Developmental: Soft Tissue and Cysts Flashcards
Hereditary or Genetic
85% - unknown etiology
10% - inherited, any abnormality that is inherited is developmental
5% - known environmental cause (ETOH, thalidomide)
Familial
Runs in families
Congenital
Present at birth, doesn’t imply etiology
Developmental conditions often
A. Present at young age or congenitally
B. Bilaterally symmetrical
C. Asymptomatic
General considerations for developmental conditions
A. Sporadic vs Genetic
B. Isolated vs Generalized
Syndrome: A generalized condition characterized by multiple abnormalities
Agnathia
without jaw development (aplasia)
Micrognathia
Small underdeveloped jaw (hypoplasia)
Macrognathia
Large jaw
Agnathia, Micrognathia, Macrognathia Development
Primary - Developmental
Secondary or acquired - from another disease or condition, eg. tumors, acromegaly, Paget’s disease
Cleft lip and/or palate
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Lip pits
congential malformation often inherited and may be with other anomalies (eg. clefts)
Cheilitis glandularis
Not developmental, infection of minor salivary glands in lower lip, often outdoor workers which thins and drys lips promoting retrograde infection
Variable severity - from slight swelling with dilated, inflamed ductsto significant swelling, pain and deep abscesses ± sinus tracts
Premalignancy ??, shared etiology
Fordyce granules
“ectopic” sebaceous glands develop after puberty. > 80% of population. ↑↑buccal mucosa and often bilaterally symmetrical.
Asymptomatic, superficial yellowish “plaques”
No treatment, recognition only
Fibromatosis gingivae
Inherited, most autosomal dominant
Isolated or with syndromes
Clinically - Asymptomatic, generalized gingival hyperplasia
Treatment: Surgery ? recurrence
Aglossia
Microglossia
Macroglossia
Aglossia – Without tongue development (aplasia)
Microglossia - Small underdeveloped tongue (hypoplasia)
Macroglossia - Enlarged, overdeveloped tongue
Primary - Developmental
Secondary (Acquired) - Tumor, acromegaly etc.