Gougerot–Blum syndrome

Gougerot–Blum syndrome

Gougerot–Blum syndrome (also known as "pigmented purpuric lichenoid dermatitis",[1] and "pigmented purpuric lichenoid dermatitis of Gougerot and Blum"[1]) 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.[2]:829 Relative to other variants, it is characterized clinically by a male predominance, pruritus, with a predilection for the legs, and histologically, it features a densely cellular lichenoid infiltrate.[3]

It was characterized in 1925.[4]

Gougerot–Blum syndrome is named after the French dermatologists Henri Gougerot (1881–1955) and Paul Blum (1878–1933).

See also

References

  1. 1 2 Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
  2. ↑ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
  3. ↑ Barnhill RL and Crowson AN (eds) Textbook of Dermatopathology, second edition, McGraw-Hill, 2004: 211-212
  4. ↑ synd/2079 at Who Named It?
Classification


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.