Laskaris Color Atlas of Oral Diseases in Children and Adolescents

. Zus.-Arb.: George Laskaris 495 Illustrations
1. Auflage 1999
ISBN: 978-3-13-257988-0
Verlag: Thieme
Format: EPUB
Kopierschutz: 6 - ePub Watermark

E-Book, Englisch, 352 Seiten, ePub

Children and adolescents are affected by a large range of diseases with oral manifestations that may not be seen in adults. Such diseases include viral and bacterial infections, but many other conditions as well, for example, after swallowing caustic liquids. As with the author's immensely successful Color Atlas of Oral Diseases, this new work is lavishly illustrated with high-quality color photographs, providing the reader with an at-a-glance diagnostic guide. Succinct texts in tabular form complement the images to help the reader formulate a differential diagnosis and a treatment plan.

George Laskaris

Zielgruppe

Ärzte

Autoren/Hrsg.

Laskaris, George

Fachgebiete

• Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Klinische und Innere Medizin

Inhaltsverzeichnis

Part I Local Diseases
1. Dental Defects
2. Developmental Anomalies
3. Mechanical and Electrical Injuries
4. Chemical Burns and Allergies
5. Foreign-Body Deposits
6. Periodontal Diseases
7. Diseases of the Lips
8. Diseases of the Tongue
9. Non-Odontogenic Cysts
10. Odontogenic Cysts
11. Recurrent Aphthous Ulcers
12. Bacterial Infections
13. Viral Infections
14. Fungal Infections
Part II Systemic Diseases
15. Genetic Disorders
16. Skin Diseases
17. Autoimmune Diseases
18. Gastrointestinal Diseases
19. Hematological Diseases
20. Metabolic Diseases
21. Bacterial Infections
22. Viral Infections
23. HIV Infection and AIDS
24. Systemic Mycoses
Part III Tumors
25. Benign Tumors
26. Fibro-Osseous and Giant-Cell Lesions
27. Malignant Neoplasms

Leseproben

1 Dental Defects

Nick A. Lygidakis
Consultant Paediatric Dentist
DDS, MScD, MScM, DrOdont

Marina G. Laskari
Orthodontist, DDS, MSc
Boston University, USA

Defects in Size

These defects result from various etiological factors acting during the stage of dental morphodifferentiation.

Microdontia

•   Refers to teeth that appear smaller in size compared to normal. Pseudomicrodontia refers to all teeth of an individual appearing smaller than normal, as a result of enlarged jaw dimensions. True microdontia refers to teeth of smaller size in a jaw of normal size (Figs. 1.1, 1.2).

•   Multifactorial. Generalized microdontia is rare, and may be associated with congenital hypopituitarism or exposure to radiation or chemotherapy during dental development. In contrast, localized microdontia is more common, and is frequently followed by hypodontia; it has therefore been suggested that these two defects are controlled by different mutations in the same genes.

•   Syndromes in which microdontia may be seen include the trisomy 21 syndrome, the ectodermal dysplasia syndromes, and the Marshall I, Rieger, focal dermal hypoplasia, Silver-Russell, Williams, Gorlin-Chaudhry-Moss, Coffin-Siris, Salamon, trichorhinophalangeal, odontotrichomelic, neuroectodermal, and dermo-odontodysplasia syndromes.

•   Also a frequent finding in cases of cleft lip and palate.

•   Rare (less than 1%) in primary teeth.

•   More common (2.5%) in permanent teeth.

•   Females more frequently affected than males.

•   Upper laterals.

•   Upper third molars.

•   Usual crown shape or sometimes with tapering (peg or conical) crown, but smaller in size than the range of normal variation.

•   Aesthetic restoration with composites, crowns in severe cases, orthodontic treatment for closure of spaces, if needed.

Macrodontia

•   Refers to teeth that appear larger than the normal size. Some or all teeth may be affected (Fig. 1.3).

•   Multifactorial. Generalized macrodontia is observed in cases of pituitary gigantism, and in individuals with small jaws. Localized macrodontia is observed in cases of unilateral facial hyperplasia, resulting from over-development of tooth buds.

•   Macrodontia may also be associated with congenital hemifacial hypertrophy and some genetic syndromes such as craniofacial dysostosis, otodental svndrome, and Sturge–Weber syndrome.

•   Rare (1.1%) in permanent dentition.

•   Lower third molars and second premolars.

•   Upper central incisors.

•   Frequent bilateral symmetry.

•   Usual tooth morphology with rounded edges, exceeding in size the range of normal variation.

•   Clinically, macrodontia may lead to crowding and potential abnormal teeth eruption as a result of reduced available space in the dental arch.

•   Aesthetic restoration and orthodontic treatment of the potential crowding.

Fig. 1.1 Microdontia of the upper lateral incisors

Fig. 1.2 Microdontia of a lower permolar

Fig. 1.3 Macrodontia of the upper and lower incisors in a patient with otodental syndrome

Conical Teeth

•   Refers to teeth that have a conical shape with a pointed edge.

•   Frequently followed by hypodontia, and for this reason it has been suggested that these two anomalies are controlled by different mutations in the same genes (Fig. 1.4).

•   In the majority of the cases, conical teeth are found in patients with genetic disorders such as ectodermal dysplasia, Rieger, dento-onychodermal and incontinentia pigmenti syndromes.

•   Rare in both permanent and primary teeth (0.2%).

•   Upper incisors.

•   Characteristic conical shape with sharp, pointed edge.

•   Aesthetic restoration with composites, crowns.

Defects in Shape

These defects manifest as a result of various etiological factors acting during the initiation/proliferation and the morphodifferentiation stages of dental development.

Gemination

•   Refers to incomplete division of the tooth bud, resulting in the formation of two partially or completely independent crowns with a shared root (Fig. 1.5). If the division is complete, the anomaly is termed twinning, and results in the formation of a supernumerary tooth, which appears as a minor image of its normal partner.

•   This defect can be found in both the primary and permanent dentitions, and results from various degrees of invagination of the developing dental organ caused by local, systemic, and genetic factors.

•   The genetic factors involved are probably similar to those affecting the dental lamina in cases of hyperdontia.

•   Including fusion, rare in both primary (0.5–1.6%) and in permanent 0.1–0.2% teeth.

•   Males and females equally affected.

•   30–50% of the primary cases are followed by defects in the permanent successors.

•   Upper and lower incisors.

•   Variable, from a minor notch in the incisal edge of a wide crown to almost two separate crowns. Similarly, the pulp chamber and the root canal may be common to both elements, or separate for each one.

•   Potential crowding of the dental arch. Difficulty in the differential diagnosis between gemination and fusion of a normal and supernumerary tooth.

•   Aesthetic restoration with composites, or surgical removal of the supernumerary in cases of twinning. Orthodontic treatment of the potential crowding.

Fig. 1.4 Conical teeth in a patient with hypohidrotic ectodermal dysplasia

Fig. 1.5 Gemination of an upper lateral incisor

Fusion

•   Refers to the union of two discrete tooth buds, resulting in the formation of a tooth with an anomalous shape.

•   The defect is a result of interdental lamina persistence during dental organ development, caused by local factors.

•   Genetic factors have also been implicated, such as autosomal dominant inheritance with reduced penetrance.

•   Including gemination, it is rare in both primary (0.5–1.6%) and permanent (0.1–0.2%) teeth.

•   Ethnic variations result in a higher incidence in some populations.

•   30–50% of the primary cases are followed by defects in the permanent successors.

•   Anterior...

Über Autor(innen)

George Laskaris