Soft tissue lesions Flashcards

1
Q

list developmental oral cyst of newborn
and management
(congenital)

A

Keratin: bohn nodules, epstein pearls, dental lamina cyst

blood: eruption cyst
management: clinical diagnosis and leave alone cept eruption cyst

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2
Q

location and origin of Bohn nodules

A

junction of hard and soft palate or on vestibular region (rare)
origin epithelial remnants of minor salivary glands

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3
Q

location and origin of epstein pearls

A

mid palate raphae

origin epithelium entrapment between palatal shelves

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4
Q

location and origin of dental lamina cysts

A

crest of alveolar ridge

odontogenic origin from cell rest of serres

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5
Q

appearance, location and origin of eruption cyst

A

soft, fluctuant sessile, dome shaped, translucent bluish colour
alveolar ridge
soft tissue variant of dentigerous cyst, from separation of reduced enamel epithelium from crown of tooth
treatment: naturally marsupializes as tooth erupts, symptomatic treatment of simple removal of roof of cyst (trauma and pressure causes discomfort)

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6
Q

what is ankyloglossia and effects

A

developmental: abnormally short anteriorly positioned lingual frenum that may result in restricted movement
effects: breast feeding difficulties, restriction of tongue movement
gingival recession in severe cases, speech and malocclusion

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7
Q

treatment for ankyloglossia

congenital

A

if breast feeding problems (<1month) frenotomy/frenolotomy (cut), frenectomy (tissue removed and more advanced surgical techniques)
internvene when: gingival stripping, recession, fremitus, tongue mobility with functional impairment (speech: sibilant sounds), diastema after perm canine eruption (mixed dentition)
poorly supported: malocclusion

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8
Q

vascular anomalities: tumours vs anomalities

congenital

A

tumours: endothelial proliferation (growth)
appears 1-3 months and high rate proliferates then involutes, F>M

malformations: structural problems, present at birth and only grows with child’s age, does not involute, (trauma, puberty, pregnancy can accelerate growth), no gender predilection

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9
Q

vascular tumour: infantile hemangioma

prevalence, characteristics and diagnosis and management

A

early infancy 1-3 months, F>M, predilection for head and neck region

clinical presentation: rapid growth and proliferation, benign, self limiting involution over time, may cause complications

management: depending on location
if in eyes/bone/tongue/brain/crucial areas will have compressive issues

different from congenital hemangioma clinically and histologically

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10
Q

vascular malformation classification and examples, syndromes

A

low flow: capillary, venous, lymphatic (lymphangioma)
high flow: ateriovenous malformation (arteries join to vein wo capillary, expansion of venous base)
combined
no gender predilection

sturge-weber (capillary)

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11
Q

lymphangioma
definition
prevalence
clinical presentation

A

def: bilated malformed lymphatic channels or cysts of varying size
prev: 50% at brith, 90% diagnosed by 2
pres: microcytic form, tongue most common, buccal mucosa second most, intraosseous (cystic hygromahard to take out)

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12
Q
congenital epulis
definition
prevalence
clinical presentation
histology
(congenital)
A

congenital granular cell tumour
pre: 0.0006% of newborns, 8-10 more common in females
pres: single, firm, smooth, sessile or pedunculated round mucosal coloured mass <2cm around anterior maxillary alveolar ridge
management: diagnosis clinical and histological
granular cell tumour with no display of strong reactivity to S100 protein
surgical excision, recurrence unlikely

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13
Q

primary herpetic gingivostomatitis

presentation and management

A
majority subclinical
incubation 5-7 days
prodrome 1-2 days
vesiculation and ulceration
symptoms reduce from 6th day
resolves in 10-14 days
around

mxn: symptoomatic care, anti-pyretic analgesic, fluids, 0.2% chlorhex, acyclovir within 72hr of infection for immunocompromised

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14
Q

reactivation of HSV

A

appears on keratinised tissue only: attached gingiva, vermillion border of lips

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15
Q

HPV types and management

A

6/11 most common
16/18 cause scc/cervical cancer
orals: squamous papilloma, verruca vulgaris, condyloma acuminatum (assoc sexual abuse), heck’s disease (Focal Epithelial Hyperplasia, is an asymptomatic, benign, precancerous? neoplastic condition characterized by multiple white to pinkish papules)
mxn: excisional biopsy except for heck disease

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16
Q

squamous papilloma vs verruca vulgaris

A

sp more keratinised, whiter

17
Q

superficial fungal inf in children and management

A

pseudomembranous candidiasis
angular cheilitis
median rhomboid glossitis
mxn: anti fungals: nystatin, clotrimazole
proper oral hygiene
wash utensils and store in antiseptic solution
identify underlying causes

18
Q

linea alba
prev
pres
mxn

A

<20s, no gender predilection
white smooth to shaggy line, bilateral coincides with place of occlusion
mxn: remove irritation if possible

19
Q

mucocele

A

<20s, no gender predilection

pres: lower labial mucosa, buccal mucosa, ventral tongue, localised, compressible, fluid filled nodule with smooth translucent to blue surface, fluctuate in size, may be tender, may be nodular if chronic
mxn: excisional biopsy

20
Q
recurrent apthae ulceration
prev
etio
pres
mxn
A

<20
F>M
etio: immune mediated, stress, trauma, allergies, nutrition, genetic
pres:
minor- 1-5 lesions, fewest recurrences, shortest duration
major- 1-10 lesions, longest duration, larger and deeper onset after puberty
herpetiform- most frequent recurrence, ~100 ulcers, F>M, onset in adulthood

21
Q

geographic tongue

A

benign chronic recurring inflammatory condition

many well demarcated areas of erythema red centre white border atrophic filiform papilla on dorsum of tongue

mxn: no treatment needed, avoid spicy food if its a trigger

22
Q

erythema multiforme
etio
pres
mxn

A

type III hypersensitivity

etio: immune mediated triggered by preceding infection of HSV/mycoplasma pneumonia, drugs
pres: blistering ulcerative mucocutaneous condition, acute onset prodromal common 1 weeks before onset, 2-6 weeks self limiting, recurrent in 20% of patients, oral lesions start as erythematous patch, large shallow erosions and ulcerations with irregular borders
mxn: steroids + antiviral prophylaxis (if people get it multiple times a year)

23
Q

4Ps of lumps and bumbs

A

pyogenic granuloma, peripheral giant cell fibroma, peripheral ossifying fibroma (calcification), peripheral fibroma

24
Q

gingival enlargement
reactive
developmental
systemic

A

drugs: cyclosporin, calcium channel blocker, phenytoin

25
Q
melanotic neuroectodermal tumor of infancy
etio
prev
pres
mxn
A

prev: rare, children <1 year
etio: neural crest origin

pres: painless, non-ulcerative, firm, smooth, sessile swelling on anterior maxillary alveolar ridge

benign (1% malignant) but rapidly growing and infiltrate and destruct adjacent structures

mxn: diagnosed through clinical pres, high urinary vanillylmandelic acid, histology
surgery intervention, recurrence 10-60%