of surface de-epithelization, cryosurgery, electrosurgery, lasers and free gingival autografts, each with its own merits and limitations.22 The selection of a suitable technique depends solely upon the clinical experience of the operator, patient compliance and affordability and, lastly, an individual's preference. Although cryosurgery and laser therapy achieve satisfactory results, they require highly sophisticated equipment that is costly. The initial results of de-pigmentation procedure by various methods like a surgical blade are highly encouraging, however, repigmentation is a common problem. The mechanism of repigmentation is not understood but, according to the migration theory,23,24 active melanocytes from the adjacent pigmented tissues migrate to the treated areas, causing repigmentation. This phenomenon seems to be more relevant for depigmentation procedures other than free gingival autografts because, when the non-pigmented palatal mucosa is grafted, the migration of the active melanocytes from adjacent pigmented area is stopped by the basal epithelial layers of the graft. According to Lang and Bernimoulin,25 basal epithelial layers of the graft remain intact and represent the focus of re-epithelization.

In the present case series, free gingival autograft was used for the treatment of gingival pigmentation and the results are in accordance with the previous literature by Tamizi and Taheri 199616 and Thakre et al15 No incidence of repigmentation was observed within 6 months (Table 1) and the post-operative pain (Table 2) was also minimal and subsided completely by the seventh day. However, more long-term and comparative studies are required regarding the efficacy of free gingival graft for the purpose of gingival depigmentation.

Conclusion

In this study, surgical depigmentation using free gingival graft was successful and the patients were satisfied with the results. It is therefore safe to conclude that the procedure adopted was aesthetically acceptable to the patients concerned with no apparent repigmentation in this particular case. All of the patients have reported feeling better about their social appearance, especially when smiling.