Color Atlas of Oral Diseases in Children and Adolescents. George Laskaris

Color Atlas of Oral Diseases in Children and Adolescents - George Laskaris


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A small amount of mucous secretion may accumulate at the depth of the pits, and the lip may be enlarged and swollen.

      • Occasionally, a fistula may coexist.

      • The diagnosis is based on clinical criteria.

       Treatment

      • Surgical correction for cosmetic purposes.

       Definition

      • Double lip is a malformation that may be present at birth or later in life.

       Etiology

      • It may be congenital due to the failure of the pars glabrosa and the pars villosa to fuse along the horizontal sulcus during lip formation.

      • Acquired double lip is one of the main components of Ascher’s syndrome (double lip, blepharochalasis and goiter).

       Occurrence

      • Rare.

       Localization

      • Often the upper lip, and less frequently the lower lip.

       Clinical features

      • Clinically, it is characterized by an asymptomatic, protruding horizontal fold on the mucosal surface of the lip.

      • Typically, the double lip is visible during speech or smiling, or when the lips are tensed (Figs. 2.12, 2.13).

      • The diagnosis is based on clinical criteria.

       Treatment

      • Mild cases require no treatment.

      • Severe cases require surgical correction for cosmetic purposes.

      

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      Fig. 2.9 Thick and long central frenulum of the upper lip

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      Fig. 2.10 Thin and long central frenulum of the lower lip

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      Fig. 2.11 Bilateral congenital lip pits

       Definition

      • Fordyce’s granules are a normal anatomical variation, characterized by the presence of ectopic sebaceous glands in the oral mucosa.

       Etiology

      • Developmental.

       Occurrence

      • They present in about 20–30% of children and adolescents.

      • About 80% of adults have Fordyce’s granules.

       Localization

      • Upper lip, buccal mucosa, retromolar area, anterior tonsillar pillar.

       Clinical features

      • Clinically, Fordyce’s granules present as multiple yellow or whitish-yellow, slightly raised, tiny pinhead-sized spots that are well circumscribed (Fig. 2.14).

      • Solitary enlarged Fordyce’s granules may also be seen (Fig. 2.15).

      • The granules are asymptomatic, and come to the patient’s attention by chance.

      • The diagnosis is usually based on clinical criteria.

       Laboratory tests

      • Histopathological examination reveals normal collections of sebaceous glands without hair follicles.

       Differential diagnosis

      • Candidiasis

      • Lichen planus

      • Leukoplakia

       Treatment

      • No treatment is required.

       Definition

      • Exostoses are developmental harmless bony overgrowths that may affect the jaws.

       Etiology

      • Unknown. Genetic and environmental factors may be involved in their development.

       Occurrence in children

      • Rare. The lesions are usually first noticed after 20 years of age.

       Localization

      • Midline of the hard palate (torus palatinus).

      • Lingual surfaces of the mandible, usually in the premolar region (torus mandibularis).

      • Buccal surface of the maxillary and/or mandibular alveolar ridge (buccal exostoses).

       Clinical features

      • Clinically, exostoses present as bony, hard nodules covered by normal mucosa (Fig. 2.16).

      • The number and size of the lesions vary considerably.

      • Rarely, the overlying mucosa may be ulcerated due to mechanical trauma.

      • The lesions grow slowly, and are asymptomatic.

      • The diagnosis is based on clinical criteria.

       Treatment

      • No treatment is required. Surgical excision is indicated only when it is necessary to fit a prosthesis.

      

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      Fig. 2.12 Double upper lip

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      Fig. 2.13 Double lower lip

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      Fig. 2.14 Multiple Fordyce’s granules on the buccal mucosa and retromolar area

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      Fig. 2.15 Solitary hypertrophic Fordyce’s granules on the buccal mucosa

       Definition

      • Facial hemiatrophy, or Parry–Romberg syndrome, is a degenerative disorder characterized by atrophic changes of the deeper structures (e.g. fat, muscle, cartilage, and bone) involving one side of the face.

       Etiology

      • Unknown.

       Occurrence

      • Rare. The disease usually starts in


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