Oral Pathology Marathon Flashcards
4 types of pathologies:
Developmental
Hereditary/Genetic
Familial
Congenital
Of the Genetic abnormalities, what % is unknown etiology?
% inherited ?
% known environmental causes?
85%
10%
5%
3 Characteristics of Developmental conditions:
Present at young age/congenital
Bilaterally symmetrical
Asymptomatic
Without jaw development (type of aplasia):
Small, underdeveloped jaw:
Large jaw:
Agnathia
Micrognathia
Macrognathia
Primary Macrognathia:
Secondary (acquired) Macrognathia:
Developmental
tumors, acromegaly, Paget’s
A _______ is characterized by multiple different abnormalities
Syndrome
Teeth come from what germ layer?
Ectoderm
Micrognathia is a type of _____plasia
Hypo
Cleft lip/palate is a _______ anomaly occurring ______
developmental
1st trimester
Cleft lip occurs in 1/____ white births
1/1000
T/F
The etiology of cleft palate is unknown
True
Mutations in cleft lip/palate have been shown in how many genes involved in the development of the palat/lip?
6-12 genes
The lateral palatal shelves fuse anteriorly at the junction with the _______ and fuse posteriorly
Premaxilla
The upper lip (development) is a ______ epithelium
What penetrates/develops into CT and muscle in the upper lip adding bulk?
bilayered
Mesoderm
Where does the mesoderm (forms CT/muscle in upper lip) originate?
Globular portion of median nasal process and Maxillary processes bilaterally
When a cleft forms there is a lack of ______ penetration
Mesoderm
Cleft lip is on the upper lip, off the midline, ___% bilateral
20%
Cleft palate is _____ to the Premaxilla over the _____
Anterior
Alveolar Ridge
T/F
Bifid Uvula is related to Cleft Palate
False
Bifid Uvula is associated with what?
submucosal cleft of muscle
Most common cleft?
2nd most common?
Least common?
Cleft lip with cleft palate
cleft lip
cleft palate
There are over _____ syndromes that include clefting, making up about ____% of all clefting cases.
400
30%
What is the Rule of 10’s in treating cleft lip?
When do you treat cleft Palate?
10 weeks old / 10 lbs / 10 gm% Hb
1.5 years
An oft-missed congenital malformation that may be present with other anomalies:
Lip pits
T/F
Cleft lip is Familial but not Inherited
True
T/F
There isn’t a single gene that gives you clefting, rather 10-12 genes that are involved with the development of your palat
True
T/F
Clefting is the result of abnormal genes plus environmental factors
True
The palatal shelves fuse anteriorly at the junction with the ________
Premaxilla
In Utero, there is nothing in between the bilayered epithelium of the upper lip, but is filled with _______ from the ______ portion of the median nasal process and maxillary process bilaterally
mesoderm
globular
T/F
Chelitis glandularis is developmental
False
*infection salivary glands lower lip
An infection of the salivary glands of the lower lip, often found in those that work outside (promotes retrograde infection):
Chelitis glandularis
T/F
Chelitis glandularis is a premalignant condition
False
*does NOT lead to lower lip cancer
Ectopic sebaceous glands that develop after puberty in 80% of the population
Fordyce granules
Asymptomatic, superficial yellow plaques that are bilaterally symmetric. (an increase of buccal mucosa)
Fordyce granules
T/F
Fordyce granules can be treated
False
no treatment, recognition only
Inherited, mostly Autosomal Dominant that genetically programs the over production of collagen:
Fibromatosis gingivae
Fibromatosis gingivae can be either ____ or found with ______ and is clinically found to be _______ generalized gingival hyperplasia
isolated
syndromes
asymptomatic
T/F
Tx of Fibromatosis gingivae can be surgical but tends to come back
True
No tongue development (an aplasia)
Small, underdeveloped tongue
Enlarged, overdeveloped tongue
Aglossia
Microglossia
Macroglossia
Macroglossia can either be developmental or acquired by what 2 means?
Tumor
Acromegaly
The fusion of the tongue to the floor of the mouth (tongue tied):
Ankyloglossia
Bifid or midline fissure of the anterior 2/3 of the tongue
Cleft Tongue
Deep grooves in the Tongue of unknown etiology (may be genetic) associated with familial pattern of heritability and Age:
Fissured tongue
*not associated with anything systemic
2 terms for Geographic Tongue:
Benign migratory glossitis
Erythema migrans
T/F
Geographic Tongue is developmental
False
Benign Migratory Glossitis (geo tongue) occurs __:__ females to males
On the ___/____ borders of the tongue
Borders color:
2:1
Dorsal/Lateral
Yellowish-Whitish
T/F
Benign Migratory Glossitis (geo tongue) is recommended for biopsy and is infectious
False to both
Benign Migratory Glossitis may burn or hurt (otherwise asymptomatic)
True
Hairy Tongue is hypertrophy of _______ papillae
Filiform
Hairy Tongue has unknown etiology, but name 3 predisposing factors:
Drugs (ABx, H2O2)
Smoking
Radiation Therapy
What is the Tx for Hairy Tongue?
Debridement
CHX
The aging phenomenon of Varix (varicose veins) usually happens where in the mouth?
Also occurs on mouth/lips where color blanches with pressure, but only treated for ______
Ventral Tongue
Esthetics
Using a Glass Slide to determine presence of Varix, blanch through the glass to see it better.
Diascopy
A Lingual Thyroid Nodule is b/c of a breakdown in the ______ Tract with is a ______ invagination starting ________
Thyroglossal Tract
Endodermal
Foramen Cecum
Lingual Thyroid Nodule appears where?
What images?
Tx surgical or ________
Posterior, mid dorsal tongue
Radioactive Iodine
Thyroid Replacement Therapy
2 Lymphoid Tissue oral pathologies:
Hyperplastic Lingual Tonsil
Lymphoepithelial Cyst
Lymphoepithelial Cysts come from _____ ducts
Are a true cyst, meaning they are lined with what?
Present as superficial ______ bumps
***are common in floor of mouth, ventral lateral tongue
Salivary
Epithelium
Yellowish
Tx for Lymphoepithelial Cysts:
Excision
Lymphoepithelial Cysts are Asymptomatic
True
Developmental Lingual Mandibular Salivary Gland Depression:
Located:
Stafne’s Bone Cavity
Below IA canal
In Stafne’s Bone Cavity, the ______ salivary glands develop along the Lingual _____, which produces an indentation
Submandibular
Cortex
T/F
Stafne’s Bone Cavity is inflammatory and changes with time
False
*to both - no swelling, doesn’t change
Stafne’s Bone Cavity is a ______ diagnosis
Radiographic
A group of inherited disorders which program the oral mucosa to abnormally keratinize and generally develop early in life
Genokeratoses
The most common Genokeratosis:
Genetically…
White sponge nevus
autosomal dominant
White sponge nevus
Hereditary benign intraepithelial dyskeratosis
Pachyonychia Congenita
Dyskeratosis congenital
Dariers Diseas - keratosis follicularis
Genokeratoses
The most common form of Developmental Cyst (non-odontogenic)
Incisive Canal Cyst