ORAL PATH: COMPLETE SET Flashcards

1
Q

Linea Alba

A

White Line on Buccal Mucosa
* Plane of occlusion

Focal Hyperkeratosis
* due to chronic friction on mucosa

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2
Q

Traumatic Ulcer

A

Very Common
* Erosion: Incomplete break of epithelium
* Ulcer: Complete break through epithelium (much more painful)

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3
Q

Erosion vs Ulcer

A

Erosion: Incomplete break of epithelium
* only mucosa layer

Ulcer: Complete break through epithleium
* goes into submucosal layer

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4
Q

Chemical Burn

A

White Sloughing Mucosa

Due to:
* Aspirin (topical application)
* Hydrogen Peroxide
* Silver Nitrate
* Phenol

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5
Q

Nicotinic Stomatitis

A

Red Dots= inflammed minor salivary duct openings on hard palate

Only premalignant if “reverse smoking” (lit end in mouth)

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6
Q

Amalgam Tattoo

A

Traumatic implantation of amalgam particles into mucosa
* See clinically & radiographically

Don’t need to biopsy to treat

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7
Q

Smoking-Associated Melanosis

A

Tobaccoo chemicals stimulate melanocytes to make more melanin
* Brown, diffuse, irregular macules
* anterior gingiva
Tx: reversible if stop smoking

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8
Q

Melanotic Macule

A

Benign
* hyperpigmentation in mucous membrane (Basically a freckle)

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9
Q

Peutz-Jeghers Syndrome

A

Melanotic Macule=Freckles (Lips and mouth)

+ Intestinal polyps

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10
Q

Hairy Tongue

A

Elongated Filiform Papillae

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11
Q

Dentifrice-Associated Sloughing

A

Related to SLS (Sodium-Lauryl Sulfate)
* Suggest SLS free toothpaste

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12
Q

Submucosal Hemorrhage

A

Extravascular lesions that DO NOT BLANCH
* Vascular lesions (Hemangiomas, telangiectasias) do blanch

Petechiae: 1mm Hemorrhages
Purpura: Slightly larger than petechiae
Ecchymosis: 1 cm or bigger bruise
Hematoma: Mass of blood w/in tissue, caused by trauma to oral mucosa

Tx: Eliminate the cause

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13
Q

Herpes Simplex Virus

A

Primary Infection:
* Pan-oral (Anywhere in mouth)
* self-limiting
* typically in children
* tx: palliative (symptomatic relief)
* Remains latent in trigeminal ganglion

Recurrent: Keratinized tissue only
1.Herpes labialis: (Cold sore, fever blister)
* vermillion border
2.Recurrent Intraoral Herpes:
* attached gingiva, hard palate
Reactivation is triggered by: Sunlight, stress, or immunosuppresion*

Herpetic Whitlow: Finger Lesions
Herpes Gladiatorum: Head (typically in wrestlers)

Tx: Acyclovir in prodormal period (before it activates)

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14
Q

Varicella Zoster Virus (VZV)

A

Primary Infection: Varicella (aka chickenpox)
* self limiting
* Childhood
* Latent in trigeminal ganglion

Recurrent Infection: Herpes Zoster (Aka Shingles)

tx: Acyclovir

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15
Q

Ramsay Hunt Syndrome

A

Herpes Zoster reactivation –>geniculate ganglion–>affects CN 7 & 8–>Facial paralysis + vertigo +deafness

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16
Q

Coxsackie Virus

A

Hand-Foot-and-Mouth Disease
* Herpangina: Posterior oral cavity (soft palate, throat, & tonsils)

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17
Q

Measles

A

aka Rubeola

Koplik’s Spots:
* red dots/ulcers on buccal mucosa
* before skin rash

Primary infection:
* self-limiting
* Kids

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18
Q

HPV Papilloma

A

aka Wart
* Cause: HPV Strains
* Benign epithelial proliferation of skin or mucosa (Pedunculated or sessile)

Verucca Vulgaris:

Condyloma Acuminatum:

Focal Epithelial Hyperplasia (Heck’s Disease):

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19
Q

Verruca Vulgaris

A

HPV Papilloma type:
* Cause: HPV Strains

Common Skin Wart

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20
Q

Condyloma Acuminatum

A

HPV Papilloma (Wart) Type:
* Cause: HPV 6 and 11

Genital wart, or from oral sex w/someone w/genital warts

Tx: Excise w/high recurrence

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21
Q

Focal Epithelial Hyperplasia

A

Aka Heck’s Disease

HPV Papilloma Type (wart):
* Cause; HPV 13 and 32

Multiple small dome-shaped warts on oral mucosa

“Whole mouth goes to heck”

Tx: Excise w/excellent prognosis

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22
Q

Oral Hairy Leukoplakia

A

Cause: EBV (Epstein-Barr Virus)

White patch on lateral tongue
* DOES NOT wipe off

Opportunistic infection

associated with:
* HIV
* Burkitt’s Lymphoma

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23
Q

Syphillis

A

Cause: Treponema Pallidum (Spirochette bacteria)

Primary Lesion: chancre

Secondary Lesion
* Oral mucous patch
* condyloma latum
* Maculopapular rash

Tertiary Lesion:
* gumma
* CNS & CV involvement

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24
Q

Congenital Syphillis

A

Hutchinsons Triad:
* Notched Incisors
* Mulberry molars
* Deafness
* Ocular Keratitis

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25
Q

Tuberculosis

A

Cause: Inhale Mycobacterium Tuberculosis
* Lung infection then nonhealing chronic oral ulcers

Primary Infection: Ghon Complex

Secondary Infection:: more wide spread lung infection w/cavitation

Miliary Infection: systemic spread

HIV Pts=Higher risk of progressive disease

Tx: Multidrug therapy
* Isoniazid, rifampin, ethambutol)

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26
Q

Gonorrhea

A

Cause: Neisseria gonorrhoeae

Oral manifestations=rare

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27
Q

Actinomycosis

A

Cause: Actinomyces israelii (Filamentous bacteria)
* NOT FUNGAL)

sulfur granules In puss*

types:
* Periapical: Jaw infections
* Cervicofacial: Head and neck infections

Tx: Long term high does Penicillin

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28
Q

Scarlet Fever

A

Cause: Group A Strep (Streptococcus pyrogenes)
* Strep throat becomes systemic

Strawberry tongue:
* White coated tongue w/red fungiform papillae

Tx: Penicillin

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29
Q

Candidiasis

A

aka Thrush

Types:
Pseudomembranous:
* White plaque that rubs off

Atrophic:
* Red

Median Rhomboid Glossitis:
* Loss of lingual papillae (pictured)

Angular Cheilitis:
* Corner of mouth

Tx: Antifunal (Azole or statin)

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30
Q

Aphthous Ulcer

A

Aka Canker Sore

Affeects Nonkeratinized tissue
* Herpes ulcers only on keratinized tissue

2 Forms:
Minor:
* Heal w/o scarring
* Tx: Salt rinse

Major: Aka sutton disease
* Heal w/scarring

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31
Q

What area of the mouth are nonkeratinized

A

Labial/buccal/alveolar mucosa
Floor Of Mouth
Soft palate
Ventral Surface of Tongue (Bottomside)

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32
Q

Behcet’s Syndrome

A

Multisystem vasculitis:
* Oral and genital Aphthous ulcers
* Eye inflammation

Tx: Corticosteroids

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33
Q

Erythema Multiforme

A

Usually on lips

2 Forms:
Minor:
* Herpses simplex hypersensitivity

Major:
* Drug sensitivity
* aka Steven-Johnson Syndrome

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34
Q

Angioedema

A

Allergic reaction to drug or food contact

Diffuse swelling of lips
* (and/or neck & face)

Mediated by IgE & histamines released by mast cells

Tx: Antihistamines

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35
Q

Wegener’s Granulomatosis

A

Allergic reaction to inhaled antigen

Strawberry Gingivitis

Tx: Corticosteroids (prednisone) & cyclophosphamide

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36
Q

Lichen Planus

A

T lymphocytes target & destroy basal keratinocytes
* secondary affect: Sawtooth rete pegs

Forms:
Reticular:
* Wickham striae
* White-lacy; net-like
* more common

Erosive:
* Wickham striae w/red ulceration

Tx: Corticosteroids

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37
Q

Lupus Erythematosus

A

Aka Lupus

Types:
Discoid Chronic:
* Disc-like lesion on fascial skin
* Oral lesions mimic erosive lichen planus

Systemic Acute:
* involves multiple organs
* butterfly rash over bridge of nose
* involves autoantibodies (ANA Test)

Tx: Corticosteroids

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38
Q

Scleroderma

A

Hardened Skin and Connective Tissue

Restrict mouth opening
Uniform widened PDL space

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39
Q

Pemphigus Vulgaris

A

Suprabasilar clefting

Autoantibodies against desmosomes

Bullae –> multiple painful ulcers
* bullae-big fluid filled blister that pops

Positive Nikolsky’s Sign: sloughing of outer skin layer

Tx: Corticosteroids

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40
Q

Pemphigoid

A

O, Old, Opthamlogist
* Subasilar
* Autoantibodies against Hemidesmosomes

Pemphigus= U-bove
Pemphigoid=Below

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41
Q

Leukoplakia

A

Clinical Description, NOT a Diagnosis

White patch that does NOT rub off
* No obvious Clinical Dx

Tx: Mandatory biopsy

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42
Q

Proliferative Verrucous Leukoplakia

A

Clinical Description
* Recurrent & warty
* associated with: HPV 16 & 18 (develop cervical cancer)

High risk of malignant transformation to:
* SCC or
* verrucous carcinoma

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43
Q

Erythroplakia

A

Clinical Description, NOT diagnosis

Red Patch
* higher risk of becoming malignant than leukoplakia (Erythroleukoplakis=highest risk)

Tx: Mandatory Biopsy

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44
Q

Erythroleukoplakia

A

Clinical Description, Not Dx
*Red and white patch

Highest risk for malignant transformation

Tx: Manditory biopsy

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45
Q

Actinic Cheilitis

A

Actinic=Solar
Cheilitis= lip inflammation

cause: sun damage (UV-B especially)

(UV-Bad)

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46
Q

Smokeless Tobacco-Associated Lesion

A

Wrinkly white appearance in vestibule

cause: smokeless tobaccco and additives

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47
Q

What are the high risk sites for oral cancer?

A
  1. Floor of Mouth
  2. Posterior Lateral Tongue
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48
Q

What are the different types of cancer and origin?

A

Carcinoma: Epithelial origin
Sarcoma: mesenchymal (aka CT) origin
Leukemia: Blood
Lymphoma: Lymphatics

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49
Q

Cancer Stages

A

Dysplasia: Pre-cancer

Carcinoma in situa: affects all epithelium layers

Manlignant Neoplasm: Aka Cancer
* invades past the basement membrane
* Local Invasion: Connective Tissue
* Metastasis: Access blood or lymph–>rest of body

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50
Q

Verrucous Carcinoma

A

aka Snuff Dippers Carcinoma

cause:
* HPV 16 & 18
* tobacco

Slow growing malignancy
Tx: Excisision

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51
Q

Squamous Cell Carcinoma

A

Aka Oral cancer, oral SCC

cause: oncogene activation or inactivation of tumor suppressor genes

Increased incidence of oropharyngeal SCC associated w/HPV 16 & 18

5 year survival rate: 50%

Tx: excision or radiation

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52
Q

Plummer-Vinson Syndrome

A

=Mucosal Atrophy
+ Dysphagia (Trouble Swallowing)
+ Iron Deficiency anemia
+ Increased oral cancer risk

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53
Q

Basal Cell Carcinoma

A

Cause: Sun Damage

Rarely Metastasizes

least dangerous cancer

Tx: Surgical excision

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54
Q

Oral Melanoma

A

Malignancy of Melanocytes
* Purple/black lesion

High risk areas:
* Palate
* gingiva

5 year survial rate:
* Skin=65%
* Oral= <20%

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55
Q

Deep Fungal Infections

A

Fungi found in soils

Blastomycosis:
* Northeast US
* inhale spores

Caccidiomucosis:
* Southwest US
* Valley fever

Cryptococcosis:
* West US

Histoplasmosis:
* Midwest US

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56
Q

c

A
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57
Q

Cleft Lip

A

4-6 weeks in utero

No fusion b/w medial nasal process and maxillary process anteriorly

Usually offset, Unilteral

More common in Males

Tx: Surgically repaired at 3-5 months old

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58
Q

Cleft Palate

A

6-8 weeks in utero

No fusion b/w palatal shelves/Medial Nasal Process and Maxillay process posteriorly

Primary Palate: carries lateral incisor to lateral incisor. Why lateral incisors are missing

Complete CP: No fusion of Both Primary & Secondary palates

More common in Females

Surgical Repair: 6-12 months old

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59
Q

Lip Pits

A

Invagination at commissures or midline

Commisural Lip Pits: at corner of mouth

Paramedian Lip Pits: Bilateral midline lips

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60
Q

Van der Woude Syndrome

A

Most common genetic syndrome associated w/Cleft Lip & Palate

Cleft (Lip, palate, or both) + (Paramedial) Lip Pits

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61
Q

Fordyce Granules

A

Ectopic Sebacceous glands

Buccal Mucosa

Benign

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62
Q

Leukoedema

A

White/grey edematous (Fluid Filled) lesion

  • on buccal mucossa (Very common)

Goes away when cheek is stretched

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63
Q

Lingual Thyroid

A

Thyroid TIssue mass at midline base of tongue
*This is where the thyroid tissue orignates during development
* it normally migrates down the neck/trachea to form thyroid gland

located along embryonic path of thyroid descent

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64
Q

Thyroglossal Duct Cyst

A

Midline Neck Swelling

located along embryonic path of thyroid descent

Similar to lingual thyroid, but did not migrate all the way down

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65
Q

Geographic Tongue

A

Aka Benign Migratory Glossitis, Erythema Migrans

White Ring surround central red islands
* migrate

May be associated w/certain foods

occasionally hurt & burn

Tx: None

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66
Q

Fissured Tongue

A

Folds & Furrows of dorsum tongue (Surface)

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67
Q

Melkerson-Rosenthal Syndrome

A

=Fissured Tongue + Granulomatous Cheilitis + Facial Paralysis

Think of it as MELS BELLS
* Bells Palsy=another type of facial paralysis w/facial nerve

Rosy Red
* red affecting lips-cheilitis

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68
Q

Angioma

A

Tumors composed of blood vessels or lymph vessels

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69
Q

Cherry Angioma

A

Red Mole

  • very common
  • Benign
  • small tumor of capillarioes
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70
Q

Hemangioma

A

Congenital Focal Proliferation of capillaries

Most undergo involution as a child, but persistent lesions are excised

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71
Q

Lymphangioma

A

Congenital Focal Proliferation of Lymph Vessels

Oral Lymphangiomas:
* very rare
* purple spots on tongue

On neck=Cystic Hygroma

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72
Q

Sturge-Weber Syndrome

A

=Angiomas of leptomeninges (Arachnoid & pia Mater) + Skin w/CN V distribution

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73
Q

Dermoid Cyst

A

If Above Mylohyoid
* midline floor of mouth mass (Intraoral)
If Below mylohyoid:
* upper neck mass (extraoral)

Contains Adnexal Structures (hair, sebaceous glands)

Doughy Consistency: Main distinguishing feature vs a ranula

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74
Q

Branchial Cyst

A

Lateral neck swelling

Epithelial Cyst w/in lymph node of neck

75
Q

Cysts

A

Have an epithelial lining

76
Q

Oral Lymphoepithelial Cyst

A

Epithelial cyst w/in Lymph nodes of oral mucosa

Common: Palatal or Lingual Tonsils

77
Q

Stafne Bone Defect

A

posterior mandible Radiolucency
* below mandibular/IAN canal

Normal Anatomic Variation: Very severe lingual concavity

78
Q

Nasopalatine Duct Cyst

A

Heart shaped radiolucency in nasopalatine canal

caused by cystification of canal remnants

Tx: Surgical Excision

79
Q

Globulomaxillary Lesion

A

Clinical Term (not a Dx)
* any radiolucency b/w maxillary canine and maxillary lateral incisor

80
Q

Traumatic Bone Cyst

A

Aka Simple Bone Cyst, Idiopathic Bone Cavity

Large radiolucency that scallops around tooth roots

No Epithelial lining (like a Pseudocyst)

Mostly in mandible of teenages
* associated w/jaw trauma

Tx: Aspirate to diagnose (Blood in it), Just monitor

81
Q

Leukoplakia

A

Clinical Description, NOT a Diagnosis

White patch that does NOT rub off
* unknown etiology

Tx: Mandatory biopsy

82
Q

Proliferative Verrucous Leukoplakia

A

Recurrent & warty

associated with: HPV 16 & 18

High risk of malignant transformation to SCC or verrucous carcinoma

83
Q

Erythroplakia

A

Clinical Description, NOT a diagnosis

Red Patch
* higher risk of malignant transformation than leukplakia

Tx: Mandatory Biopsy

84
Q

Actinic Cheilitis

A

Actinic=Solar

Due to sun damage (UVB especially)

85
Q

Smokeless Tobacco-Associated Lesion

A

Wrinkly white appearance in vestibule

due to: smokeless tobaccco and additives

86
Q

What are the high risk sites for oral cancer?

A
  1. Floor of Mouth
  2. Posterior Lateral Tongue
87
Q

What are the different types of cancer?

A

originates from:
Carcinoma: Epithelial Tissue
Sarcoma: mesenchymal (aka CT)
Leukemia: Blood
Lymphoma: Lymphatics

88
Q

Cancer Stages

A

Dysplasia: Pre-cancer

Carcinoma in situa: affects all epithelium

Manlignant Neoplasm: Aka Cancer
* invades past the basement membrane
* Local Invasion: Connective Tissue
* Metastasis: Access to blood or lymph to travel around the body

89
Q

Verrucous Carcinoma

A

cause:
* HPV 16 & 18
* tobacco

Slow growing malignancy
Tx: Excisision

90
Q

Squamous Cell Carcinoma

A

Aka Oral cancer, oral SCC

cause:
* oncogenes
* inactivation of tumor suppressor genes

Increased incidence of oropharyngeal SCC

5 year survival rate: 50%

Tx: excision or radiation

91
Q

Oropharyngeal SCC

A

HPV 16 & 18

92
Q

Plummer-Vinson Syndrome

A

=Mucosal Atrophy + Dysphagia (Trouble Swallowing) + Iron Deficiency anemia + Increased risk of oral cancer

93
Q

Basal Cell Carcinoma

A

Cause: Sun Damage

Rarely Metastasizes

Tx: Surgical excision

94
Q

Oral Melanoma

A

Malignancy of Melanocytes

High risk areas: Palate & gingiva

5 year survial rate:
* Skin=65%
* Oral=20%

95
Q

Fibroma

A

aka Traumatic Fibroma, Irritation Fibroma, Hyperplastic scar

Fibrous hyperplasia of oral mucosa
* Cause: Chronic Trauma or irritation

96
Q

Gingival Hyperplasia

A

aka Gingival Enlargement
CDC concerned about Gingival Hyperplasia

Calcium Channel Blockers:
* Nifedipine
* Amlodipine
* Verapamil

Dilantin: Anticonvulsant/epileptic

Cyclosporine: Immunosuppressant

Tx: Gingivectomy and discontinue drug if possible

97
Q

Dentur-Induced Fibrous Hyperplasia

A

Epulus Fissuratum:
* Base of vestibule
* Cause: Overextended flange of denture

Papillary Hyperplasia:
* hard palate
* cause: Poor denture hygiene

(Angular Cheilitis)

98
Q

Traumatic Neuroma

A

Entangled submucosal mass of:
* neural tissue
* scar

Cause: Nerve Injury
* most common=mental foramen (Mental N.)

99
Q

Multiple Endocrine Neoplasia

A

aka MEN 2B

=Multiple Neuromas (not traumatic)

+ medullary thyroid Cancer

+ Pheochromocytoma of adrenal gland

100
Q

Pyogenic Granuloma

A

Hyperplasia of capillaries=RED color

Cause:
* Chronic trauma or irritation

Gingiva=most commn

101
Q

Nodular Fasciitis

A

Neoplasm of Fibroblasts

easy to eradicate (Opposite of Fibromatosis)
* Rare recurrence

Tx: Excision

102
Q

Fibromatosis

A

Neoplasm of fibroblasts

Difficult to eradicate (opposite of nodular fasciitis)
* high Recurrence

103
Q

Granular Cell Tumor

A

Neoplasm of Schwann Cells

Contain:
* granular cytoplasm
* Pseduoepitheliomatosu Hyperplasia (PEH)-mimics SCC histologically

Dorsal/Anterior tongue=Most common

Congenital Epulis of Newborn
* variant
* on gingiva
* no PEH

104
Q

Schwannoma

A

aka Neurilemmoma

Neoplasm of Schwann Cells

Acellular Verocay bodies in Antoni A Tissue
* Forms a line of scrimmage

105
Q

Neurofibroma

A

Neoplasm of Schwann Cells and Fibroblasts

106
Q

Neurofibromatosis type I

A

Aka Von Recklinghausens Disease (Von FRECKLINGhuasen Disease)

=Multiple Neurofibromas

+ Multiple skin freckles (Cafe au lait spots)

+ Axillary Freckles (Crowe’s sign)

+ Iris freckles (Lisch spots)

neurofibromas can transform to neurofibrosarcomas

107
Q

Leiomyoma

A

Neoplasm of smooth muscle cells

108
Q

Rhabdomyoma

A

Neoplasm of skeletal muscle cells

109
Q

Lipoma

A

Neoplasm of fat cells

buccal mucosa=most common

110
Q

Fibrosarcoma

A

Malignant Proliferation of fibroblasts

111
Q

Neurofibrosarcoma

A

aka Peripheral Malignant nerve sheath tumor

Malignant proliferation of Schwann Cells

112
Q

Kaposi’s Sarcoma

A

Malignant proliferation of endothelial cells

cause: HHV8 (Human Herpes Virus 8)
* Hard Palate
* most commonly seen as complication in AIDs pt

Purple Lesion

113
Q

Leiomyosarcoma

A

Malignant proliferation of smooth muscle cells

114
Q

Rhabdomyosarcoma

A

Malignant prolifeation of Skeletal Muscle cells

115
Q

Liposarcoma

A

Malignant proliferation of Fat cells

116
Q

Mucous Extravasation Phenomenon

A

Cause: Salivary Duct Trauma
* not a true cyst

Mucocele:
* Lower Lip
* Salivary Duct blocked due to trauma

Ranula:
* Floor of mouth

tx: COMPLETE excision of minor gland
* Ranula=Sublingual Gland

117
Q

Mucous Retention Cyst

A

Cause: Sialolith blocks salivary duct
* True Cyst

118
Q

Necrotizing Sialometaplasia

A

Rapidly expanding ulcerative lesion

Cause: ischemic necrosis of minor salivary glands
* due to trauma or local anesthesia

Tx: Palliative
* heals on its own in 6-10 wks

119
Q

Sinus Retention Cyst

A

Aka Antal Pseudocyst

Cause: Salivary Glands blocked in sinus mucosa

Tx: None

120
Q

Sarcoidosis

A

Hyperimmune
* involves granulomas

Triggers:
* Mycobacteria (same as TB)

Primarily a pulmonary disease
* Causes XEROSTOMIA

Tx: Corticosteroids

121
Q

Sjogren’s Syndrome

A

Autoimmune & lymphocyte mediated
* Affects salivary & tear glands

Types:
Primary:
* Keratoconjunctivitis sicca (Dry eyes)
* + Xereostomia

Seconary:
* Primary + another autoimmune disease (Rheumatoid arthritis)

Tx: Symptomatic

122
Q

Pleomorphic Adenoma

A

Most common Benign Salivary gland tumor

comoppsed of:
* mixture of cell types: epithelial & CT
* why its AKA Mixed tumor

Firm rubbery swelling:
Water chest-nut Appearance
Most common site:
* minor salivary gland=palate
* parotid gland=ear

123
Q

Monomorphic Adenoma

A

Benign Salivary Gland tumor

Composed of: 1 type of cell

Includes:
* basal cell adenoma
* canalicular adenoma
* myoepithelioma
* oncocytic tumor

tx: Surgical excision

124
Q

Warthin’s Tumor

A

Benign Salivary Gland Tumor

Composed of:
* Oncocytes(Cells w/XS Mitochondria)
* Lymphoid cells

Most common: Parotid Gland of Older Men

125
Q

Mucoepidermoid Carcinoma

A

Most common Salivary Gland Malignancy

composed of:
* Mucous
* epithelial cells

126
Q

Polymorphous Low-Grade Adenocarcinoma (PLGA)

A

2nd most common Salivary Gland malignancy for minor glands

Adeno=gland

127
Q

Adenoid Cystic Carcinoma

A

Malignant Salivary Gland Tumor

Cribiform or Swiss cheese microscopic pattern

5 year survival=70%
15 year=10% Very Lethal

128
Q

Cysts

A

Cavities lined by epithelium

129
Q

Odontogenic Cysts

A

derived from cells associated w/tooth formation

130
Q

Radicular Cyst

A

Aka Periapical Cyst
Most common odontogenic cyst

Radiolucency at apex
* Always Nonvital tooth

Necrotic pulp –> periapical inflammation
* Acute=Abscess
* Chronic=Granuloma

Epithelial Rests of Malassez (ERM)
* from Hertwig’s Epithelial Root Sheath (HERS)
* encapsulate lesion=forms cyst

Tx: RCT, apicoectomy, or EXt w/curretage

131
Q

Dentigerous Cyst

A

Aka Eruption Cyst

Accumulation of fluid b/w crown & Reduced Enamel Epithelium

Radiolucency attached to CEJ of impacted teeth

Most common: K9s & 3rd molars

Tx: Excision, but might be source of future odontogenic tumor

132
Q

Lateral Periodontal Cyst

A

Most common=mandibular premolar region
* Always vital tooth
* not centered around apex

133
Q

Gingival Cyst of Adult

A

Soft tissue part of Lateral Periodontal Cyst

NO Radiolucency bc not in bone

134
Q

Gingival cyst of Newborn

A

Rests of dental lamina epithelialize the small lesions

Bohn’s Nodules=Lateral Palate
Epstein’s Pearls=midline palate

Tx: None,
* will go away as children get older

135
Q

Primordial Cyst

A

Develops where a tooth would have formed, but didn’t

Most common area=Mandibular 3rd molar

Tx: Complete removal

136
Q

Keratocystic Odontogenic Tumor (KCOT)

A

Aggressive & recurrent

Posterior Ascending Ramus of Mandible:
* Fusiform, M-D expansion (Not B-L)
* minimal displacement of teeth or resorption

Tx: Aggressive enucleation

137
Q

Gorlin Syndrome

A

=Multiple KCOTs (Keratocystic odontogenic tumor)

+ Multiple BCCs (Basal Cell Carcinomas)

+ Calcified Falx Cerebri

+ Fatal Disease

Aka Nevoid Basal Cell Carcinoma

138
Q

Calcifying Odontogenic Cyst

A

aka Gorlin Cyst

Rare & Unpredictable

Involves: Ghost Cells
* empty space and filled w/keratin–> Calcify
* Little radiodencities on x-ray

139
Q

Ameloblastoma

A

Benign BUT very AGGRESSIVE

Posterior Mandible
* Multilocular expansive lesion (Beach Ball B-L Expansion) w/erosion and displacement of roots & cortical bone

Tx: Wide excision or resection
* if too conservative=high recurrence

140
Q

Classic Differential Diagnosis for Multilocular Radiolucency in posterior mandible?

A

Ameloblastoma

KCOT (Keratocystic Odontogenic Tumor)

CGCG (Central Giant Cell Granuloma)

COF (Central Odontogenic Fibroma)

141
Q

Calcifying epithelial Odontogenic Tumor (CEOT)

A

Aka Pindborg Tumor

Radiolucency with driven snow calcifications (White flecks)

Liesegang rings: amorphous pink amyloid w/concentric calcifications

Tx: Surgical Excision, good prognosis

142
Q

Adenomatoid Odontogenic Tumor (AOT)

A

anterior maxilla over impacted canine (most common)

Contains:
* epithelial duct-like spaces
* enameloid material

143
Q

Odontogenic Myxoma

A

aka Myxofibroma

Myxomatous CT=Slimy stroma
* Pulp-like material w/minimal collagen

Messy radiolucency with:
* unclear borders
* honeycomb/tennis racket pattern

Tx: Surgical Excision, moderate recurrence

144
Q

Central Odontogenic Fibroma (COF)

A

Dense collagen w/strands of epithelium woven w/in it

Types:

Central:
* Bone
* well defined multilocular radiolucency

Peripheral:
* Gingiva
* No RL (not seen on x-ray)

145
Q

Cementoblastoma

A

Well-circumscribed radiopaque mass
* ball of cementum + cementoblasts= replace root of tooth

Connected to the root (Surrounded by a PDL Space)

tx: Surgical excision and extraction

146
Q

Ameloblastic Fibroma

A

Children & Teens

Posterior mandible
* contain: Myxomatous CT

Tx: Surgical Excision

147
Q

Odontoma

A

Opaque lesion
* composed of dental hard tissues
* block eruption of teeth

2 types:
Compound:
* anterior
* “bag of teeth”

Complex:
* posteiror
* conglomerate mass of dental tissue

148
Q

Gardner Syndrome

A

=Multiple Odontomas
+ Intestinal Polyps

149
Q

Hodgkin’s Lymphoma

A

Oral cavity=rare

Reed-Sternberg cells= Malignant B cells

Tx: Chemo +/- radiation

150
Q

Non-Hodgkin’s Lymphoma

A

Neoplasm of B or T cells

Burkett’s Lymphoma= Type of B cell NHL
Involves:
* bone marrow
* swelling
* pain
* tooth mobility
* Lip paresthesia (Pins & needs)
* Halted tooth development

Tx: Chemo +/- chemo

151
Q

Multiple Myeloma

A

Aka Plasma Cell Myeloma

Neoplasm of Plasma Cells
* Antibody-secreting B cells

multiple punched out radiolucencies in skull

Amyloidosis
* Accumulation of amyloid proteins-from antibody light chains

Tx: Chemotherapy- Poor prognosis

152
Q

Leukemia

A

Neoplasm of Bone Marrow cells:
* Lymphocytes
* NK Cells
* Granulocytes
* Megakaryocytes

Classification based on cell lineage (Myeloid or lymphoid) & Acute vs chronic:
* ALL -> CML -> AML -> CLL (Youngest to oldest)
* ALL Children Are Chill

Clinical Signs:
* Bleeding (Platelets)
* Fatigue (RBC)
* Infection (WBC)

Even though we are seeing increased production of bone marrow cells, they are immature & have less fxn

153
Q

Central Giant Cell Granuloma (CGCG)

A

Anterior Mandible mostly

Composed of:
* Fibroblasts
* Multinucleated Giant cells

Types:
Central (CGCG):
* Bone
* RL w/thin wipsy septations

Peripheral:
* Soft tissue
* Red-purple gingival Mass

Tx: Excision

154
Q

Aneurysmal Bone Cyst

A

Pseudocyst w/ blood-filled spaces

Posterior Mandible
* Multilocular Radiolucency:
* Expansile

Tx: Fine Needle Aspiration 1st (Blood=Confirms Dx)
* Excision

155
Q

Hyperparathyroidism

A

Multiple bone lesions that look like CGCG’s
* due to Excessive PTH Levels

Brown Tumor:
* Excess osteoclast activity–> Elevated Alkaline Phosphate

156
Q

Cherubism

A

Clinical: Symmetrical Bilateral Swelling

Radiographically:
* expansile bilateral multilocular RL

Stops growing after puberty

157
Q

Langerhans Cell Disease

A

Aka Idiopathic Histiocytosis
Rare Cancer

Langerhan cells (Histiocytes):
* normally found in skin as antigen-presenting cells
* Cause damage if buildup in body

Punched out “Ice cream scoop” radiolucencies
* lead to floating teeth

158
Q

Paget’s Disease

A

Progressive Metabolic Disturbance of many bones (Spine, femur, skull, jaws)
* Causes symmetric enlargement

Cotton Wool Appearance

Adults > 50
* Increased Bone Breakdown=Elevated alkaline phosphate
* Denture & hats become too tight

Associated with: hypercementosis

Tx: Bisphosphonates & Calcitonin

159
Q

Central Ossifying Fibroma

A

Fibroblastic Stroma: form foci of mineralized products
* Similar in appearance & Behaviour to cementifying fibroma (Odontogenic tumor)

3 types:
Central:
* Bone
* Well circumscribed RL w/ossificaotin product in center

Peripheral:
* Soft tissue
* no RL

Juvenile:
* Aggressive variant
* rapid growth
* younger pts

160
Q

Fibrous Dysplasia

A

Ground Glass Appearance
* Fiberglass–> Fibrous Glass

Stops growing after puberty

Tx: Surgical recontouring for cosmetics (after puberty)

161
Q

Periapical Cemento-Osseous Dysplasia (PCOD)

A

Reactive Process
* Unknown Origin

Most common:
* apices of mandibular anteriors
* Middled aged black females
* Vital Teeth

Starts RL–>progress to RO (w/RL halo) as it matures

162
Q

Osteoblastoma

A

Circumscribed opaque mass of bone & Osteoblasts

163
Q

Acute Osteomyelitis

A

Cause:
* Odontogenic Infection
* Trauma

Infection/inflammation:
* Starts in the medullary space involving cancellous bone
* spreads to cortical bone, periosteum, soft tissues

Symptoms:
* Deep intense pain
* high or intermittent fever
* Paresthesia or anesthesia of IAN
* Tooth is not loose (This is caused by periodontitis)

Tx: Antibiotics

164
Q

Cardinal Signs of Systemic Infection

A

FML!

Fever
Malaise
Lymphadenopathy

165
Q

Chronic Osteomyelitis

A

Diffuse Mottled Radiolucency

Garre’s Osteomyelitis:
* Chronic Osteomyelitis w/proliferative periosteitis (onion skin)

Tx: ANtibiotics & debridement of infected area

166
Q

Focal Sclerosing Osteomyelitis

A

Aka Condensing Osteitis

Bone sclerosis
*resulting from low-grade inflammation (like chronic pulpitis)

Tx: None, address cause of inflammation

167
Q

Diffuse Sclerosing Osteomyelitis

A

Same as Focal, BUT wider scale
* may lead to Jaw fracture

Bone Sclerosis:
* resulting from low-grade inflammation (like chronic pulpitis)

168
Q

What are the most common symptoms associated with Malignant bone lesions?

A

Nump lip/paresthesia

169
Q

Osteosarcoma

A

Sarcoma of the jaw
* new bone is produced by tumor cells

Sunburst Pattern of radiopacity

Tx: Resection & Chemo

170
Q

Bisphosphonate Related Osteonecrosis of the Jaws (BRONJ)

A

Greater risk w/IV Bisphosphonates than oral

5 yr survival rate: 25-40% (Pretty deadly)

Jaw Pain
* exposed necrotic bone

Tx: CHX rinse, antibiotics, conservative sx

171
Q

Chondrosarcoma

A

Sarcoma of the jaws
* New CARTILAGE is produced by tumor cells
* Same presentation & Tx as osteosarcoma

COndyle
*. Due to cartilage origin

172
Q

Ewing’s Sarcoma

A

Sarcoma of Long bones involving “Round cells”

Children
* rarely affects the jaw
* swelling

Moth Eaten or Onion skinning

173
Q

Metastatic Carcinoma

A

Breast > Lung > Kidney > Kidney > Prostate

174
Q

White Sponge Nevus

A

Asymptomatic spongy white lesion on buccal mucosa
* Doesn’t wipe off
* Autosomal Dominant

175
Q

Epidermolysis Bullosa

A

Skin & mucosa is fragile & Blisters easily
* Widespread blisteriing

176
Q

Hereditary Hemorrhagic Telangiectasia (HHT)

A

AkA Olser-Weber-Rendu Syndrome

Abnormal Capillary Formation on skin, mucosa, and viscera

associated with:
* iron deficiency anemia
* Espistaxis (Nose bleeds)=frequent sign

Telangiectasia=red macule or papule from diluted or broken capillaries

177
Q

Cleidocranial Dysplasia

A

Autosomal Dominant

Common Sign:
* Missing/poorly developed clavicles–shoulders appear hunched in towards midline
* Supernumery teeth

Tx: Alot of Extractoins & Dentures

178
Q

Ectodermal Dysplasia

A

X-Linked Recessive

Common Signs:
* Missing Teeth
* Hypoplastic hair or nails

179
Q

Amelogenesis Imperfecta

A

Intrinsic alteration of the ENAMEL in primary and permanent teeth
* Normal Dentin and Pulp

Autosomal Dominant, Recessive, or X-linked

Tx: Full coverage crowns for cosmetics

180
Q

Dentinogenesis Imperfecta

A

Intrinsic alteration of DENTIN in primary & permanent teeth

Autosomal Dominant

Characteristics:
* SHOrt roots, bell shaped crowns, & obliterated pulps
* Bulbous crowns in radiographs (Bc constricted DEJ)
* Blue sclera

Tx: Full Coverage crowns

181
Q

Regional Odontodysplasia

A

Quadrant of teeth exhibiting:
* short roots
* open apices
* enlarged pulp chambers

Radiographic:
* Ghost teeth: pulps are so huge they make the teeth look almost completely RL

Tx: Ext affected teeth

182
Q

Dentin Dysplasia

A

Intrinsic alteration of dentin in permanent & primary teeth

Autosomal Dominant

2 types:
* Type 1: Chevron Pulp w/short roots
* Type 2: Thistle shaped Pulp w/normal roots; Primary teeth=blue or amber color

Tx: Not good candidates for restorations

183
Q

Fusion & Gemination

A

Fusion:
* 2 tooth buds merging into 1 tooth
* Tooth count=1 less than normal

Gemination:
* 1 root buds into 2 crowns
* tooth count=normal