Difference between revisions of "Panniculitis"
Jump to navigation
Jump to search
m (→General) |
|||
| Line 83: | Line 83: | ||
*Uncommon. | *Uncommon. | ||
*Etiology: unknown. | *Etiology: unknown. | ||
**''Brinster''<ref name=pmid18948765>{{Cite journal | last1 = Brinster | first1 = NK. | title = Dermatopathology for the surgical pathologist: a pattern-based approach to the diagnosis of inflammatory skin disorders (part II). | journal = Adv Anat Pathol | volume = 15 | issue = 6 | pages = 350-69 | month = Nov | year = 2008 | doi = 10.1097/PAP.0b013e31818b1ac6 | PMID = 18948765 }}</ref> suggests an association, in some cases, with ''[[Mycobacterium tuberculosis]]'' and ''hepatitis C''. | |||
Clinical:<ref name=Ref_PCPBoD8_609>{{Ref PCPBoD8|609}}</ref> | Clinical:<ref name=Ref_PCPBoD8_609>{{Ref PCPBoD8|609}}</ref> | ||
Revision as of 19:55, 19 September 2011
Panniculitis is inflammation of the adipose tissue. It is encountered in dermatopathology specimens.
Classification
- Lobular - involve fat lobules.
- Septal - involve interlobular septae.
A simple general DDx
Septal:
Lobular:
- Erythema induratum.
- Self-inflicted trauma (factitial panniculitis).
- Systemic lupus erythematosus.
- Other.
DDx by type
Septal:
- Erythema nodosum.
- Scleroderma panniculitis, also morphea profunda.[1]
Lobular:[1]
- Infectious panniculitis.
- Erythema induratum.
- Lupus panniculitis.
- Pancreatic panniculitis.
- Alpha1-antitrypsin deficiency.
- Subcutaneous fat necrosis of the newborn.
- Sclerema neonatorum.
Specific conditions
Erythema nodosum
Causes - mnemonic NODOSUM:[2]
- NO cause (idiopathic) ~ 55% of cases.
- Drugs (sulfonamides, amoxicillin, oral contraceptives) ~ 5% of cases.
- Other infections - group A streptococci (streptococcal pharyngitis), Yersinia, chlamydia, mycobacteria, others ~ 30% of cases.
- Sarcoidosis ~ 7% of cases.
- Ulcerative colitis & Crohn's disease ~ 2% of cases.
- Malignancy (leukemia, Hodgkin's lymphoma) ~ 1% of cases
Microscopic
- Expanded septa between fat lobules - key (low power) feature.
- Neutrophils.
- Lymphocytes.
- Histiocytes.
- Fibrin.
Notes:
- No vasculitis.
- +/-Granulomas.[6]
DDx:
Images:
Morphea profunda
- AKA scleroderma panniculitis.
General
Main article: Scleroderma
- Think about the name... sclerotic (sclero-) dermis (-derma).
Microscopic
Features:[1]
- Septal fibrosis/expansion - key feature.
- Classically ~2-3x an adiposcyte thick.
- +/-Deep dermal perivascular lymphocytes and plasma cells.
DDx:
Erythema induratum
General
Features:[4]
- Uncommon.
- Etiology: unknown.
- Brinster[1] suggests an association, in some cases, with Mycobacterium tuberculosis and hepatitis C.
Clinical:[5]
- Classic location: posterior shins.
- Ulcerates and scars.
Microscopic
Features:[4]
- Predominantly lobular process with:[3]
- Necrotizing granulomatous inflammation.
- Necrotizing vasculitis of small/medium sized vessels (early).
DDx:
- Infection.
Images:
See also
References
- ↑ 1.0 1.1 1.2 1.3 Brinster, NK. (Nov 2008). "Dermatopathology for the surgical pathologist: a pattern-based approach to the diagnosis of inflammatory skin disorders (part II).". Adv Anat Pathol 15 (6): 350-69. doi:10.1097/PAP.0b013e31818b1ac6. PMID 18948765.
- ↑ 2.0 2.1 Schwartz, RA.; Nervi, SJ. (Mar 2007). "Erythema nodosum: a sign of systemic disease.". Am Fam Physician 75 (5): 695-700. PMID 17375516.
- ↑ 3.0 3.1 URL: http://www.medscape.com/viewarticle/440356_8. Accessed on: 11 September 2011.
- ↑ 4.0 4.1 4.2 Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1199. ISBN 978-1416031215.
- ↑ 5.0 5.1 Mitchell, Richard; Kumar, Vinay; Fausto, Nelson; Abbas, Abul K.; Aster, Jon (2011). Pocket Companion to Robbins & Cotran Pathologic Basis of Disease (8th ed.). Elsevier Saunders. pp. 609. ISBN 978-1416054542.
- ↑ 6.0 6.1 URL: http://missinglink.ucsf.edu/lm/DermatologyGlossary/erythema_nodosum.html. Accessed on: 11 September 2011.