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Gougerot–Blum syndrome is a variant of Pigmented purpuric dermatitis, a skin condition characterized by minute, rust-colored to violaceous, lichenoid papules that tend to fuse into plaques of various hues.[1]:829 Relative to other variants, it is characterized clinically by a male predominance, puritis, with a predilication for the legs, and histologically, it features a densely cellular lichenoid infiltrate.[2]

[edit] See also

[edit] References

  1. ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0. 
  2. ^ Barnhill RL and Crowson AN (eds) Textbook of Dermatopathology, second edition, McGraw-Hill, 2004: 211-212



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