Vesiculobullous lesions 1 Flashcards

1
Q

What are the immune mediated diseases with local effects on the mouth?

A

Aphthous ulcers

LP

OFG

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2
Q

What are the systemic immune mediated diseases which can also appear in the mouth?

A

Erythema Multiforme
Pemphigus
Pemphigoid
Lupus erythematosis
Systemic Sclerosis
Sjogren’s Syndrome

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3
Q

What type of hypersensitivity reaction is associated with erythema multiforme?

A

Type 3- related to antigen-antibody complexes

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4
Q

What immunogenic oral diseases are cell mediated?

A

Aphthous ulcers

Lichen Planus

Orofacial Granulomatosis

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5
Q

What immunogenic oral diseases are antibody mediated?

A

Pemphigus

Pemphigoid

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6
Q

Why are skin and oral immunological diseases related?

A

Often affects both due to common embryological origin

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7
Q

What is the difference between an antigen and an epitope?

A

Antigens- big immunogenic sites within protein

Epitope is the small part in sequence of protein which antibody binds to

-> Binding at these can affect conformation of protein

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8
Q

How does antibody binding to different epitopes affect disease course in Epidermolysis Bullosa?

A

Depending on epitope it can be mild or lethal form

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9
Q

How does damage occur in immunological skin diseases?

A

Auto-antibody attack on skin components (hemi-/desmosomes) causing loss of cell-cell adhesion

‘Split’ forms in skin
-> Fills with inflammatory exudate (forces apart layers)
-> Forms vesicle/blister

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10
Q

Which protein is targeted within desmosomes in immunobullous diseases?

A

Desmoglein

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11
Q

What is the difference between a vesicle and a blister?

A

Vesicle- 1-2mm

Blister- larger

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12
Q

How does direct immunofluorescence used to identify antibodies causing immunological conditions?

A

Secondary antibody with fluorescein binds to the primary antibody which is bound in the tissue
-> can be seen under fluorescent light

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13
Q

What are the requirements for DIF?

A

Sample must not be put into formalin containing transport medium as it causes loss of binding sites

Must be transported fresh and processed quickly

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14
Q

When is indirect immunofluorescence used?

A

When identifying a circulating antibody which is not bound in tissue
-> done using plasma samples

Less reliable for diagnosis but good for monitoring disease

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15
Q

Which disease is indirect immunofluorescence useful for?

A

Pemphigus- as antibody levels direct treatment need

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16
Q

What is erythema multiforme?

A

Spectrum disorder of Immunogenic related skin and mucosa ulceration
-> Variable orofacial involvement

17
Q

What causes Erythema multiforme to occur?

A

 Antigen presents which is targeted by antibody (antigen is usually one that has been met before and prompt immune response follows- antibodies produced by memory B cells)

 Antigen and antibody combine to form complexes in circulation but cannot pass through capillaries, it can become wedged in tissue and results in activation of complement within BV causing perivascular inflammatory response (If significant- blistering and ulceration of tissue presents)

18
Q

How does EM present in skin and mucosa?

A

Skin- target lesion/crusting lesions

Mucosa- ulcers
-> present similar to primary herpetic gingivostomatitis (can affect keratinised tissue)

Lesions tend to last for 2-3 weeks, there may be months between episodes or they can develop very quickly

19
Q

What are the causes of EM?

A

Drugs

HSV reactivation triggering T3 rxn

Mycoplasma- infective agent

20
Q

What areas can EM affect?

A

Mouth

Skin

Eyes- conjuctivae

Genitals

If multi-system and severe- it is known as Steven Johnson Disease

21
Q

How is oral lesions in EM managed?

A

Drugs
-> systemic steroids – up to 60 mg/day (a high dose)
-> systemic aciclovir

Encourage fluid intake- May require admission for IV fluid if unable to drink due to discomfort

Encourage analgesia

22
Q

How is recurrent EM managed?

A

Consider prophylactic aciclovir daily

Allergy test – a wide variety of environmental triggers

23
Q

What is the dose of prophylactic aciclovir for EM?

A

400mg x 2 daily
-> helps supress virus replication and prevent emergence of EM and production of antibodies/immune complexes

24
Q

What is angina bullosa haemorrhagica?

A

Angina- tight, Bullosa- blister, haemorrhagic- blood filled
-> painless blood blisters which occur in the mouth

25
Q

What are the most common sites for ABH?

A

Buccal mucosa

Soft palate
-> sometimes occurs at junction of soft and hard palate and can feel like airway is closing

26
Q

What are the causes of ABH?

A

Minor trauma- can be from eating

Steroid inhalers

27
Q

How long do ABH lesions last?

A

Rapid onset- form within minutes

Burst within one hour
-> may leave mildly symptomatic ulcer

28
Q

What do healing ABH lesions look like?

A

Aphthous ulcers- to differentiate ask if the lesion was previously a blister

29
Q

What should patients be informed if they are worried about the colour of the liquid that comes out on bursting of ABH blister?

A

That it is fluid that is blood stained due to RBC presence within rather than any worrisome bleeding
-> not related to platelet/coagulation defect

30
Q

What does ABH come up as on histological testing?

A

Non-specific ulceration

  • also negative to DIF/IF testing
31
Q

What can be used to treat symptoms of ABH?

A

CHX mouthwash

Difflam mouthwash