Clinical and morphological characteristics of enamel during pigment hypoplasia of tooth tissues.

Authors

  • Yu. V. Silenko Ukrainian Medical Stomatological Academy, Poltava, Ukraine
  • G. A. Eroshenko Ukrainian Medical Stomatological Academy, Poltava, Ukraine
  • I. V. Zhivotovsky Sumy State University, Ukraine
  • E. V. Kuzenko Sumy State University, Ukraine

DOI:

https://doi.org/10.26641/1997-9665.2018.4.78-83

Keywords:

enamel pigment dystrophy, enamel, dentin-enamel border

Abstract

Background. Dystrophic changes in enamel and dentin occur as a result of metabolic disturbances in the hard tissues of the tooth and are characterized by its insufficient formation and mineralization, or excessive accumulation of pigments in the form of spots. The accumulation of pigment (qualitative and quantitative) is irreversible, that is, pigmentary dystrophy has no reverse development and remains in the enamel for life. Objectivе. To analyze the structural changes in tooth enamel in case of pigmentary dystrophy. Methods. After extraction, the teeth were embedded with Epon-812 epoxy. After polymerization, the obtained block was cut with a separating disk on thin sections 0.25 mm thick, an aluminum layer was applied to the preparations in vacuum and examined on a scanning electron microscope REM - 102E with an accelerating voltage of 30 kV. Results. It has been established that in case of chronic discolorites the enamel is partially fragmented, the phenomena of lysis of the enamel are determined. Lacunae are observed on the enamel-dentin border. Enamel preparations with congenital discolorations revealed a thickening of enamel prisms, mosaic expressiveness of Retzius lines. In exogenous pigmentary dystrophy, the main changes are established on the enamel surface. The phenomena of focal fragmentation, diffuse thinning of enamel prisms (atrophic changes) were observed. In endogenous pigmental dystrophy, the main changes are determined by the enamel-dentin boundary. Prisms are thinned and fragmented. Conclusion. Congenital dystrophy of pigment has a diffuse nature and affects the entire thickness of the enamel, which is caused by disorders in the process of histogenesis. With acquired discolorites, the localization of pathological changes depends on the etiology - endogenous, or exogenous. In endogenous pigmental dystrophy, morphological changes are found in the surface layers of enamel, developing as a result of disruption of the tertiary mineralization process, which create favorable conditions for the penetration of pigments by reducing the content of inorganic substances. In endogenous pigmental dystrophy, major changes develop in the deep layers of enamel adjacent to the dentine-enamel border. The source of pigment in this case is enamel spindles, which have a low content of inorganic substances and penetrate into the enamel on 1/3 of its thickness.

References

  1. Borovski EV, Granin AV, Onishchenko SP. [Changes of the hard dental tissues in caries in the stage of pigment spot]. Stomatologiia. 1968;47(4):16-9. Russian. PubMed PMID: 5245264.
  2. de Krom CJ, van Waas MA, Oosterveld P, Koopmans AS, Garrett NR. The oral pigmentation chart: a clinical adjunct for oral pigmentation in removable prostheses. Int J Prosthodont. 2005;18(1):66-70. PubMed PMID: 15754895.
  3. Amaral TH, Guerra Cde S, Bombonato-Prado KF, Garcia de Paula E Silva. Tooth pigmentation caused by bilirubin: a case report and histological evaluation. Spec Care Dentist. 2008 Nov-Dec;28(6):254-7. doi: 10.1111/j.1754-4505.2008.00048.x.
  4. Nedzinskiene E, Drukteinis S, Peciuliene V, Maneliene R. The appearance of root canal surfaces in teeth previously treated using resorcinol-formaldehyde resin: a preliminary SEM investigation. Stomatologija. 2016;18(3):92-7. PubMed PMID: 28386052.
  5. Sommer S, Kramer PF, Magagnin K, Tovo MF. Unusual case of green pigmentation in human teeth resulting from neonatal hyperbilirubinemia. Gen Dent. 2008;56(5):e21-3. PubMed PMID: 21444267.
  6. Dong Q, Wu H, Dong G, Lou B, Yang L, Zhang L. The morphology and mineralization of dental hard tissue in the offspring of passive smoking rats. Arch Oral Biol. 2011;56(10):1005-13. doi:10.1016/j.archoralbio.2011.02.017. PubMed PMID: 21420662.
  7. Khunkar SJ, Utaka S, Hariri I, Sadr A, Ikeda M, Nakashima S, Nikaido T, Tagami J. Formation and characterization of hypermineralized zone beneath dentine lesion body induced by topical fluoride in-vitro. Arch Oral Biol. 2015 Apr; 60(4):574-81. doi: 10.1016/j.archoralbio.2015.01.001. PMID: 25616245.
  8. Ozturk M, Karacelebi E, Gungor K, Coskun S, Boysan E. Evaluation of oxidative events and copper accumulatıon in oral tissues of patients wıth Wilson's disease: three case report. Int J Clin Exp Pathol. 2015;8(4):3943-5. PMID: 26097579; PMC4466966.
  9. Melo ME, Silva CA, de Souza Gomes WD, da Silva VF, Brandini DA, Poi WR, Castilho LR, Sonoda CK, Panzarini SR. Immediate tooth replantation in rats: effect of systemic antibiotic therapy with amoxicillin and tetracycline. Clin Oral Investig. 2016;20(3):523-32. doi:10.1007/s00784-015-1534-0. PMID: 26205067.
  10. Schemel-Suárez M, López-López J, Chimenos-Küstner E. Dental pigmentation and hemochromatosis: A case report. Quintessence Int. 2017;48(2):155-159. doi:10.3290/j.qi.a37385. PMID: 27981269.
  11. Wakasa M, Nakanishi K, Manago K, Isobe T, Eshita Y, Okamoto M, Isshiki T. Fine structure of tooth enamel in the yellowing human teeth: SEM and HRTEM studies. Microsc Res Tech. 2016;79(1):14-22. doi:10.1002/jemt.22600. PMID: 26768788.
  12. Moreira JC, Gallinari Mde O, Rahal V, Fagundes TC, Santos PH, Moura MR, Briso AL. Effect of Dental Pigmentation Intensity on the Transenamel and Transdentinal Penetration of Hydrogen Peroxide. Braz Dent J. 2016;27(4):399-403. doi:10.1590/0103-6440201600838. PMID: 27652700.
  13. Monteiro D, Moreira A, Cornacchia T, Magalhães C. Evaluation of the effect of different enamel surface treatments and waiting times on the staining prevention after bleaching. J Clin Exp Dent. 2017;9(5):e677-e681. doi:10.4317/jced.53712. PMID: 28512546; PMCID: PMC5429481.
  14. Dumont M, Tütken T, Kostka A, Duarte MJ, Borodin S. Structural and functional characterization of enamel pigmentation in shrews. J Struct Biol. 2014; 186(1):38-48. doi:10.1016/j.jsb.2014.02.006. PMID: 24556576.
  15. Yoshida T, Kumashiro Y, Iwata T, Ishihara J, Umemoto T, Shiratsuchi Y, Kawashima N, Sugiyama T, Yamato M, Okano T. Requirement of integrin β3 for iron transportation during enamel formation. J Dent Res. 2012;91(12):1154-9. doi:10.1177/0022034512462722. PMID: 23064962.
  16. Pessoa L, Galvão V, Damante C, Sant'Ana AC. Removal of black stains from teeth by photodynamic therapy: clinical and microbiological analysis. BMJ Case Rep. 2015;2015:bcr2015212276. doi:10.1136/bcr-2015-212276. PMID: 26701991; PMCID: PMC4691879.
  17. Schwandt NW, Gound TG. Resorcinol-formaldehyde resin "Russian Red" endodontic therapy. J Endod. 2003;29(7):435-7. PMID: 12877257.
  18. Petersen RC. Advancing Discontinuous Fiber-Reinforced Composites above Critical Length for Replacing Current Dental Composites and Amalgam. J Nat Sci. 2017;3(2):e321. PMID: 28691101; PMCID: PMC5501257.

How to Cite

Silenko, Y. V., Eroshenko, G. A., Zhivotovsky, I. V., & Kuzenko, E. V. (2018). Clinical and morphological characteristics of enamel during pigment hypoplasia of tooth tissues. Морфологія / Morphologia / Morfologìâ, 12(4), 78–83. https://doi.org/10.26641/1997-9665.2018.4.78-83

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