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Description

A patient with systemic lupus erythematosus (SLE) may develop oral lesions.


Prevalence: 7-52%

 

Clinical presentations:

(1) mucosal ulceration, typically painless

(2) discoid lesions (central areas of erythema with white spots surrounded by radiating white striae and telangiectasia

(3) erythematous lesions

(4) hyperkeratotic lesions

 

Histopathologic features:

(1) interface mucositis

(2) hyperkeratosis with keratotic plugging

(3) liquefactive degeneration

(4) perivascular inflammation, usually lymphohistiocytic

(5) intra-epithelial microabscesses

(6) spongiosis

(7) civatte bodies (colloid bodies)

(8) multi-nucleated epithelial cells

 

Immunohistological findings:

(1) deposits of IgM and IgG along the dermal-epidermal junction

(2) deposits of complement along the dermal-epidermal junction

(3) deposits of fibrinogen along the dermal-epidermal junction

 

Differential diagnosis:

(1) lichen planus

(2) leukoplakia

(3) infection

(4) drug adverse effects


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