Vesiculobullous Lesions 2 Flashcards

1
Q

What is bullous lichen planus?

A

Condition with many of the features of pemphigoid superimposed on lichenoid histological pattern

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2
Q

What is pemphigoid?

A

Sub epithelial antibody attack resulting in persistent thick walled blisters (can be clear or blood filled)

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3
Q

How does damage to epithelium occur in pemphigoid?

A

Antibodies cause separation of epithelium from connective tissue at basement membrane by targeting hemi-desmosomes
-> full thickness of epithelium is released with fluid and inflammatory exudate filling space

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4
Q

Where does the fluid in pemphigoid blisters come from?

A

Fluid comes from connective tissue

As a result of immunological damage- RBCs may go into fluid giving it blood filled appearance

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5
Q

What are the types of pemphigoid?

A

Bullous Pemphigoid - skin

Mucous Membrane Pemphigoid – all mucous membranes affected (eye, genital, oral)

Cicatritial Pemphigoid – subset of mucous membrane- presence of scarring (different epitopes on same antigen involved in generation of lesion)

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6
Q

How should a biopsy of pemphigoid be carried out?

A

Take from peri-lesional tissue to aid diagnosis
-> as it is impossible to guarantee that epithelium will remain attached to underlying mucosa (characteristic features should still be seen)

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7
Q

How does pemphigoid appear histologically?

A

Split at junction of epithelial and connective tissue due to damage of heme-desmosomes at BM

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8
Q

How is pemphigoid tested for?

A

 DIF is best- immunofluorescent staining can be seen along BM (Linear basement membrane staining)
-> fluorescein tag is attached to antibody which binds to circulating pemphigoid antibody which binds to antigen in BM

 Antibody to which stain is bound can be c3 (usually always involved), IgG, IgM and IgA
-> Disease may behave differently depending on antibody triggering issue

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9
Q

How does staining appear in dermatitis herpetiformis appear?

A

Granular deposits of C3 and IgA seen
-> non linear like pemphigoid

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10
Q

What condition is DH associated with?

A

Coeliac

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11
Q

What can scarring of mucosa due to pemphigoid result in?

A

Narrowing of oro-pharynx (can be invisible)

Symblepharon- scarring of conjunctiva can bind eye surface to eyelid (restricts eye movement- dipoplia)
-> checked regularly by optician/ophthalmologist to see if this is developing

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12
Q

Which other healthcare professionals are involved in managing pemphigoid (esp circatritial)

A

 Ophthalmologist
 Dermatologist
 Oral physician

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13
Q

How is pemphigoid managed?

A

Immune suppressants to prevent antibody generation causing disease:

Steroids

IMD- azathioprine, mycophenolate, dapsone and biologics

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14
Q

How does damage in pemphigus occur?

A

Circulating antibody is formed against desmosome tissue which holds cells together (not hemidesmosomes)
-> these cells lose adhesion to each other as a result

Intraepithelial bullae form- there may only be a few layers of cells above or around lesion but fluid fills spaces causing drift (epithelium is initially thinned but is then completely lost)

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15
Q

What is the main difference between pemphigus and pemphigoid?

A

In pemphigus- intact bulla are rarely seen
-> presents as areas of surface loss and mucosal erosion

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16
Q

What areas are affected by pemphigus, what is the usual sequence?

A

Often presents orally first, can take up to 3 years for skin lesions to present
-> Skin also suffers from erosive loss of cell structure and widespread loss of epithelial covering (fluid loss and infection risk)

17
Q

Which groups are more likely to suffer from pemphigus?

A

Over 50s

Females

Ashkenazi jew population

18
Q

What are the histological features of pemphigus?

A

 Loss of epithelium and shedding of epithelial layer

 Supra-basal (split occurs above basement membrane)

 Tzank cells are characteristic

19
Q

What gives the basket weave appearance when immunofluorescence of pemphigoid is carried out?

A

Antibody attacks desmosomes which are present on many surfaces of epithelial cells giving immunofluorescent surrounding
-> different from linear BM staining in pemphigoid

20
Q

What is the commonest form of pemphigus?

A

Vulgaris

21
Q

Which antibodies are commonly identified in pemphigus vulgaris?

A

C3 and IgG

22
Q

How does pemphigus present clinically?

A

 Erosions rather than blisters (same in skin and mouth)
-> Intact bullae are rare- thin walled intra-epithelial blisters

 Can affect any part of oral mucosa

 Appears like desquamative gingivitis in mouth- loss of epithelial covering OR as area covered with fibrinous exudate

23
Q

How is pemphigus managed?

A

High dose of steroids, biologics and immunosuppressants are required to stop erosions and loss of epithelial coverage

-> Biologics are preferred as other medicines put patient at risk of other diseases

24
Q

Why must pemphigoid and pemphigus be managed by specialists?

A

They can be fatal