An Illustrated Guide to Oral Histology. Группа авторов. Читать онлайн. Newlib. NEWLIB.NET

Автор: Группа авторов
Издательство: John Wiley & Sons Limited
Серия:
Жанр произведения: Медицина
Год издания: 0
isbn: 9781119669609
Скачать книгу
by DI are weak and prone to breakage and wear.

      1.7.2 Key Identifying Features

      On histological sections, teeth affected by DI show irregular dentinal tubules. In some areas, dentinal tubules can be completely absent. The dentin present can be quite irregular and haphazard and the pulp chamber can be quite small or completely obliterated.

      1.7.3 Clinical Considerations

      Figure 1.15 H and E stained decalcified section showing DD with haphazard coalescent globules of dentin and pulpal obliteration.

Photo depicts H and E stained decalcified section showing DD with the typical water around the boulders appearance.

      1.8.1 Description

      Dentin dysplasia (DD) is a rare genetic disorder that affects the development of dentin, mostly in radicular area. It can affect both dentitions, where the teeth have normal enamel but abnormal dentin with atypical pulp morphology. The first classification of DD was put forward by Witkop in the 1970s with DD divided into two types: DD‐1 (radicular type) and DD‐2 (coronal type) [16]. The teeth affected by DD‐1 present with short, blunt roots with obliterated pulp chambers. In DD‐2, teeth present with discoloration (brown to blue, amber colored, or opalescent), normal roots but enlarged pulp chambers (thistle tube appearance). The pulp chambers of primary teeth in DD‐2 are almost completely obliterated whereas in permanent teeth, they may be partially obliterated.

      1.8.2 Key Identifying Features

      Histologically, irregular dentin with a disturbed tubular pattern, atubular areas, and globular atypical dentin masses inside pulp chambers can be seen.

      1.8.3 Clinical Considerations

      The etiology of this disease is still unclear. Wesley et al. previously proposed that it could be due to a problem with ameloblasts which leads to an abnormal differentiation of odontoblasts, leading to DD [17]. It was also proposed earlier that due to a problem with dental papilla (foci within it becoming calcified), DD develops as a result of less growth and/or obliteration of pulp chambers [18]. The diagnosis is based on clinical examination and radiographs. The teeth affected by DD have esthetic and functional abnormalities [19]. In addition, they are more prone to be mobile and are exfoliated prematurely [19]. The treatment options include stainless‐steel crowns, endodontic therapy (although difficult due to obliteration of pulp chambers), removable dentures, and dental implants [20–22].

      1 1 Berkovitz, B.K.B., Holland, G.R., and Moxham, B.J. (2009). Oral Anatomy, Histology and Embryology. Edinburgh: Mosby/Elsevier.

      2 2 Nait Lechguer, A., Kuchler‐Bopp, S., Hu, B. et al. (2008). Vascularization of engineered teeth. J Dent Res 87 (12): 1138–1143.

      3 3 Luan, X., Ito, Y., and Diekwisch, T.G. (2006). Evolution and development of Hertwig's epithelial root sheath. Dev Dyn 235 (5): 1167–1180.

      4 4 Li, J., Parada, C., and Chai, Y. (2017). Cellular and molecular mechanisms of tooth root development. Development 144 (3): 374–384.

      5 5 Seow, W.K. (2014). Developmental defects of enamel and dentine: challenges for basic science research and clinical management. Aust Dent J 59 (Suppl 1): 143–154.

      6 6 Kwon, H.‐J.E. and Jiang, R. (1854). Development of the teeth. Am J Dent Sci 4 (2): 291–294.

      7 7 Huang, X.F. and Chai, Y. (2012). Molecular regulatory mechanism of tooth root development. Int J Oral Sci 4 (4): 177–181.

      8 8 Wang, X.P. (2013). Tooth eruption without roots. J Dent Res 92 (3): 212–214.

      9 9 Chaudhary, M., Dixit, S., Singh, A., and Kunte, S. (2009). Amelogenesis imperfecta: report of a case and review of literature. J Oral Maxillofac Pathol 13 (2): 70–77.

      10 10 Crawford, P.J., Aldred, M., and Bloch‐Zupan, A. (2007). Amelogenesis imperfecta. Orphanet J Rare Dis 2: 17.

      11 11 Chen, C.F., Hu, J.C., Bresciani, E. et al. (2013). Treatment considerations for patient with amelogenesis imperfecta: a review. Braz Dent Sci 16 (4): 7–18.

      12 12 Barron, M.J., McDonnell, S.T., Mackie, I., and Dixon, M.J. (2008). Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia. Orphanet J Rare Dis 3: 31.

      13 13 Gama, F.J.R., Corrêa, I.S., Valerio, C.S. et al. (2017). Dentinogenesis imperfecta type II: a case report with 17 years of follow‐up. Imaging Sci Dent 47 (2): 129–133.

      14 14 Sapir, S. and Shapira, J. (2001). Dentinogenesis imperfecta: an early treatment strategy. Pediatr Dent 23 (3): 232–237.

      15 15 Subramaniam, P., Mathew, S., and Sugnani, S.N. (2008). Dentinogenesis imperfecta: a case report. J Indian Soc Pedod Prev Dent 26: 85–87.

      16 16 Kim, J.W. and Simmer, J.P. (2007). Hereditary dentin defects. J Dent Res 86 (5): 392–399.

      17 17 Wesley, R.K., Wysoki, G.P., Mintz, S.M., and Jackson, J. (1976). Dentin dysplasia type I. Clinical, morphologic, and genetic studies of a case. Oral Surg Oral Med Oral Pathol 41 (4): 516–524.

      18 18 Logan, J., Becks, H., Silverman, S. Jr., and Pindborg, J.J. (1962). Dentin dysplasia. Oral Surg 15: 317.

      19 19 Komlós, G., Joób‐Fancsaly, Á., Pataky, L. et al. (2015). Difficulties in differential diagnosis of dentin dysplasia. Case report. Fogorv Sz 108 (2): 53–56.

      20 20 Byahatti, S.M. (2013). Dentin dysplasia type I: a rare case report. Int J Oral Health Sci 3: 57–60.

      21 21 Ravanshad, S. and Khayat, A. (2006). Endodontic therapy on a dentition exhibiting multiple periapical radiolucencies associated with dentinal dysplasia type 1. Aust Endod J 32 (1): 40–42.

      22 22 Muñoz‐Guerra, M.F., Naval‐Gías, L., Escorial, V., and Sastre‐Pérez, J. (2006). Dentin dysplasia type I treated with onlay bone grafting, sinus augmentation, and osseointegrated implants. Implant Dent 15 (3): 248–253.

      Конец ознакомительного фрагмента.

      Текст предоставлен ООО «ЛитРес».

      Прочитайте эту книгу целиком, купив полную легальную