Description

A patient with primary or secondary syphilis may present with lymphadenopathy. The diagnosis can be challenging if the patient is not known to have syphilis.


 

Syphilitic lymphadenopathy may be localized or generalized.

 

Histologic features:

(1) follicular hyperplasia

(2) interfollicular plasmacytosis

(3) capsular and trabecular fibrosis with a plasma cell infiltrate

(4) variable endarteritis or venulitis with plasma cells

 

Less common findings may include:

(1) clusters of epithioid histiocytes

(2) sarcoid-like granulomas

(3) suppurative granulomas

(4) necrotizing lymphadenitis

 

Diagnosis is supported by:

(1) a positive serology test

(2) spirochetes visualized on silver or immunohistochemical stains

 

Differential diagnosis:

(1) rheumatoid arthritis or other autoimmune disorder

(2) malignant lymphoma

(3) other conditions associated with follicular hyperplasia

 


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