12/7/2015

DEVELOPMENTAL DISTURBANCES OF THE TEETH

Dr. Ibtisam Briek SENUSSI Oral pathology

19.11.2015

Developmental Disturbances

 (1) Size

 (2) Number and Eruption

 (3) Shape/Form

 (4) Defects of Enamel and Dentin

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Size

Microdontia

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Size

 Microdontia

(1) True Generalized Microdontia

(2) Relative Generalized Microdontia

(3) Focal or Localized Microdontia

(1) True Generalized Microdontia

All teeth are smaller than normal

 Occur in some cases of pituitary dawrfism

 Exceedingly rare

 Teeth are well formed

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(2) Relative Generalized Microdontia

 Normal or slightly smaller than normal teeth

 Are present in jaws that are somewhat larger than normal

(3) Focal/Localized Microdontia

 Common condition

 Affects most often maxillary lateral incisior + 3rd molar

 These 2 teeth are most often congenitally missing

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(3) Focal/Localized Microdontia

 Common forms of localized microdontia is that which affects maxillary lateral incisor

 Peg lateral  Instead of parallel or diverging mesial + distal surfaces  sides converge or taper together incisally  forms cone-shaped crown root is frequently shorter than usual

Macrodontia

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Size

 Macrodontia

(1) True Generalized Macrodontia

(2) Relative Generalized Microdontia

(3) Focal or Localized Macrodontia

(1) True Generalized Macrodontia

 All teeth are larger than normal

 Associated with pituitary gigantism

 Exceedingly rare

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(2) Relative Generalized Macrodontia

 Normal or slightly larger than normal teeth in small jaws

 Results in crowding of teeth

 Insufficient arch space

(3) Focal/Localized Macrodontia

 Uncommon condition

 Unknown etiology

 Usually seen with mandibula3rd molars

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Developmental Disturbances

 (1) Size

 (2) Number and Eruption

 (3) Shape/Form

 (4) Defects of Enamel and Dentin

Number and Eruption

 Supernumerary

 Impaction

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Number and Eruption

 Supernumerary  Results from continued proliferation of permanent or primary dental lamina to form third tooth germ

 Teeth may have: • normal morphology • rudimentary • miniature

Number and Eruption

 Supernumerary

 More often in permanent dentition than primary dentition

 More in the maxilla than in mandible

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Number and Eruption

 Supernumerary

 May be impacted erupted or impacted

 Because of additional tooth bulk, it causes:

• Malposition of adjacent teeth

• Prevent their eruption

Number and Eruption

 Supernumerary

 Many are impacted

• Characteristically found in cleidocranial dysostosis

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Number and Eruption

Number and Eruption

 Supernumerary  Mesiodens

 Fourth molar • Maxillary Paramolar • Distomolar or Distodens

 Mandibular Premolar

 Maxillary lateral incisors

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Number and Eruption

 Supernumerary

 Mandibular central incisors

 Maxillary Premolars

Mesiodens

 Most common supernumerary tooth

 Tooth situated between maxillary central incisors Singly , Paired , Erupted or impacted , Inverted

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Mesiodens

 Small tooth  Cone-shaped crown  Short root

Para-molar

 Small + rudimentary

 Situated bucally or lingually to one of the maxillary molars

 Interproximally between 1st + 2nd or 2nd + 3rd maxillary molars

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Distomolar / Distodens

 Molar located distal to molar

Fourth Molar

 2nd most common  Situated distal to 3rd molar  Small rudimentary tooth, but may be of normal size  Mandibular 4th molar also is seen occasionally, but less common than maxillary molar

Distomolar

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Number and Eruption  Anodontia

 lack of tooth development

 absence of teeth

Number and Eruption

 Anodontia

 Complete Anodontia

 Partial Anodontia • • Oligodontia

 Pseudoanodontia

 False Anodontia

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Complete Anodontia

 When all teeth are missing

 Rare

 Often associated with a syndrome known as hereditary ectodermal dysplasia

Hypodontia

 Lack of development of one or more teeth

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Oligodontia

 Lack of development of six or more teeth

Pseudo - Anodontia

 When teeth are absent clinically because of impaction or delayed eruption.

False Anodontia

 When teeth have been exfoliated or extracted

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Number and Eruption

 Impaction

 most often affects the mandibular 3rd molars + maxillary canines

 less commonly: • premolars • mandibular canines • second molar

Number and Eruption

 Impaction

 Occurs due to obstruction from crowding

 From some other physical barrier

 Occasionally, may be due to an abnormal eruption path, presumably because of unusual orientation of tooth germ

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Number and Eruption

 Impaction

 Ankylosis

Ankylosis

 fusion of a tooth to surrounding bone

 with focal loss of periodontal ligament, bone + cementum become inextricably mixed

 cause fusion of tooth to alveolar bone

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Developmental Disturbances

 (1) Size

 (2) Number and Eruption

 (3) Shape/Form

 (4) Defects of Enamel and Dentin

Shape and Form  Crown

 Root

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Shape and Form

 Crown

 Fusion

 Gemination

 Talon’s Cusp

 Leong’s Cusp

Shape and Form

 Crown

 Peg-shaped Lateral

 Hutchinson Incisor

 Mulberry Molar

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Shape and Form

 Root

 Concresence

 Flexion

 Ankylosis

Fusion  Joining of 2 developing tooth germs

 Resulting in a single large tooth structure

 May involve entire length of teeth

 Or may involve roots only, in which case cementum + dentin are SHARED

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Fusion

Gemination

 Fusion of 2 teeth from a single enamel organ  Partial cleavage  Appearance of 2 crowns that share same root canal  Trauma has been suggested as possible cause, the cause is still unknown

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Taurodontism

 Variation in tooth form:

 Elongated crowns

 Apically displaced furcations • Resulting in pulp chambers that have apical occlusal height

Taurodontism

 May be seen as isolated incident in families

 Associated with syndromes such as

 Down syndrome

 little clinical significance

 No treatment is required

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Dens Evaginatus

 Talon’s Cusp

 Leung’s Premolar

Talon’s Cusp

 Well-delineated additional cusp

 Located on the surface of an anterior tooth

 Extends at least half the distance from CEJ to incisal edge

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Leung’s Cusp

 Developmental condition

 Clinically as an accessory cusp or a globule

 Located on occlusal surface between buccal + lingual cusps of premolars

 Unilaterally or bilaterally

Dens Invaginatus (Dens in Dente)

 Deep surface invagination of crown or root that is lined by enamel

 2 forms:  Coronal  Radicular

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Dens Invaginatus (Dens in Dente)

 Depth varies from slight enlargement of cingulum to a deep in-folding that extends to apex

 Historically, it has been classified into 3 major types:

 Type I  Type II  Type III

Dens Invaginatus (Dens in Dente)

 Type I

• Confined to the crown

 Type II • Extends below cemento-enamel junction • Ends in a blind sac • May or may not communicate with adjacent dental pulp

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Dens Invaginatus (Dens in Dente)

 Type III

• Extends through the root • Perforates in the apical or lateral radicular area without any immediate communication with pulp

Peg-Shaped Lateral

 Undersized lateral incisor  Smaller than normal  Occurs when permanent lateral incisors do not fully develop

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Hutchinson’s Incisor

 Characteristic of congenital syphilis

 Lateral incisors are peg-shaped or screwdriver-shaped

 Widely spaced

 Notched at the end

 With a crescent-shaped deformity

Hutchinson’s Incisor

 Notches on their biting surfaces

 Named after Sir Jonathan Hutchinson

 English surgeon + pathologist who 1st described it

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Mulberry Molar

 Dental condition usually associated with congenital syphilis  Characterized by multiple rounded rudimentary enamel cusps on permanent 1st molars

Mulberry Molar  Dwarfed molars with cusps covered with globular enamel growths  Giving the appearance of a mulberry

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Shape and Form

 Root

 Concresence

 Enamel Pearl

 Dilaceration

 Flexion

 Ankylosis

Concrescence

 2 fully formed teeth

 Joined along the root surfaces by cementum

 Noted more frequently in posterior and maxillary regions

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Concrescence

 often involves a 2nd molar tooth in which its roots closely approximate the adjacent impacted 3rd molar

 may occur before or after the teeth have erupted

 usually involves only 2 teeth

Concrescence

 Diagnosis can frequently be established by routine graphic examination

 Often requires no therapy unless union interferes with eruption; then surgical removal may be warranted

 Since with fused teeth, extraction of one may result in extraction of the other

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Enamel Pearls

 Droplets of ectopic enamel

 Or so called enamel pearls

 May occasionally be found on roots of teeth

 Uncommon, minor abnormalities, which are formed on normal teeth

Enamel Pearls

 Occur most commonly in bifurcation or trifurcation of teeth

 May occur on single-rooted premolar as well

 Maxillary molars are commonly affected than mandibular molars

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Enamel Pearls

 Consist of only a nodule of enamel attached to dentin.

 May have a core of dentin containing pulp horn.

 May be detected on radiographic examination.

 May cause stagnation at gingival margin but, if they contain pulp, this will be exposed when pearl is removed

Dilaceration

 Angulation or a sharp bend or curve in root or crown of a formed tooth

 Trauma to a developing tooth can cause root to form at an angle to normal axis of tooth

 Rare deformity

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Dilaceration

 Movement of crown or of the crown and part of root from remaining developing root may result in sharp angulation after tooth completes development

Dilaceration

 Hereditary factors are believed to be involved in small number of cases

 Eruption generally continues without problems

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Flexion

 Deviation or bend restricted just to the root portion

 Usually bend is less than 90 degrees

 May be a result of trauma to the developing tooth

Ankylosis

 Also known as “submerged teeth”

 Fusion of a tooth to surrounding bone

 Deciduous teeth most commonly mandibular 2nd molars  Undergone variable degree of root resorption

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Ankylosis  Have become ankylosed to bone

 This process prevents their exfoliation + subsequent replacement by permanent teeth

 After adjacent permanent teeth have erupted, ankylosed tooth appears to have submerged below level of occlusion

THANKS

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N ATAL T EETH

 These are extra teeth that are present at birth. Cause:

 A developmental disturbance creating intracellular activity during the first stage of tooth development (bud stage) can result in the development of extra teeth.

 The most common natal teeth are lower incisors.

19.11.15

19.11.15 Natal Teeth Treatment:  These teeth are defective and their removal is generally recommended, particularly if mobility poses a threat of aspiration. These teeth also make feeding difficult.

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19.11.15

 These are primary teeth that erupt prematurely (during the first few weeks of life).

Cause:

 Premature tooth eruption.

19.11.15 Neonatal Teeth

Treatment  These teeth are usually normal primary teeth and should be retained. An x-ray will be taken if possible to confirm that these are not extra teeth.

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Shape and Form 19.11.15

• Supernumerary Roots

• Accessory roots are most commonly seen in mandibular canines, premolars and molars ( especially third molar). • Very rare in maxillary anterior teeth & mandibular incisors. • Discovered in routine radiographic examination . • This condition important in extraction of teeth and RCT.

Developmental Disturbances

 (1) Size

 (2) Number and Eruption

 (3) Shape/Form

 (4) Defects of Enamel and Dentin

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Amelogenesis Imperfecta

 also known as:

 Hereditary Enamel Dysplasia  Hereditary Brown Enamel  Hereditary Brow Opalescent Teeth

Amelogenesis Imperfecta

 group of conditions caused by defects in the genes encoding enamel matrix proteins

 genes that encode for enamel proteins:

 amelogenin mutated in  enamelin in patients  others with this condition

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Amelogenesis Imperfecta

 affects both dentition

 deciduous  permanent

 classified based on pattern of inheritance:

 hypoplasia  hypomaturation  hypocalcified

Amelogenesis Imperfecta

 No treatment except for improvement of cosmetic appearance

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Hypoplastic Amelogenesis Imperfecta  inadequate formation of matrix

 enamel is randomly:

 pitted  grooved or very thin  hard + translucent

 defects become stained but teeth are not especially susceptible to caries unless enamel is scanty and easily damaged

Hypoplastic Amelogenesis Imperfecta

 reduced enamel thickness

 abnormal contour  absent interproximal contact points

 Radiographically:

 enamel reduced in bulk  shows thin layer over occlusal + interproximal surfaces

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Hypoplastic Amelogenesis Imperfecta

 dentin + pulp chambers appear normal

 no treatment is necessary

Hypomaturation Amelogenesis Imperfecta

 enamel is normal in form on eruption but:

 opaque  white to brownish-yellow  softer than normal  tends to chip from underlying dentin

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Hypomaturation Amelogenesis Imperfecta

 Radiographically:

 affected enamel exhibits radiodensity similar to dentin

Hypocalcified Amelogenesis Imperfecta

 enamel matrix is formed in normal quantity

 poorly calcified

 when newly erupted:

 enamel is normal in thickness  normal form  but weak  opaque or chalky in appearance

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Hypocalcified Amelogenesis Imperfecta

 with years of function:

 coronal enamel is removed  except for cervical portion that is occasionally calcified better

 Radiographically:

 density of enamel + dentin are similar

Dentinogenesis Imperfecta

 also known as “Hereditary Opalascent Dentin”

 due to clinical discoloration of teeth

 mutation in the dentin sialophosphoprotein

 affects both primary + permanent dentition

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Dentinogenesis Imperfecta

 have blue to brown discoloration

 with distinctive translucence

 enamel frequently separates easily from underlying defective dentin

Dentinogenesis Imperfecta

 Radiographically:

 bulbous crowns  cervical constriction  thin roots  early obliteration of roots canals + pulp chambers

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Dentinogenesis Imperfecta

 Treatment:

 prevent loss of enamel + subsequent loss of dentin through

 cast metal crowns on posterior

 jacket crowns on anterior teeth

Dentinogenesis Imperfecta

 Classification:

 Type I  Type II  Type III

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Type I Dentinogenesis Imperfecta

 occurs in families with Osteogenesis Imperfecta

 primary teeth are more severely affected than permanent teeth

Type I Dentinogenesis Imperfecta

 Radiographically:

 partial or total obliteration of pulp chambers + root canals  by continued formation of dentin  roots may be short + blunted  cementum, periodontal membrane + bone appear normal

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Type II Dentinogenesis Imperfecta

 never occurs in association with osteogenesis imperfecta unless by chance

 most frequently referred to as hereditary opalascent dentin

 only have dentin abnormalities and no bone disease

Type II Dentinogenesis Imperfecta

 Radiographically:

 partial or total obliteration of pulp chambers + root canals  by continued formation of dentin  roots may be short + blunted  cementum, periodontal membrane + bone appear normal

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Type III Dentinogenesis Imperfecta

 “Bradwine type”

 racial isolate in Maryland

 multiple pulp exposures in deciduous not seen in type I or II

 periapical radiolucencies

Type III Dentinogenesis Imperfecta

 enamel appears normal

 large size of pulp chamber is due not to resorption but rather to insufficient + defective dentin formation

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Dentin Dysplasia

 also known as “Rootless Teeth”

 rare disturbance of dentin formation

 normal enamel

 atypical dentin formation

 abnormal pulpal morphology

 hereditary disease

Dentin Dysplasia

 Classification:

 Type I (Radicular Type)

 Type II (Coronal Type)

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Type I (Radicular Type)

 both dentitions are of normal color

 periapical lesion

 premature tooth loss may occur because of short roots or periapical inflammatory lesions

Type I (Radicular Type)

 Radiographically:

 roots are extremely short  pulps almost completely obliterated  periapical radiolucencies: • granulomas • cysts • chronic abscesses

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Type II (Coronal Type)

 color of primary dentition is opalescent

 permanent dentition is normal

 coronal pulps are usually large (thistle tube appearance)

 filled with globules of abnormal dentin

Type II (Coronal Type)

 Radiographically:

(Deciduous)  roots are extremely short  pulps almost completely obliterated

(Permanent)  abnormally large pulp chambers in coronal portion of tooth

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Regional Odontodysplasia

 also known as:

 Odontogenic Dysplasia  Odontogenesis Imperfecta  Ghost Teeth

Regional Odontodysplasia

 one or several teeth in a localized area are affected

 maxillary teeth are involved more frequently than mandibular area

 etiology is unknown

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Regional Odontodysplasia

 teeth affected may exhibit a delay or total failure in eruption

 shape is altered, irregular in appearance

Regional Odontodysplasia

 Radiographically:

 marked reduction in radiodensity  teeth assume a “ghost” appearance  both enamel + dentin appear very thin  pulp chamber is exceedingly large

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Regional Odontodysplasia

 Treatment:

 poor cosmetic appearance of teeth  extraction with restoration by prosthetic appliance

Shell Tooth

 normal thickness enamel

 extremely thin dentin

 enlarged pulps

 thin dentin may involve entire tooth or be isolated to the root

 most frequently in deciduous

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References:

 Books

 Cawson, R.A: Cawson’s Essentials of Oral Oral Pathology and Oral Medicine, 8th Edition • (pages 24-36)  Neville, et al: Oral and Maxillofacial Pathology 3rd Edition • (pages 77-113)  Regezi, Joseph et al: Oral Pathology, Clinical Pathological Correlations 5th Edition • (pages 361-373)  Shafer, et al: A textbook of Oral Pathology, 3rd Edition • (pages 37-69)

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