Vesicular, Bullous and Erosive Lesions l Oral medicine MCQ (multiple choice question) for dental students
Oral ulcers
Reactive ulcers :
- in infants are called Riga Fede Disease
- Ulcers with very well defined borders → indicate a specific
disease
- Ulcers with irregular border → trauma
- Usual sites for trauma = buccal mucosa , lateral
border of the tongue
- The
most important thing in traumatic ulcers = establishing a cause and effect
relationship
Chronic
ulcers :
- indurated + pain is disproportionate compared to the appearance of the lesion
- Three examples:
- Factitious ulcers [ self inflicted ulcers] – appear in accessible areas , have abnormal appearance and mostly linked to psycological disturbances
- Traumatic Eosinophilic Ulcer : significant eosinophilic presence
- Necrotizing Sialometaplasia
Necrotizing sialometaplasia:
- Cause:
vasoconstriction
induced by LA → ischemia and necrosis [
iatrogenic cause]
- M/S=
Squamous
metaplasia of ductal epithelium + Pseudo-epitheliomatous hyperplasia + necrosis
of salivary glands
- Treatment:
Reassurance,
mouthwash and observation of healing
- The complication that is most limiting to the continuation of chemotherapy is mucositis
N.B :
- Viral diseases will cause Vesicles / bullae that rupture to form an ulcer but bacterial or fungal infections cause ulcers right away!
BACTERIAL INFECTIONS CAUSING ULCERS
Syphilis
- Caused by treponema pallidum
- Route = sexually, by blood transfusion or trans-placental
- Three stages; deep ulcers are seen in the primary stage (chancre)
- You can see oral manifestations of shyphilis in all 3 stages :
- Primary stage [ chancre – deep indurated painless ulcers]
- Secondary stage [ condyloma latum ]
- Tertiary stage [ gumma]
- Dx: Darkfield examination of exudate + Silver stain
- Treatment : penicillin
Gonorrhea
- caused by nissesira gonorrhea - route : sexual contact – Tx: penicillin
Tuberculosis
- Caused by acid-fast aerobic bacillus Mycobacterium [ has fungal and bacterial features]
- Route = airborne
- Bacteria are not degraded by macrophages because
of their thick waxy coat → macrophages
aggregate to form multinucleated giant cells and granulomas result
- [ the granuloma forms because the body cannot digest the TB]
- Oral TB infections [ chronic , indurated , non healing ulcers] are secondary to lung infections through seeding by sputum [ the infection is in the lungs but when the pt coughs the infected sputum will go to the mouth causing the oral ulcers]
- In TB the bacteria is not harmful [ because it is contained in the granuloma ]
- MS=
- Granulomatous inflammation with caseous necrosis [ a granuloma is a tissue that forms to prevents the further spread of bacteria , it is not a place where cells live it is where cells die]
- Langhans multinucleated giant cells
- Presence of acid-fast bacilli (detected by ZiehlNeelsen stain or Fite stain)
- Treamtent: Strong antibiotics and chemotherapeutic agents
FUNGAL INFECTIONS CAUSING ULCERS
Deep fungal infections
- Fungi inhaled → pulmonary disease → oral
ulcers (seeding by infected sputum) - chronic , indurated , non healing
ulcers
- Deep fungal infections :
- Histoplasmosis – Coccidioidomycosis- Blastomycosis – Cryptococcosis
- MS=
- Pseudo-epitheliomatous hyperplasia
- Granulomatous inflammation
- Sometimes with abscess (blastomycosis)
- Treatment: amphotericin B or Azoles [
antifungals]
Oppurtonistic fungal infections
- phycomycosis (mucormycosis) and Aspergillosis
- route = GIT or pulmonary
- Affects medically-compromised patients
- Cause
necrosis and ulceration of the tissues and can perforate palate,
nasal cavity and orbit, and extends to the brain → Death
- Treatment: amphotericin B + surgical
debridement
IMMUNE MEDIATED ULCERS
Recurrnet aphthous ulcers [RAS] / canker sores :
- seen in higher socio-economic class, and in more developed countries
- causes:
- Genetic
- Haematological deficiency [ Iron (Fe-deficiency anaemia) , B12 (pernicious anaemia) , Folic acid (folic acid anaemia) ]
- Cyclic neutropenia
- GIT disorders [Coeliac disease , Crohn’s disease , Ulcerative colitis, H. pylori ]
- Hormonal changes [Relation to drop in progesterone ]
- Food allergies
- Stress
Other disorders with similar RAS presentation :
- Behçet disease (oral, genital ulcers, eye lesions and skin papulopustular lesions)
- HIV-related ulcers
- PFAPA (Periodic Fever, Aphthus, Pharyngitis, Adenitis)
- Sweet syndrome (oral ulcers, conjunctivitis and inflamed skin nodules)
NOTE:
- Per-ulcerative RAS lesions have CD4+ cells - Ulcerative lesions
have CD8+ cells (cytotoxic)
RAS is diagnosed when other diseases with oral ulcers are excluded
- Recurrent aphthous ulcers [ Floor is white (CT) then turns yellow (Fibrin) then turns grey (granulation tissue) ] + Surrounded by an erythematous halo ]
minor
- Small round to oval ulcers
- Seen mainly on non-keratinized mucosae
- Heals in about 1 week without a scar
- Painful
Major
- Large round to oval ulcers (around 1cm in diameter)
- Seen on any mucosal surface
- Heals in about 10-40 days - Might leave a scar
- Can be painful
Herpetiform
- Multiple minute pinhead ulcers which coalesce into large ragged ulcers
- Seen on any mucosal surface
- Heals in at least 10 days
- Recurs very frequently, almost continuous oral ulceration
- extremely painful
Treatment:
- R/o systemic cause
- Encourage high standards of oral hygiene [ pain is caused by the secondary bacterial infection on the ulcers , by maintaining oral hygiene you reduce the pain and accelerate the healing]
- Topical corticosteroids / Intra-lesion injection of corticosteroids
- Immune suppressants
Behçet’s syndrome
- seen in countries around the Silk Road (Middle East to Japan).
- Mostly males - oral, genital ulcers, eye lesions and skin papulopustular lesions
- Cause = vasculitis related to immunecomplexes affecting the involved tissues
- Strong link with and HLA-B51 [ used for screening]
- Ulcers are similar to minor RAS but they are larger , located in posterior mouth, and show more ragged edges.
- Dx of behcet’s syndrome:
- RAS, plus two of the
following
- Recurrent genital ulceration
- Eye lesions (posterior uveitis)
- Skin lesions (erythema nodosum, acneiform nodules)
Positive pathergy test :
- pricking the skin with a sterile needle and look for erythema or papule formation .
N.B :
- Bechet’s disease is a leading cause of blindness in young males, and might result in death from CNS or CVS complications.
Erythema multiforme:
- Allergic reaction [ acute, or even explosive onset] affects the mouth and the
skin
- Ranges in clinical symptoms → that’s
why it’s called multiforme
Three types:
- Minor EM, Major EM (SJS) and Toxic Epidermal Necrolysis (TEN).
- Affects anterior mouth – non keratinized tissue
- Lips are cracked, crusted and edematous + blisters and ulcers + skin has target lesions [ iris lesions]
- Minor form → affects one site, and is
less severe (self-limited).
- Major form [
steven jhonson’s syndrome] → oral
mucosa (severe pain, lip crusting) + Preceded by a prodromal flu-like
symptoms + Involvement of [pharynx, eyes , genitals , Symmetrical
involvement of skin]
Cause:
- Abnormal reaction to microorganisms or drugs [
most cases] leading to immune complexes depositing in the superficial Blood vessels of
skin and mucosa [ vasculitis] → necrosis
Treatment:
- Supportive therapy + referral to ophthalmology and dermatology
- If viral induced → give
acyclovir
- If drug induced → give
corticosteroids [ don’t give corticosteroids if it is cause dby infection]
- Plasmapheresis
Q: plasma cell infiltrate ins seen in ?
- contact allergy
Q: valsculitis is seen in ?
- behcet’s syndrome and erythema multiforme
Q: stevenes jhonson’s syndrome is ?
- major EM
Q: target lesions are seen in ?
- Erythema multiform
Orofacial granulomatous diseases
- Mainly seen involving the upper lip, then lower lip, then cheeks.
- Should R/O:
- Crohn’s disease
- Sarcoidosis [ mostly affects lymphoid tissue]
- Foreign body reaction
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