Difference between revisions of "Epidermal necrosis"
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Features: | Features: | ||
*Similar [[erythema multiforme]]. | *Similar [[erythema multiforme]]. | ||
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*[[WC]]: | |||
**[http://commons.wikimedia.org/wiki/File:Confluent_epidermal_necrosis_-_intermed_mag.jpg Confluent epidermal necrosis - intermed. mag. (WC)]. | |||
**[http://commons.wikimedia.org/wiki/File:Confluent_epidermal_necrosis_-_very_high_mag.jpg Confluent epidermal necrosis - very high mag. (WC)]. | |||
==Toxic epidermal necrolysis== | ==Toxic epidermal necrolysis== | ||
Revision as of 06:12, 5 October 2011
Epidermal necrosis is an important finding in dermatopathology. Full-thickness necrosis, especially is very serious.
General
Full thickness DDx:
- Erythema multiform (EM).
- Toxic epidermal necrolysis (TEN).
- Stevens-Johnson syndrome (SJS).
- Trauma.
- Others. (???)
Partial thickness DDx:
- Staphylococcal scalded skin syndrome.
- Trauma. (???)
- Others. (???)
Notes:
- SJS and TEN are on a spectrum, EM (depending on who you ask) is considered separate.
- These are signed-out as "confluent epidermal necrosis - see comment".
- Comment: The histomorphologic findings are consistent with EM/SJS/TEN.
- The clinical DDx of EM/SJS/TEN includes acute generalized exanthematous pustulosis (AGEP).
- These are signed-out as "confluent epidermal necrosis - see comment".
Erythema multiforme
- Abbreviated EM.
General
Features:[1]
- Hypersensitivity disorder due to a drug or infection.
- Associated with the following: HSV, Mycoplasma, Histoplasma, others.
Clinical:
- Target-like lesion.
Microscopic
Features:[1]
- Lymphocytic interface dermatitis (lymphocytes at the dermal-epidermal junction).
- Necrotic/degenerative keratinocytes - key feature.
- +/-Epidermal blistering.
- +/-Epidermal sloughing.
Images:
- WC:
Stevens-Johnson syndrome
- Abbreviated SJS.
General
Rx causes of SJS:
- NSAIDs.
- Anticonvulsants.
- Sulfonamides.
- Penicillins.
Microscopic
Features:
- Similar erythema multiforme.
Images:
- WC:
Toxic epidermal necrolysis
- Abbreviated TEN.
General
- TEN more severe form SJS.
Definition:
- >30% sheet-like epidermal detachment, diffuse erythema, severe mucous membrane involvement.
- Most TEN (80%) Rx-related, only 50% of SJS Rx-related.
Microscopic
Features:
- Like erythema multiforme - but usu. less inflammation.[2]
Staphylococcal scalded skin syndrome
- Abbreviated SSSS.
General
- Due to keratinocyte cell-cell adhesion loss in the superficial epidermis - caused by S. aureus.[3]
Clinical:
- Blisters
Microscopic
Features:[3]
- Superficial dermis separates from underlying tissue - looks artefactual.
- Minimal/scant inflammation is typical.[4]
Image:
See also
- Dermatopathology - an introduction to the topic.
- Non-malignant skin disease.
- Inflammatory skin disease.
References
- ↑ 1.0 1.1 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1189. ISBN 978-1416031215.
- ↑ S. Sade. 8 September 2011.
- ↑ 3.0 3.1 Nishifuji, K.; Sugai, M.; Amagai, M. (Jan 2008). "Staphylococcal exfoliative toxins: "molecular scissors" of bacteria that attack the cutaneous defense barrier in mammals.". J Dermatol Sci 49 (1): 21-31. doi:10.1016/j.jdermsci.2007.05.007. PMID 17582744.
- ↑ URL: http://dermatlas.med.jhmi.edu/derm/display.cfm?ImageID=2105774586. Accessed on: 22 September 2011.