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Postgraduate Medical Journal 2000;76:457-465; doi:10.1136/pmj.76.898.457
Copyright © 2000 The Fellowship of Postgraduate Medicine.
Postgrad Med J 2000;76:457-465 ( August )

Review

A clinicopathological classification of granulomatous disorders D Geraint James

Royal Free Hospital School of Medicine, University of London, Rowland Hill Street, London NW3 2PF, UK

Correspondence to: Professor James

Submitted 7 July 1999; Accepted 22 November 1999

Granulomatous disorders comprise a large family sharing the histological denominator of granuloma formation. A granuloma is a focal compact collection of inflammatory cells, mononuclear cells predominating, usually as a result of the persistence of a non-degradable product and of active cell mediated hypersensitivity. There is a complex interplay between invading organism or prolonged antigenaemia, macrophage activity, a Th1 cell response, B cell overactivity and a vast array of biological mediators. Differential diagnosis and management demand a skilful interpretation of clinical findings and pathological evidence. They are classified into infections, vasculitis, immunological aberration, leucocyte oxidase deficiency, hypersensitivity, chemicals, and neoplasia.


Keywords: granuloma; Th1 cell; cytokines; neoplasia


© 2000 by The Fellowship of Postgraduate Medicine

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