ORAL PATHOLOGY Flashcards
Which teeth are most commonly affected by taurodontism?
A) Wisdom teeth
B) First molar
C) Second molar
D) Premolars
A)
WT > Second molar > First molar
Which three teeth are most commonly affected by internal root resorption?
1, 6 and 7s
Which of the following pathologies are commonly associated with the anterior maxilla region and dental abscesses?
A) Taurodontism
B) Dental dysplasia
C) Regional odontodysplasia
D) Dens evaginatus
C)
Distinguish the two types of dentinal dysplasia
Type 1 - Radicular
- pA radiolucency
- Pulp obliterated
- Unremarkable clinical appearance
Type 2 - Coronal
- Primary dentition only
- Opalescent apperance
- Thistle tubed pulp space
- May have pulp stones
Briefly distinguish the clinical features of acute periapical periodontitis vs chronic periapical periodontitis.
APP:
- Constant severe tooth ache
- Hypersensitivity to testing and TTP
- Tooth elevated in socket
- Swelling
CPP:
- Asymptomatic
- Occasional dull ache
- Minimal to no response to testing
A patient presents to your clinic with an asymptomatic bony, hard swelling. Histology: Osteoclast and osteoblasts, marrow spaces filled with fibrous tissue and lymphocytes
Radiology: Irregular, predominantly radiolucent lesion, expansion of PDL with concentric/parallel opaque layers (onion skin)
Which of the following is most likely?
A) Fibrous dysplasia
B) Tori
C) Acute suppurative osteomyelitis
D) Garre’s osteomyelities
D)
Explain the radiographic appearance of a dentigerous cyst.
Development cyst
- Attached to CEJ and covering crown
- Well-defined round corticated radiolucency
- > 3mm (requirement to dx from normal follicle)
Can become very large - Unilocular
- Displaces/resorbs adjacent teeth and structures
Explain clinical feature of dermoid/epidermoid cysts - where are they commonly found? Distinguish the two based on histology.
Slowly growing doughy cysts - usually <2cm
Dermoid
- Stratified squamous epithelium
- Keratinised debris
- Hair follicles, sebaceous glands and sweat glands
Epidermoid
- Stratified squamous epithelium
- Keratinised debris
In relation to pyogenic granuloma:
- Aetiology?
- Three common places to appear?
- Clinical appearance?
- Histology?
- Aetiology: response to local irritation or trauma
- Common: Gingiva, lips, tongue
- Clinical: red mass, may be ulcerated, lobulated, spongy feeling
- Histology: Granulation tissue - highly vascular
A 13 year old patient presents to your clinical with a bilateral swelling of the cheeks. On radiographic examination, you note a multilocular, soap-bubble radiolucency. Histological examination indicates large amounts of multinucleated osteoclast-like giant cells in a vascular fibrous tissue. Which is the most likely diagnosis?
(A) Fibrous dysplasia
(B) Cherubism
(C) Central giant cell granuloma
(D) Ameloblastoma
(B) Factors that indicate this is most likely diagnosis:
- Young age
- Bilateral involvement
- Histology and radiographic examination match
A 24 year old male presents to your clinic with a brown-black pigmented lesion on the buccal gingiva region of tooth 46. Radiographic examination is unremarkable and histological examination indicates an increase in melanin pigment in basal layer. Which of the following is the most likely diagnosis?
(A) Amalgam tatoo
(B) Acquired melanocytic naevus
(C) Melanotic macule
(D) Melanoma
(C)
Briefly explain the histology of true oral lichen planus.
o Band-like lympho-histiocytic infiltrate in lamina propria – hugging overlying surface epithelium
o Varying degrees of ortho/parakeratosis
o Rete ridges may be atrophic or hyperplastic – classically described as saw-toothed
o Destruction of basal keratinocytes – hydropic degeneration – NO DYSPLASIA
o Necrotic keratinocytes – civatte / colloid bodies
o NO PLASMA cells
o Superadded Candida infection
What are the three common drugs that cause drug-induced gingiva hyperplasia?
- Phenytoin (anticonvulsant)
- Cyclosporine
- CCB - Nifedipine, verapamil
Explain the following in relation to peripheral ossifiying fibroma.
- Clinical appearance
- Histology
- Clinical: same appearance as normal mucosa (unless ulcerated), sessile or pedunculated, growth is NOT self-limited, usually <2cm in size
- Histology: Proliferation of fibroblasts, calcified deposits of bone, cementum-like material and dystrophic calcifications
Distinguish junctional, compound and intradermal acquired melanocytic naevus.
Lesion becomes increasingly raised and pale in appearance the deeper the naevus cells are located → Evolve lifetime from junctional to deeper regions
Junctional:
Well circumscribed brown-black macule
Compound:
Central raised area with surrounding flat pigmentation
Brown-tan
Intradermal:
Elevated/dome shaped
Pale
Distinguish the histology between acquired melanocytic naevus, melanotic macule (ephelis), and melanoma
Acquired melanocytic naevus: Cluster of naevus cells in the wrong location (normal in appearance)
Melanotic macule: Size, number and appearance of melanocytes are normal but increase melanin production
Melanoma: Pleomorphic - increased number and atypical appearance of melanocytes
Merkel cells are located in:
(A) Prickle layer of masticatory mucosa
(B) Basal layer of masticatory mucosa
(C) Prickle layer of lining mucosa
(D) Basal layer of lining mucosa
B)
Under a histological slide, you note the following:
- Large flat keratinocytes
- Keratohyalin granules
- Odland bodies dishcarging extracellular contents
Which of the following is this layer of the mucosa most likely to be?
(A) Basal layer
(B) Prickle layer
(C) Granular layer
(D) Keratinised layer
(C)
On radiographic examination in an 8 year old patient. You notice that in general, the dentition appears to:
- Have short roots
- Pulpal obliteration
- Radiolucency of the dentine
What would your list of ddx be based on the information above? (List characteristic signs for each that would help narrow down the ddx if further info was provided)
- Dentinogenesis imperfecta –> Bulbous crowns, exaggerated CEJ, amber/opalescent appearance of teeth
- Dentinal dysplasia
> Type 1 Radicular: clinically unremarkable, pA radiolucencies
> Type 2 Coronal: primary teeth only, pulpal stones may be present, amber/opalescent appearance –> UNLIKELY as coronal pulp is large and canals described as thistle shaped rather than obliterated - X-linked Hypophosphataemia (Vit D resistant rickets): pulp horns enlarged to DEJ, enamel hypoplasia
List three ddx for condensing osteitis and note where possible, distinguishing features that can ascertain the definitive diagnosis
Diffuse sclerosing osteomyelitis: chronic form of OM with pronounced sclerotic response
Fibrous scarring post RCT
Late periapical osseous dysplasia → Vital teeth and nil history of pain/pulpal infection, radiolucent rim around radiopacity
Cementoblastoma → Spokes of wheel appearance with radiolucent rim just inside the corticated border
Dense bony islands → Nil history of pain/pulpal infection, radiopacity is less symmetrical and not as centred/attached to root apex
List radiographic and clinical ddx for radicular cyst and note where possible, distinguishing features that can ascertain definitive diagnosis.
Radiographic:
- Chronic apical periodontitis → Ill-defined borders that blend into the bone and <1cm
- Early cemento-osseous dysplasia → Teeth remain vital and become radiopaque/mixed upon maturation
- Radiolucent apical scar
- OKC
- Lateral periodontal cyst
- Central giant cell granuloma → Vital teeth and clinically present as a swelling
Clinically - Red/blue swelling:
- Pyogenic granuloma → Removal of irritant will resolve lesion and minimal to nil radiographic evidence
- Periapical giant cell granuloma → Minimal to nil radiographic evidence
List radiographic and clinical ddx for dentigerous cyst and note where possible, distinguishing features that can ascertain definitive diagnosis.
Paradental/BBC → Covers coronal ½ of root and epicentre at buccal bifurcation
Pericoronitis → WT is partially erupted
OKC → Does not expand bone to same degree, lack of resorption and often attaches further apically on root rather than CEJ
Unicystic ameloblastoma → Difficult to distinguish
Ameloblastic Fibroma
Rare
Adenomatoid odontogenic tumour
Calcifying odontogenic cyst
List clinical features/patient complaints in relation to xerostomia and salivary hypofunction
1.Xerostomia
Dry mouth
Difficulty masticating and swallowing
Speech affected
Taste disturbance
Sleep disturbance
2.Salivary hypofunction
Minimal pooling in FoM
Stringy/frothy saliva
Mirror sticking to mucosa
Fissured and depapillated tongue
Atypical caries
Candidiasis
What are the four pillars of managing a patient with salivary hypofunction?
- Symptomatic relief –> Biotene, Oral 7 or GC Dry mouth (note: biotene and oral 7 spray are identical) - no brand or type is more superior than the other. Advise patient reapplication required
- Caries control
- Regular recalls
- Dietary advice and OHI
- Home fluoride regime - Sialagogues
- Gustatory
- Masticatory (e.g. sugar free gum
- Pharmacology = Pilocarpine
> Contraindicated in narrow angle glaucoma
> Relative contraindication in asthma and cardiac patients
> Need good residual functioning tissue - Disease modifying agents –> Beyond scope of dentist