Pemphigus vulgaris

• Type: Autoimmune blistering disorder 

• Autoantibodies: Against Desmoglein-3 (mucosa) ± Desmoglein-1 (skin) — components of desmosomes 
• Hypersensitivity type: Type 3 Hypersensitivity (Ag-Ab complex)

• Blister type- Flaccid, Intraepidermal blisters 

 

Pemphigus group

of disorders 

Pemphigoid group

of disorders

Bullae 

Flaccid bullae

Tense bullae

(because whole epidermis 

is present in bulla covering 

so bulla is tight / tense)

Bullae 

Location

Intra epidermal

Sub epidermal

Age of onset

40-60 year

60-80 year

(old age)

• Row of 

tombstone 

• Acanthocytes 

• Nikolsky sign

• Mucosal

involvement

• Intra epidermal

bullae

Present 

Absent

Bulla spread sign 

Present 

Present 

Mucosal involvement: 
• Always present, commonly starts in the oral cavity 

Skin Lesions: 
• Painful, flaccid bullae that rupture easily → erosions 

Nikolsky sign: 
• Positive (gentle pressure causes skin to shear off)

Acantholysis: 
• Seen on histology (loss of cohesion between keratinocytes) 

Histology: 
• Row of tombstones appearance (It refers to the appearance of basal keratinocytes that remain attached to the basement membrane after the upper layers of the epidermis split due to acantholysis)

Immunofluorescence:
• Intercellular IgG deposition in a “net-like” or “fishnet” pattern 

Treatment: 
• High-dose corticosteroids, immunosuppressants (azathioprine, rituximab) 

Pemphigus Vulgaris

 

Pemphigus Foliaceus

DSG 3 > DSG 1

Antigen

DSG1

Suprabasal

Split

Subcorneal

Always present 

Mucous memb

involvement

Absent 

Crusted erosions 

Vesicle & Bullae

On skin

Crusted erosions 

(Seborrheic distribution)

 

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