Anetoderma

From Wikipedia, the free encyclopedia
  (Redirected from Jadassohn–Pellizzari anetoderma)
Jump to navigation Jump to search
Anetoderma
Other names(Anetoderma maculosa,[1] Anetoderma maculosa cutis,[1] Atrophia maculosa cutis,[1] and Macular atrophy[2])
SpecialtyDermatology Edit this on Wikidata

Anetoderma is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue.[2] Anetoderma comes in three types:

  • Primary anetoderma
    • Jadassohn–Pellizzari anetoderma is a benign condition with focal loss of dermal elastic tissue.[3] Jadassohn-Pellizzari is one of two major classifications of primary anetoderma, the other being Schweninger–Buzzi anetoderma. The difference between the two is that Jadassohn–Pellizzari anetoderma is preceded by inflammatory lesions.[1]
    • Schweninger–Buzzi anetoderma is a cutaneous condition characterized by loss of dermal elastic tissue.[1]
  • Secondary anetoderma
  • Familial anetoderma

See also[edit]

References[edit]

  1. ^ a b c d e Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
  2. ^ a b Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). Page 1027. McGraw-Hill. ISBN 0-07-138076-0.
  3. ^ Laumann, Anne; Minocha, Julia Sanger; Ho, Stephen C (2009-06-22). "Anetoderma". eMedicine. Web MD. Retrieved 17 December 2009.

External links[edit]

Classification
External resources