Periodontal Problems in Kids

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    Periodontal Problems

    inChildren

    Based on a presentation by D. F. Duperon,Chair, Pediatric Dentistry, UCLA(adapted by Callum Durward)

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    Normal Gingiva in Children

    In contrast to adults:

    Round and/or rolledmargins

    Greater sulculardepth

    Epithelium thinner

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    Normal Gingiva in Children cont.

    Less stippling

    Decreased fiber

    density May be pigmented

    Loss of attachment

    and true pocketsrare

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    Periodontal Conditions AffectingChildren and Adolescents

    1. Gingivitis

    Swelling, redness, bleeding

    Not painful

    Plaque induced

    Can be cured by improved oral hygiene(not scaling!)

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    Marginal Gingivitis

    Marginal gingivitis

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    What factors contribute togingivitis in childhood and

    adolescence?LOCAL FACTORS

    Erupting teeth

    Poor oral hygiene

    Restoration overhangs

    Calculus (covered by plaque)

    Crowded teeth

    Mouth breathing

    Orthodontic appliances

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    Mouthbreathing:

    Chronic drying oftissue

    Tacky plaquehardto remove

    Red, inflamed andenlarged gingiva

    May be ENT and/ororthodontic problem

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    Gingivitis cont.

    SYSTEMIC FACTORS

    Hormonal changes eg pregnancy andpuberty

    Diabetesif poorly controlled

    HIV or other immune disorders

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    2. Primary Herpetic Gingivo-Stomatitis (H.S.V. Type 1*)

    @ *Can also be Type 2

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    Symptoms and signs:

    Fever (>38oC)

    Anorexia and malaise

    Sub-mandibular gland swelling Reddened bleeding gingiva

    Multiple vesicles and painful ulcers on gingivaand soft oral tissues

    Lasts 10-14 days

    Primary infections may be mild or sub-clinicalin many children

    @

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    Secondary Herpes Infections

    Virus becomes latent in TG ganglion or basalganglia of brain

    Secondary infection usually presents as

    herpes labialis (cold sore) on the lip Reactivated by eg trauma, heat, hormones,

    sunlight, stress, immunosuppression,(theadmistration of agents that significantly interfere with the ability of theimmune system to respond to antigenic stimulation by inhibiting

    cellular and humoral immunity)concurrent infectionVirus can also infect finger of child or dental

    therapist (if not wearing gloves)

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    Treatment:

    Drink plenty of fluids Soft bland diet Paracetamol

    Antiviral agents (only in some severe cases) egAcyclovir

    Antibiotics for secondary infections Gentle cleaning (may not be able to use toothbrush if

    very painful)can use mouth rinses (eg CHX,

    Difflam or Na bicarbonate/salt)wipe around mouthwith cotton wool if too young to rinse

    IN SEVERE CASES WHERE THE CHILD IS NOTDRINKING (or is immunocompromised) MAY NEEDTO ADMIT TO HOSPITAL

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    3. ANUG

    Acute Necrotizing Ulcerative Gingivitis

    SIGNS ANDSYMPTOMS:

    Ulceration ofinterdental papillae(very painful)

    Foul breath

    Rapid Progression Fever

    Lymphadenopathy

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    Predisposing Factors

    Adolescents and young adults

    Poor OH, calculus

    Stress, poor nutrition, reduced

    immunity eg HIVNote:caused by bacteriagram negative

    fusiform bacilli and spirochaetes

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    ANUG Treatment

    Investigate possibleunderlying medicalproblem

    Local debridement

    Mouth-rinse eg CHXor H202

    Antibiotics: Amoxycillin

    Metronidazole(Flagyl)

    Advanced ANUG

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    4. Gingival Enlargements:

    Drug induced - Dilantin, Cyclosporin, calcium channelblockers (eg Nifedipine), Vigabactrin, Na valproate

    Inflammatorychronic gingivitis

    (puberty/pregnancy) Congenitalhereditary gingival fibromatosis,

    mocopolysaccharoidoses

    Haematologicalleukaemia, aplastic anaemia, vit C

    deficiency (scurvy) Other Conditions

    Eruption cysts

    Opercular flaps

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    Dilantin Hyperplasia

    Dilantin (phenytoin) used in epilepsytreatment

    Incidence: 662%.

    Begins between 2 weeks to 3 months.

    Dose and duration not significant.

    Worsens with poor oral hygiene.

    Occurs only on attached gingiva.

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    Dilantin Hyperplasia

    Adolescent Patient

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    Dilantin Hyperplasia

    Treatment:

    Discontinue Dilantin (Dr must decide ifalternatives acceptable).

    Increase home care. OHI, chlorhexidine, and flossing

    Periodontal surgery.

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    Cyclosporin A

    Often used in children who have hadtransplants

    An anti-rejection drug

    Up to 100% of children on this drug getgingival enlargement

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    Cyclosporin AGingival Enlargement

    Moderate enlargement. Will require surgery.

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    Cyclosporin AGingival Enlargement

    Treatment:

    Discontinue and substitute drug.

    Increased hygiene and plaque control.

    Chlorhexidine mouthwash.

    Gingivectomy.

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    Cyclosporin AGingival Enlargement

    Pre-operative Cyclosporine

    Severity increased by inflammation from brackets

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    Cyclosporin AGingival Enlargement

    Immediate post operative

    One-week post operative Two-week post operative

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    5. Other gingival conditions:a. Eruption Cysts:

    Treatment:

    None if not causing

    problemsusuallyresolvespontaneously

    Incise tissue over

    crown (after topical)refer for this

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    b. Acute Allergic Reaction

    To any allergen:

    Latex

    Nickel Cinnamon and other

    spices

    Treatment: Remove allergen

    Allergy to a type of chewing gum

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    c. Pyogenic Granuloma

    Associated with a local irritant

    Hormonal changes predisposes

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    6. Periodontal bone loss causingpremature tooth loss

    Unexplained premature tooth loss must beinvestigated!

    Childhood Hypophosphatasia. Papillon Le Fevre Syndrome. Cyclic or Familial Neutropenia. Histiocytosis X. Iatrogenic.(originating as a result of professional care; for eg an

    iatrogenic dermatisis ).

    Juvenile periodontitis (pre-pubertal andpubertal forms)

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    a. Childhood Hypophosphatasia

    A metabolic disorder

    Low serum alkaline phosphatase.

    Excretion of Phosphoethanolamine.

    Elevation of serum phosphorus.

    @

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    Hypophosphatasia - Dentalfindings:

    Premature loss ofprimary teeth (oftenbefore age 2).

    Minimalinflammation

    Loss of alveolar

    bone.Abnormal or

    absence ofcementum.

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    b. Papillon Le-Fevre Syndrome

    Hereditary condition

    Premature tooth loss

    Severe inflammationand bone loss

    Both deciduous andpermanent teeth

    Edentulous by 16yrs

    Intensive therapy

    has little effect@

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    Papillon Le-Fevre Syndromeextensive periodontal disease in young patients accompanied by keratotic lesion.

    HyperkeratosisPalmaris.

    HyperkeratosisPlantaris.

    c s ocy os s = anger ans

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    c. s ocy os s = anger ansCell Histiocytosis a group of disease characterized byabnormal histiocyte activity.includes a chronic disseminated type and a chroniclocalized type.

    Includes several diseases.

    All have a proliferation of Langerhans

    cells. Infiltrating histiocytosis of hard and/or

    soft tissues.

    Premature resorption of bone and lossof primary teethon X-ray appear tobe floating in air.

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    Histiocytosis X.

    2 year-old male: Mesial cusp of first perm. molar

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    Histiocytosis X.

    3 year-old male.

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    d. Familial Neutropenias

    Can be chronic, cyclic or intermittentforms

    May suffer from: Recurrent pneumonia.

    Skin and other infections.

    Mouth ulcerations.

    Periodontal disease.

    May improve once they reachadolescence.

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    Chronic (familial) Neutropenia

    8 year-old female

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    Cyclic Neutropenia

    Periodic episodes of fever and oralulcerations.

    Periods of profound neutropenia.

    Onset by 10 years of age.

    19-21 day cycle.

    Course: usually benign.

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    Cyclic Neutropenia

    17 year-old female

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    Acquired Neutropenia

    9 year-old male

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    7. Self-induced Trauma

    3 year-old male

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    Fingernail Trauma.

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    Toothbrush trauma

    Toothbrushing injury in a psychotic child

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    Self Mutilation

    Congenital insensitivity to pain

    Lesch-Nyhan syndrome (hereditary disorder of purinemetabolism characterized by mental retardation ,self-mutilation of the fingers and lip bybiting, impaired renal function ,and abnomal physical development.)

    8 J il P i d i i

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    8. Juvenile Periodontitis(includes pre-pubertal and pubertal forms)

    Prevalence: 0.1 to 0.76%.

    Higher in some ethnic groups eg Black males.

    Localized or generalized. Lack of clinical gingival inflammation.

    Mobility and migration.

    Vertical bone loss especially around first

    molars and incisors.Actinobacillus Actinomycetemcomitans (AA)

    and Capnocytophagia

    @

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    Classic juvenile periodontitis

    Caution! First sign may be mobile teeth!

    Begin periodontal probing in children at10 years of age.

    Check PBWs for bone loss

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    Classic Juvenile Periodontitis

    11 year-old African-American female

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    Classic Juvenile Periodontitis

    Treatment:

    Local debridement.

    Periodontal surgery.

    Antibiotics: Amoxycillin, metronidazole,tetracyclines.

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    Classic Juvenile Periodontitis

    One year post operativePre-opertative