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Granulomatous Diseases of the Skin

»What is meant by “granulomatous diseases of the skin”?
»Explain the role of histiocytes in granulomas.
»What is the difference between an immune granuloma and a foreign body granuloma?
»List some common granulomatous diseases that affect the skin.
»Can granulomas be recognized clinically?
»How do endogenous “foreign” bodies cause granulomas?
»What are the sources of the exogenous foreign body agents?
»Do cosmetic fillers ever produce foreign body granulomas?
»Can the cause of a foreign body reaction be diagnosed histologically?
»What is sarcoidosis?
»How often is the skin involved in sarcoidosis?
»Describe the specific cutaneous findings in sarcoidosis.
»What is lupus pernio?
»Describe the nonspecific cutaneous lesions of sarcoidosis.
»Does sarcoidosis ever present in the skin without extracutaneous involvement?
»What is Löfgren’s syndrome?
»What is Heerfordt’s syndrome?
»How should cutaneous sarcoidosis be treated?
»What is the typical presentation of granuloma annulare?
»Do any systemic associations occur with granuloma annulare?
»What is the typical course of granuloma annulare?
»How is granuloma annulare treated?
»What is actinic granuloma?
»Are rheumatoid nodules really a granulomatous disorder?
»Where do rheumatoid nodules typically occur?
»What causes rheumatoid nodules?
»What is accelerated nodulosis?
»Are rheumatoid nodules specific for rheumatoid arthritis?
»Do patients with lupus miliaris disseminatus faciei have lupus erythematosus?

 
 
 

What causes rheumatoid nodules?

The pathogenesis is not understood, but the evidence suggests that rheumatoid arthritis occurs in genetically susceptible patients after an arthritogenic microbial antigen exposure. The identity of the microbial trigger has not been established, although considerable attention has been placed on the Epstein-Barr virus. Once the process is initiated, a complex autoimmune disease develops characterized by increased numbers of CD41 T cells in the joint, which also activate B cells that produce autoantibodies (primarily IgM) to the Fc portion of autologous IgG. The antigen that provokes the autoimmune response has not been fully established, but research is focusing on type 2 collagen, human cartilage glycoprotein-39, human stress protein BiP, and several different heat shock proteins. How this autoimmune response produces rheumatoid nodules is not clear.


Bodman-Smith MD, Corrigall VM, Berglin E, et al: Antibody response to the human stress protein BiP in rheumatoid arthritis, Rheumatology (Oxford) 43:1283–1287, 2004.

Sawada S, Takei M: Epstein-Barr virus etiology in rheumatoid synovitis, Autoimmune Rev 4:106–110, 2005.