Skip to content
Surf Wiki
Save to docs
general/abnormalities-of-dermal-fibrous-and-elastic-tissue

From Surf Wiki (app.surf) — the open knowledge base

Elastosis perforans serpiginosa


FieldValue
nameElastosis perforans serpiginosa
synonymsEPS
imageElastosis perforans serpiginosa.jpg
image_size150px
captionElastosis perforans serpiginosa: Hyperkeratotic plaque of papules

Elastosis perforans serpiginosa is a unique perforating disorder characterized by transepidermal elimination of elastic fibers and distinctive clinical lesions, which are serpiginous in distribution and can be associated with specific diseases.

File:Histopathology of elastosis perforans serpiginosa.jpg|Histopathology of elastosis perforans serpiginosa: Degenerated elastic fibers and transepidermal perforating canals (arrow points at one of them) File:Autosomal dominant - en.svg|This condition is inherited in an autosomal dominant manner.

References

References

  1. "OMIM Entry - 130100 - ELASTOSIS PERFORANS SERPIGINOSA; EPS".
  2. (2012). "Histopathology of Pseudoxanthoma Elasticum and Related Disorders: Histological Hallmarks and Diagnostic Clues". Scientifica.
  3. Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). Page 1041. McGraw-Hill. {{ISBN. 0-07-138076-0.
  4. Rapini, Ronald P.. (2007). "Dermatology: 2-Volume Set". Mosby.
Info: Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

Want to explore this topic further?

Ask Mako anything about Elastosis perforans serpiginosa — get instant answers, deeper analysis, and related topics.

Research with Mako

Free with your Surf account

Content sourced from Wikipedia, available under CC BY-SA 4.0.

This content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.

Report