Difference between revisions of "Inflammatory skin disorders"

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'''Inflammatory skin disorders''' are a significant part of [[dermatopathology]].  They lead to trepidation among pathologists that don't see lots of skin.
'''Inflammatory skin disorders''', also '''inflammatory skin diseases''', are a significant part of [[dermatopathology]].  They lead to trepidation among pathologists that don't see lots of skin.  Non-inflammatory skin disease is covered in ''[[dermatologic neoplasms]]'' and ''[[non-malignant skin disease]]''.


=Classification=
*Bullous.
*Interface.
*Nodular & diffuse.
*Spongiotic.
*Vasculitis.
*Perivascular.
*Panniculitis.
*Psoriasiform.
'''Tabular comparison of inflammatory skin disease (adapted from ''Brinster''<ref name=pmid18418089>{{cite journal |author=Brinster NK |title=Dermatopathology for the surgical pathologist: a pattern based approach to the diagnosis of inflammatory skin disorders (part I) |journal=Adv Anat Pathol |volume=15 |issue=2 |pages=76–96 |year=2008 |month=March |pmid=18418089 |doi=10.1097/PAP.0b013e3181664e8d |url=}}</ref><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>):'''
{| class="wikitable"
| '''Pattern'''
| '''Key histologic feature'''
| '''Subclassifications'''
| '''Example'''
| '''Image'''
|-
| [[Bullous disease|Bullous]]
| large "empty spaces"
| -subcorneal<br>-suprabasillar<br>-subepidermal
| -[[pemphigus foliaceus]]<br>-[[pemphigus vulgaris]]<br>-[[dermatitis herpetiformis]]
| [[Image:Pemphigus_vulgaris_-_low_mag.jpg|thumb|150px|center|[[pemphigus vulgaris|PV]] (WC)]]
|-
| [[Interface_dermatitides|Interface]]
| inflammation at DE junction
| -vacuolar (minimal)<br>-lichenoid (band-like)
| -[[erythema multiforme]], [[SLE]]<br>-[[lichen planus]]
| [[Image:Vacuolar interface dermatitis - high mag.jpg|thumb|center|150px|[[vacuolar interface dermatitis|VID]] (WC)]]
|-
| [[Nodular and diffuse dermatitides|Nodular & diffuse]]
| intradermal inflammatory infiltrate - nodular and/or diffuse
| -neutrophic<br>-lymphocytic<br>-plasmic<br>-eosinophilic<br>-histocytic
| -follicular occlusion triad, ruptured cyst/follicle<br>-[[CTCL]], reactive<br>-[[plasma cell neoplasm]], [[syphilis]]<br>-eosinophilic cellulitis, [[Kimura disease]]<br>-[[granuloma annulare]], [[sarcoidosis]], [[TB]]
| [[Image:Cutaneous_T-cell_lymphoma_-_very_high_mag.jpg|thumb|center|110px|[[CTCL]] (WC)]]
|-
| [[Spongiotic_dermatitides|Spongiotic]]
| small empty spaces between keratinocytes - can see squamous bridges (best seen at high power); +/- quasi-microvacuolar appearance
| -acute<br>-subacute<br>-chronic
| -poison ivy<br>-nummular dermatitis<br>-[[atopic dermatitis]]
| [http://commons.wikimedia.org/wiki/File:Spongiotic_dermatitis_%282%29_Dyshidrotic_.JPG severe (WC)], [http://commons.wikimedia.org/wiki/File:Spongiotic_dermatitis_-_very_high_mag.jpg mild (WC)]
|-
| [[Vasculitis]]
| inflammation of vessel wall/vessel was destruction
| -small vessel <br> -medium vessel <br> -large vessel
| -[[leukocytoclastic vasculitis]]<br>-[[PAN]]<br>-[[giant cell arteritis]]
| [[Image:Churg-Strauss_syndrome_-_high_mag.jpg |thumb|150px|[[Eosinophilic granulomatosis with polyangiitis|EGPA]] (WC)]]
|-
| [[Dermatitides_with_perivascular_inflammation|Perivascular]]
| inflammation around vessels
| -neutrophilic<br>-lymphocytic<br>-mastocytic<br>-eosinophilic
| -[[cellulitis]]<br>-viral exanthem, Rx reaction<br>-[[mastocytosis]]<br>-insect bite, Rx reaction
| [[Image:Dermal_perivascular_lymphoeosinophilic_infiltrate_-_high_mag.jpg |thumb|center|110px|DPLI (WC)]]
|-
| [[Panniculitis]]
| inflammation of adipose tissue
| -septal<br>-lobular
| -[[erythema nodosum]], [[scleroderma panniculitis]]<br>-[[erythema induratum]], infection
|
|-
| [[Psoriasiform dermatitides|Psoriasiform]]
| epidermal thickening<br>and long rete ridges
| -regular<br>-irregular
| -[[psoriasis]]<br>-[[lichen simplex chronicus]]
| [[Image:Lichen_simplex_chronicus_-_very_low_mag.jpg|thumb|150px|center|[[Lichen simplex chronicus|LSC]] (WC)]]
|}
Notes:
*''DE junction'' = dermal-epidermal junction.
*The "empty space" in bullous disease ''in situ'' is filled with fluid.
=Non-specific patterns=
==Psoriasiform pattern==
===General===
*Can be subclassified.
DDx:
*Psoriasis vulgaris (most common).
*Psoriatic arthritis.
*Drug-induced.
*[[Dermatomycosis]] (fungal infection).
*Others.
===Microscopic===
Features:<ref>{{Ref PBoD8|1191}}</ref><ref name=pmid18418089>{{cite journal |author=Brinster NK |title=Dermatopathology for the surgical pathologist: a pattern based approach to the diagnosis of inflammatory skin disorders (part I) |journal=Adv Anat Pathol |volume=15 |issue=2 |pages=76–96 |year=2008 |month=March |pmid=18418089 |doi=10.1097/PAP.0b013e3181664e8d |url=}}</ref>
*Regular epidermal thickening - as very long rete ridges (described as "test tube-morphology") - '''key feature'''.
**Epidermis between rete ridges thin ("thinning of suprapapillary plate").
*Parakeratosis.
*Thin/absent granular layer.
*Dilated blood vessels in superficial dermis.
*Neutrophil clusters (Munro microabscess).
=Specific diseases=
==Seborrheic dermatitis==
===General===
*Very common.
===Microscopic===
Features:<ref>{{Ref PBoD8|1191}}</ref>
*[[Spongiosis]] (epidermal edema).
*Acanthosis (epidermal thickening).
*"Follicular lipping" = parakeratosis with neutrophils.
*Perivascular neutrophils and lymphocytes.
==Lupus erythematosus==
===General===
*A group of skin diseases - includes:
**The systemic disease, [[systemic lupus erythematosus]], that typically has multi-organ involvement.
===Microscopic===
Features - classic:
*Lymphocytic interface dermatitis.<ref>JAH. 20 February 2009.</ref>
*Basal layer vacuolization.<ref name=pmid18384217>{{cite journal |author=Crowson AN, Magro CM, Mihm MC |title=Interface dermatitis |journal=Arch. Pathol. Lab. Med. |volume=132 |issue=4 |pages=652–66 |year=2008 |month=April |pmid=18384217 |doi= |url=http://www.archivesofpathology.org/doi/full/10.1043/1543-2165%282008%29132%5B652%3AID%5D2.0.CO%3B2}}</ref>
*Intradermal mucin.
*Thin epidermis.
*Compact stratum corneum.
DDx:
*[[Discoid lupus erythematosus]].
*Drug reaction (drug-induced lupus erythematosus).
*[[Solar elastosis]] - may be confused with ''mucin''; vacuolar interface dermatitis ''not'' present
====Images====
<gallery>
Image:Vacuolar_interface_dermatitis_-_low_mag.jpg | Vacuolar interface dermatitis with dermal mucin - low mag. (WC)
Image:Vacuolar_interface_dermatitis_-_intermed_mag.jpg | Vacuolar interface dermatitis with dermal mucin - intermed. mag. (WC)
Image:Vacuolar_interface_dermatitis_-_high_mag.jpg | Vacuolar interface dermatitis with dermal mucin - high mag. (WC)
Image:Vacuolar_interface_dermatitis_-_very_high_mag.jpg | Vacuolar interface dermatitis with dermal mucin - very high mag. (WC)
</gallery>
==Discoid lupus erythematosus==
===General===
*Typically self-limited and isolated.
**It is '''not''' associated with ''[[systemic lupus erythematosus]]''.
===Microscopic===
Features:<ref>URL: [http://www.dermpedia.org/baby-dermpedia-for-beginners/discoid-lupus-erythematosus http://www.dermpedia.org/baby-dermpedia-for-beginners/discoid-lupus-erythematosus]. Accessed on: 7 March 2012.</ref>
*Lymphocytic interface dermatitis with basal layer vacuolation and keratinocyte apoptosis.
*Deep dermal lymphocytes.
*Basket weave stratum corneum.
*Dermal mucin.
*Thick dermal-epidermal basement membrane.
DDx:
*[[Lupus erythematosus]].
Image:
*[http://www.dermpedia.org/baby-dermpedia-for-beginners/discoid-lupus-erythematosus DLE (dermpedia.org)].
==Dermatomyositis==
:''For the muscle manifestations see: [[Neuromuscular_pathology#Dermatomyositis]]''.
===General===
*Complement mediated disease - membrane attack complex.
*Usually middle age.
*Associated skin rash is common.
**May precede or follow muscle pathology.
*Associated with malignancy in approximately 10% of cases.<ref name=pmid20398365>{{cite journal |author=Chen YJ, Wu CY, Huang YL, Wang CB, Shen JL, Chang YT |title=Cancer risks of dermatomyositis and polymyositis: a nationwide cohort study in Taiwan |journal=Arthritis Res. Ther. |volume=12 |issue=2 |pages=R70 |year=2010 |pmid=20398365 |pmc=2888225 |doi=10.1186/ar2987 |url=}}</ref>
Clinical:
*Jo-1 +ve.
===Gross===
*Have lesions on the knuckles - ''Gottron's papules''.
===Microsopic===
Features:
*Vacuolar interface dermatitis (lymphocytic inflammation at the dermal-epidermal junction).
*+/-Loss of rete ridges.
DDx:
*Lupus.
==Lichen planus==
:''Should '''not''' be confused with [[lichen planus-like keratosis]]''.
*Abbreviated ''LP''.
===General===
*An [[oral pathology]] - classically.
*May be seen where the sun don't shine - [[penis]],<ref name=pmid20082512>{{Cite journal  | last1 = Teichman | first1 = JM. | last2 = Sea | first2 = J. | last3 = Thompson | first3 = IM. | last4 = Elston | first4 = DM. | title = Noninfectious penile lesions. | journal = Am Fam Physician | volume = 81 | issue = 2 | pages = 167-74 | month = Jan | year = 2010 | doi =  | PMID = 20082512 }}</ref> [[vulva]] and [[vagina]].<ref name=pmid20062629>{{Cite journal  | last1 = Gupta | first1 = R. | last2 = Bansal | first2 = B. | last3 = Singh | first3 = S. | last4 = Yadav | first4 = I. | last5 = Gupta | first5 = K. | last6 = Kudesia | first6 = M. | title = Lichen planus of uterine cervix - the first report of a novel site of occurrence: a case report. | journal = Cases J | volume = 2 | issue =  | pages = 9306 | month =  | year = 2009 | doi = 10.1186/1757-1626-2-9306 | PMID = 20062629 }}</ref>
Etiology:
*Autoimmune disease, T-cell–mediated.<ref>URL: [http://emedicine.medscape.com/article/1078327-overview http://emedicine.medscape.com/article/1078327-overview]. Accessed on: 11 September 2010.</ref>
Clinical:<ref name=Ref_PBoD8_1191>{{Ref PBoD8|1191}}</ref>
*6 Ps: pruritic (itchy), purple, polygonal, planar papules and plaques.
Note:
*Clinically, lichen planus and [[lichen sclerosus]] are similar. The main difference is lichen planus involves mucous membranes.<ref name=pmid20868406>{{Cite journal  | last1 = McPherson | first1 = T. | last2 = Cooper | first2 = S. | title = Vulval lichen sclerosus and lichen planus. | journal = Dermatol Ther | volume = 23 | issue = 5 | pages = 523-32 | month =  | year =  | doi = 10.1111/j.1529-8019.2010.01355.x | PMID = 20868406 }}</ref>
===Gross===
*Wickham striae = white lines/dots.
**Due to hypergranulosis.
===Microscopic===
Features:<ref>URL: [http://emedicine.medscape.com/article/1078327-overview http://emedicine.medscape.com/article/1078327-overview]. Accessed on: 11 September 2010.</ref><ref name=Ref_PBoD8_1192>{{Ref PBoD8|1192}}</ref>
*Loss of basal cells (stratum basale) -- '''key feature'''.
*Loss of rete ridges/formation of pointed rete ridges "sawtoothing".
*Interface dermatitis (lymphocytes at dermal-epidermal junction).
*Hypergranulosis; stratum granulosum thickened (grossly seen as "Wickham stria" = white lines).
*Hyperkeratosis; stratum corneum thickened.
*Necrotic basal cell in dermis = colloid bodies = Civatte bodies.<ref name=Ref_PCPBoD8_604>{{Ref PCPBoD8|604}}</ref>
**Pink bodies approximately the size of a keratinocyte.
Notes:
*Hyperkeratosis and hypergranulosis are not seen in [[erythema multiforme]].
*Colloid bodies = cytoid bodies = Civatte bodies = hyaline bodies = apoptotic bodies.<ref>URL: [http://www.careforumwales.org/cell-carcinoma/histopathologic-terminology.html http://www.careforumwales.org/cell-carcinoma/histopathologic-terminology.html]. Accessed on: 28 August 2011.</ref>
**DDx: [[systemic lupus erythematosus]], [[lichen planus]], and [[graft-versus-host disease]].
DDx:
*[[Bullous disease]], subepithelial vesicular.
*[[Lichenoid keratosis]] (lichen planus-like keratosis) - parakeratosis prominent, no oral mucosal involvement.
*Fungal infection.<ref name=Ref_Derm36>{{Ref Derm|36}}</ref>
*Lichenoid drug reaction - unusual body site affected, separated clinically.
*Lichenoid [[actinic keratosis]] - basal atypia, [[solar elastosis]].
====Images====
<gallery>
Image:Lichen_planus_intermed_mag.jpg | Lichen planus - intermed. mag. (WC/Nephron)
Image:Lichen_planus_low_mag.jpg | Lichen planus - low mag. (WC/Nephron)
</gallery>
===Stains===
*PAS-D or PAS-F to exclude a fungal infection.
===Sign out===
<pre>
FORESKIN, CIRCUMCISION:
- LICHEN PLANUS.
</pre>
<pre>
VULVA, LEFT POSTERIOR FOURCHETTE, BIOPSY:
- COMPATIBLE WITH LICHEN PLANUS.
</pre>
====Micro====
The sections show skin with a lymphoplasmacytic interface dermatitis, basal cell loss, hypergranulosis, hyperkeratosis, loss of the rete ridges and Civatte bodies.
The epidermis matures to the surface. No significant nuclear atypia is identified.
Fungal organisms are not identified with a PAS-D stain.
==Lichen sclerosus==
{{Main|Lichen sclerosus}}
===Microscopic===
Features:<ref name=Ref_PBoD1065-6>{{Ref PBoD|1065-6}}</ref>
*Subepithelial fibrosis - '''key feature'''.
==Psoriasis==
===General===
*Chronic skin condition +/- systemic involvement:<ref name=Ref_PCPBoD8_603>{{Ref PCPBoD8|603}}</ref>
**[[Arthritis]], i.e. psoriatic arthritis.
**[[Myopathy]].
**Enteropathy, e.g. [[inflammatory bowel disease]].
**Syondylitic joint disease (spondylos = vertebrae<ref>URL: [http://medical-dictionary.thefreedictionary.com/spondylosis http://medical-dictionary.thefreedictionary.com/spondylosis]. Accessed on: 28 August 2011.</ref>).
*Other considerations:
**Drug-induced psoriasis.<ref name=pmid21489366>{{Cite journal  | last1 = Milavec-Puretić | first1 = V. | last2 = Mance | first2 = M. | last3 = Ceović | first3 = R. | last4 = Lipozenčić | first4 = J. | title = Drug induced psoriasis. | journal = Acta Dermatovenerol Croat | volume = 19 | issue = 1 | pages = 39-42 | month = Mar | year = 2011 | doi =  | PMID = 21489366 }}</ref>
====Clinical====
*''Auspitz sign'' = pin-point bleeding on removal of scale.
*''Koebner phenomenon'' = lesions form at site of trauma.
Common locations:<ref name=Ref_PCPBoD8_603>{{Ref PCPBoD8|603}}</ref>
*Knees, elbows, scalp, glans [[penis]].
===Microscopic===
Features:<ref name=Ref_PCPBoD8_603>{{Ref PCPBoD8|603}}</ref>
*"Regular" acanthosis + long rete ridges (psoriasiform hyperplasia).
**"Regular" ([[Psoriasiform dermatitides|psoriasiform change]]) = rete ridges are of similar length and thickness.
*Parakeratosis.
*Dilated vessels in superficial dermis (give rise to ''Auspitz sign'').
*Spongiform pustules = [[PMN]]s in stratum spinosum.
*PMNs in parakeratotic stratum corneum (Munro microabscess).
*Thinning of the suprapapillary plate.
**The epidermis between rete ridges is thinner than in the normal adjacent skin - '''key feature'''.
DDx:
*[[Dermatomycosis]] ([[Fungi|fungal infection]]).
*Drug reaction.
Note:
*[[Dermatophytosis]] = ring worm; dermatophystosis != [[dermatomycosis]].
====Images====
www:
*[http://missinglink.ucsf.edu/lm/dermatologyglossary/img/Dermatology%20Glossary/Glossary%20Histo%20Images/Psoriasis_low_power.jpg Psoriasis - low mag. (ucsf.edu)].<ref>URL: [http://missinglink.ucsf.edu/lm/dermatologyglossary/psoriasis.html http://missinglink.ucsf.edu/lm/dermatologyglossary/psoriasis.html]. Accessed on: 4 September 2013.</ref>
===Stains===
*[[PASD stain]] -ve for [[fungi|fungal]] organisms.
===Sign out===
<pre>
SKIN LESION, LEFT ARM, PUNCH BIOPSY:
- SKIN WITH ACANTHOSIS, HYPERKERATOSIS, FOCAL PARAKERATOSIS, PROMINENT
  DILATED VESSELS IN THE SUPERFICIAL DERMIS, SUPERFICIAL SPONGIFORM PUSTULES.
- MILD NONSPECIFIC PERIVASCULAR INFLAMMATION.
- NEGATIVE FOR FUNGAL ORGANISMS WITH PAS STAINING.
COMMENT:
The findings are compatible with psoriasis. 
</pre>
====Micro====
The sections show skin with regular psoriasiform change, hyperkeratosis, focal parakeratosis, prominent dilated vessels in the superficial dermis, superficial clusters of intraepidermal neutrophils (spongiform pustules) and thinning of the suprapapillary plate is present. A few perivascular inflammatory cells are present.
There is no epidermal necrosis. Eosinophils are not apparent. The lymphocytes do not have significant atypia.
==Lichen striatus==
===General===
Features:<ref name=pmid15283785>{{Cite journal  | last1 = Taniguchi Abagge | first1 = K. | last2 = Parolin Marinoni | first2 = L. | last3 = Giraldi | first3 = S. | last4 = Carvalho | first4 = VO. | last5 = de Oliveira Santini | first5 = C. | last6 = Favre | first6 = H. | title = Lichen striatus: description of 89 cases in children. | journal = Pediatr Dermatol | volume = 21 | issue = 4 | pages = 440-3 | month =  | year =  | doi = 10.1111/j.0736-8046.2004.21403.x | PMID = 15283785 }}</ref>
*Benign, self-limited.
Clinical:
*Linear rash usu. on lower extremity.
*Associated with atopy, [[lichen sclerosus]].<ref name=pmid15283785/>
*Children.
Clinical image:
*[http://perridermatology.com/blog/2011/3/7/lichen-planus-lichen-striatus.html LS (perridermatology.com)].
===Microscopic===
Features:
*"Ball and glove" pattern:
**Rete ridges (glove) surround nexts of lymphocytes (ball).
*Hyperkeratosis.
*Parakeratosis.
DDx:
*[[Lichen planus]].
Images:
*[http://www.dermpathdiagnostics.com/dxref.asp?catid=25&id=57 Lichen striatus (dermpathdiagnostics.com)].
*[http://www.drmihm.com/cases/case.cfm?CaseID=42 Lichen striatus (drmihm.com)].
==Lichen aureus==
===General===
*Rare.
Clinical:<ref name=pmid17511956/>
*Plaques + minimal scale - erythematous/golden.
===Microscopic===
Features:<ref name=pmid17511956>{{Cite journal  | last1 = Hazan | first1 = C. | last2 = Fangman | first2 = B. | last3 = Cohen | first3 = D. | title = Lichen aureus. | journal = Dermatol Online J | volume = 13 | issue = 1 | pages = 23 | month =  | year = 2007 | doi =  | PMID = 17511956 | URL = http://dermatology.cdlib.org/131/cases/NYUcases/051606_9.html }}</ref>
*Lymphocyte-predominant perivascular pattern.
**May have features suggestive of vacuolar interface pattern.
*Fibrosis of superficial papillary dermis.
Images:
*[http://dermatology.cdlib.org/131/cases/NYUcases/051606_9.html Lichen aureus (cdlib.org)].
==Granuloma faciale==
===General===
*Considered a [[vasculitis]].<ref name=dermatlas_gf>URL: [http://dermatlas.med.jhmi.edu/derm/indexDisplay.cfm?ImageID=1289066309 http://dermatlas.med.jhmi.edu/derm/indexDisplay.cfm?ImageID=1289066309]. Accessed on: 23 September 2011.</ref>
===Microscopic===
Features:<ref name=Ref_Derm198-9>{{Ref Derm|198-9}}</ref>
*Neutrophilic vasculitis - often subtle:
**Neutrophils within blood vessel walls.
**Vessels destruction ([[fibrinoid necrosis]] or nuclear dust).
*Mixed inflammatory superficial dermal infiltrate.
**Eosinophils, neutrophils, plasma cells, histiocytes.
*Lesion separated from the (normal) epidermis (Grenz zone).<ref name=dermatlas_gf>URL: [http://dermatlas.med.jhmi.edu/derm/indexDisplay.cfm?ImageID=1289066309 http://dermatlas.med.jhmi.edu/derm/indexDisplay.cfm?ImageID=1289066309]. Accessed on: 23 September 2011.</ref>
DDx of chronic fibrosing [[leukocytoclastic vasculitis]]:<ref name=Ref_Derm198-9>{{Ref Derm|198-9}}</ref>
*Granuloma faciale.
*Erythema elevatum diutinum - lacks Grenz zone.
*Inflammatory pseudotumour.
Image:
*[http://dermatlas.med.jhmi.edu/derm/indexDisplay.cfm?ImageID=1289066309 Granuloma faciale (dermatlas.med.jhmi.edu)].
==Atopic dermatitis==
*[[AKA]] ''atopic eczema'', [[AKA]] ''infantile eczema''.
===General===
*Very common - especially in children.<ref name=ad_nih>URL: [http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001856/ http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001856/]. Accessed on: 28 December 2011.</ref>
**Most children outgrow the condition.
===Microscopic===
Features:
*Spongiotic dermatitis.
DDx:
*[[Spongiotic dermatitides]].
====Images====
<gallery>
Image:Spongiotic_dermatitis_-_high_mag.jpg | Mild spongiotic dermatitis - high mag. (WC)
Image:Spongiotic_dermatitis_-_very_high_mag.jpg | Mild spongiotic dermatitis - very high mag. (WC)
</gallery>
==Sweet syndrome==
===General===
*Uncommon.
===Microscopic===
Features:
*Nodular and diffuse pattern - neutrophils predominant - without pus.
DDx ''rips'':
*Rheumatoid neutrophilic dermatitis.
*[[Bowel-associated dermatosis-arthritis syndrome]] (BADAS).
*[[Pyoderma gangrenosum]].
*Sweet syndrome.
Image:
*[http://dermatology.cdlib.org/94/NYU/Apr2002/041602-7b.jpg Sweet syndrome (cdlib.org)].<ref>URL: [http://dermatology.cdlib.org/94/NYU/Apr2002/7.html http://dermatology.cdlib.org/94/NYU/Apr2002/7.html]. Accessed on: 4 January 2012.</ref>
==Granuloma inguinale==
:'''Not''' to be confused with ''[[granuloma annulare]]''.
*Previously known as ''donovanosis''.
===General===
*Infection caused by ''Klebsiella granulomatis'' - [[Gram stain|Gram]]-negative, rod-shaped bacteria.
**Used to be known as ''Calymmatobacterium granulomatis''.<ref name=pmid12473810>{{cite journal |author=O'Farrell N |title=Donovanosis |journal=Sex Transm Infect |volume=78 |issue=6 |pages=452–7 |year=2002 |month=December |pmid=12473810 |pmc=1758360 |doi= |url=http://sti.bmj.com/cgi/pmidlookup?view=long&pmid=12473810}}</ref>
Location:
*[[Penis]].
*[[Vulva]].
Clinical:<ref name=pmid21738983>{{Cite journal  | last1 = Bezerra | first1 = SM. | last2 = Jardim | first2 = MM. | last3 = Silva | first3 = VB. | title = Granuloma inguinale (Donovanosis). | journal = An Bras Dermatol | volume = 86 | issue = 3 | pages = 585-6 | month = Jun | year = 2011 | doi =  | PMID = 21738983 |URL = http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962011000300028&lng=en&nrm=iso&tlng=en }}</ref>
*Sexually transmitted.
*Nodule or papule developing into a painless ulcer in the inguinal region.
*No lymphadenopathy (unlike [[syphilis]]).
===Microscopic===
Features:
*Donovan bodies - '''key feature''':
**Rod-shaped bodies within histiocytes.
DDx:
*[[Syphilis]].
Image:
*[http://microblog.me.uk/213 Granuloma inguinale - crappy image (microblog.me.uk)].
===Stains===
*[[Giemsa stain]] - highlights organisms.
==Pyoderma gangrenosum==
{{Main|Pyoderma gangrenosum}}
==Necrobiotic xanthogranuloma==
*Abbreviated ''NXG''.
{{Main|Necrobiotic xanthogranuloma}}
=DDx for pattern=
==Spongiotic dermatitides==
==Spongiotic dermatitides==
DDx:<ref name=pmid18418089>{{cite journal |author=Brinster NK |title=Dermatopathology for the surgical pathologist: a pattern based approach to the diagnosis of inflammatory skin disorders (part I) |journal=Adv Anat Pathol |volume=15 |issue=2 |pages=76–96 |year=2008 |month=March |pmid=18418089 |doi=10.1097/PAP.0b013e3181664e8d |url=}}</ref>
DDx:<ref name=pmid18418089>{{cite journal |author=Brinster NK |title=Dermatopathology for the surgical pathologist: a pattern based approach to the diagnosis of inflammatory skin disorders (part I) |journal=Adv Anat Pathol |volume=15 |issue=2 |pages=76–96 |year=2008 |month=March |pmid=18418089 |doi=10.1097/PAP.0b013e3181664e8d |url=}}</ref>
*Atopic dermatitis.
*[[Atopic dermatitis]].
*Contact dermatitis.
*[[Contact dermatitis]].
*Stasis dermatitis.
*Stasis dermatitis.
*Seborrheic dermatitis.
*[[Seborrheic dermatitis]].
*Nummular dermatitis.
*Nummular dermatitis.
*Spongiotic drug eruption.
*Spongiotic drug eruption.
Line 15: Line 459:
*Psoriasis vulgaris.
*Psoriasis vulgaris.
*Dermatophyte infection.
*Dermatophyte infection.
*Pityriasis rubra pilaris.
*[[Pityriasis rubra pilaris]].


===Irregular psoriasiform dermatitis===
===Irregular psoriasiform dermatitis===
Line 32: Line 476:
*[[Systemic lupus erythematosus]].
*[[Systemic lupus erythematosus]].
*Morbillifrom viral exanthem.
*Morbillifrom viral exanthem.
Additional:<ref name=pmid16311340>{{Cite journal  | last1 = Alsaad | first1 = KO. | last2 = Ghazarian | first2 = D. | title = My approach to superficial inflammatory dermatoses. | journal = J Clin Pathol | volume = 58 | issue = 12 | pages = 1233-41 | month = Dec | year = 2005 | doi = 10.1136/jcp.2005.027151 | PMID = 16311340 | PMC = 1770784}}</ref>
*Phototoxic dermatitis.
*Acute radiation dermatitis.
*Erythema multiforme-like drug eruption.
*Lichen sclerosis et atrophicus.
*[[Erythema dyschromicum perstans]] (ashy dermatosis).
Super lame mnemonic ''Danny G & SLE'':
*'''D'''ermatomyositis, '''G'''VHD, '''S'''LE, '''L'''ichen sclerosus, '''E'''rythema multiforme.


===Lichenoid interface dermatitides===
===Lichenoid interface dermatitides===
Line 40: Line 494:
*Lichenoid drug eruption.
*Lichenoid drug eruption.
*Fixed drug eruption.
*Fixed drug eruption.
Additional:<ref name=pmid16311340>{{Cite journal  | last1 = Alsaad | first1 = KO. | last2 = Ghazarian | first2 = D. | title = My approach to superficial inflammatory dermatoses. | journal = J Clin Pathol | volume = 58 | issue = 12 | pages = 1233-41 | month = Dec | year = 2005 | doi = 10.1136/jcp.2005.027151 | PMID = 16311340 | PMC = 1770784}}</ref>
*[[Lichen planus-like keratosis]].
*Lichenoid [[actinic keratosis]].
*Lichen nitidus.
*Pigmented purpuric dermatosis.
*Lichen [[amyloidosis]].
*Pityriasis lichenoides chronica.
*[[HIV]] dermatitis.
*[[Syphilis]].
*[[Urticaria pigmentosa]].
*Chronic [[graft versus host disease]].


==Bullous disease==
==Bullous disease==
{{Main|Bullous disease}}
===Subcorneal bullous disorders===
===Subcorneal bullous disorders===
DDx '''with''' acantholysis:<ref name=pmid18418089/>
DDx '''with''' acantholysis:<ref name=pmid18418089/>
*[[Pemphigus foliaceous]].
*[[Pemphigus foliaceus]].
*[[Bullous impetigo.
*[[Bullous impetigo]].
*[[Staphylococcual scaled skin syndrome]].
*[[Staphylococcal scalded skin syndrome]].


DDx '''without''' acantholysis:DDx:<ref name=pmid18418089/>
DDx '''without''' acantholysis:DDx:<ref name=pmid18418089/>
*Subcorneal pustular demratosis (Sneddon-Wilkinson disease)
*Subcorneal pustular dermatosis (Sneddon-Wilkinson disease).
*Pustular psoriasis.
*Pustular psoriasis.
*Pustular drug eruption (acute generalized exanthematous pustulosis).
*Pustular drug eruption ([[acute generalized exanthematous pustulosis]]).


===Suprabasilar bullous disorders===
===Suprabasilar bullous disorders===
Line 59: Line 526:
*[[Darier disease]].
*[[Darier disease]].
*[[Grover disease]] (transient acantholytic dermatosis).
*[[Grover disease]] (transient acantholytic dermatosis).
Memory device - ''PhD'' + ''Grover'' = '''P'''emphigus vulgaris, '''H'''ailey-Hailey, '''D'''arier, '''G'''rover.


===Subepidermal bullous disorders===
===Subepidermal bullous disorders===
Line 66: Line 535:
*[[Porphyria cutanea tarda]].
*[[Porphyria cutanea tarda]].
*Epidermolysis bullosa acquista.
*Epidermolysis bullosa acquista.
*[[Dermatitis herpetiformsis]].
*[[Dermatitis herpetiformis]].
*Linear IgA disease.
*Linear IgA disease.


Line 74: Line 543:
*Bullous [[systemic lupus erythematosus]].
*Bullous [[systemic lupus erythematosus]].


==Perivascular inflammation==
Mnemonic ''DELPHI'':
*'''D'''ermatitis herpetiformis.
*'''E'''pidermolysis bullosa acquisita.
*Bullous '''l'''upus erythematosis.
*'''P'''emphigoid, bullous.
*'''H'''erpes gestationis - rare autoimmune bullous dermatosis of pregnancy, not related to HSV.<ref>URL: [http://emedicine.medscape.com/article/1063499-overview http://emedicine.medscape.com/article/1063499-overview]. Accessed on: 23 September 2011.</ref>
*Linear '''I'''gA disease.
 
==Dermatitides with perivascular inflammation==
===Lymphocytes===
===Lymphocytes===
Lymphocytes (tightly cuffed):<ref name=pmid18418089/>
Lymphocytes (tightly cuffed):<ref name=pmid18418089/>
Line 81: Line 558:
*Malignancy.
*Malignancy.
*Vitiligo (with absent melanocytes).
*Vitiligo (with absent melanocytes).
*Scleroderma/morphea.
*[[Scleroderma]]/morphea.


Lymphocytes & plasma cells +/-eosinophils:
Lymphocytes & plasma cells +/-eosinophils:
Line 94: Line 571:
*Insect bite.
*Insect bite.
*Dermatophyte infection.
*Dermatophyte infection.
A simple memory device - 6 Ls:<ref name=dermpathmd>URL: [http://www.dermpathmd.com/mnemonics/mnemonics_dermatopathology.htm http://www.dermpathmd.com/mnemonics/mnemonics_dermatopathology.htm]. Accessed on: 23 September 2011.</ref>
*'''L'''ymphoma.
*Pseudo'''l'''ymphoma (cutaneous lymphoid hyperplasia, lymphocytoma cutis).
*'''L'''upus erythematosus.
*'''L'''ymphocytic infiltrate of Jessner / tumid lupus erythematosus.
*[[polymorphous light eruption|Polymorphous '''l'''ight eruption]].
*'''L'''yme disease.


===Neutrophils===
===Neutrophils===
DDx:<ref name=pmid18418089/>
DDx:<ref name=pmid18418089/>
*Cellulitis.
*[[Cellulitis]].
*Neutrophilic eccrine hidradenitis (idiopathic palmar-plantar hidradenitis)
*Neutrophilic eccrine hidradenitis (idiopathic palmar-plantar hidradenitis)


Line 105: Line 590:
===Eosinophils===
===Eosinophils===
DDx:<ref name=pmid18418089/>
DDx:<ref name=pmid18418089/>
*Hypersensitivity reaction/drug reaction.
*[[Hypersensitivity]] reaction/drug reaction.
*Insect bite.
*Insect bite.
*Bullous pemphigoid, urticarial.
*Bullous pemphigoid, urticarial.
Line 115: Line 600:
{{Main|Vasculitides}}
{{Main|Vasculitides}}


General DDx:
*Infection.
*Autoimmune.
*Malignancy.
*Toxic (medications).
Small vessel:
*[[Small vessel leukocytoclastic vasculitis]] (LCV).
Medium vessel:
*[[Polyarteritis nodosa]].
*[[Wegener's granulomatosis]].
Medium vessels often with small vessel involvement:
*[[Churg-Strauss syndrome]].
*[[Microscopic polyangiitis]].
*Mixed cryoglobulinemia.
*[[Connective tissue diseases]].
Large vessel:
*[[Giant cell arteritis]].
==Nodular and diffuse dermatitides==
===Neutrophils===
====With pus (suppurative)====
Neutrophils only:
*Follicular occlusion triad.
*Ruptured cyst/follicle.
Neutrophils and eosinophils:
*Halogenoderma.
*Blastomycosis-like pyoderma (pyoderma vegetans) - due to bacterial infection, usu. ''S. aureus''.
====Without pus====
With vasculitis:
*Neutrophils only: see ''[[vasculitides]]''.
*Mixed infiltrate: [[granuloma faciale]], erythema elevatinum diutinum.
Without vasculitis:
*[[Sweet syndrome]].
*[[Pyoderma gangrenosum]].
*[[Rheumatoid arthritis|Rheumatoid neutrophilic dermatitis]].
*Bowel-associated dermatosis-arthritis syndrome.
===Lymphocytes===
*Reactive lymphoid hyperplasia - may be due to drugs.
*[[Lymphoma|Lymphoid malignancy]].
===Plasma cells===
*Inflammation.
*[[Plasma cell neoplasm]]s.
*Infections:
**[[Syphilis]] - lichenoid/psoriasiform pattern.
**[[Chancroid]].
**[[Granuloma inguinale]].
**[[Lymphogranuloma venereum]].
===Eosinophils===
*Eosinophilic cellulitis (Wells syndrome).
**Insect bites.
*Hypereosinophilic syndrome (HES).
*[[Angiolymphoid hyperplasia with eosinophilia]] (ALHE).
*[[Kimura disease]].
===Histiocytes===
====Granulomatous====
=====Sarcoidal=====
*[[Sarcoidosis]] - have few lymphoid cells around them; thus called "naked granulomas".<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>
=====Tuberculoid=====
*[[Tuberculosis]].
*Tertiary [[syphilis]] - usu. abundant plasma cells.
*Cutaneous leishmaniasis.
=====Foreign body-type granulomas=====
=====Palisaded granumolas=====
Blue granuloma:
*[[Granuloma annulare]].
*[[Wegener granulomatosis]].
*Rheumatoid vasculitis.
Red granuloma:
*[[Rheumatoid nodule]].
*[[Necrobiosis lipoidica]].
*[[Necrobiotic xanthogranuloma]].
*[[Churg-Strauss syndrome]].


=See also=
=See also=
Line 122: Line 692:
=References=
=References=
{{Reflist|2}}
{{Reflist|2}}
=External links=
*[http://www.dermpathmd.com/mnemonics/mnemonics_dermatopathology.htm Dermatopathology mnemonics (dermpathmd.com)].


[[Category:Dermatopathology]]
[[Category:Dermatopathology]]

Latest revision as of 22:18, 5 December 2018

Inflammatory skin disorders, also inflammatory skin diseases, are a significant part of dermatopathology. They lead to trepidation among pathologists that don't see lots of skin. Non-inflammatory skin disease is covered in dermatologic neoplasms and non-malignant skin disease.

Classification

  • Bullous.
  • Interface.
  • Nodular & diffuse.
  • Spongiotic.
  • Vasculitis.
  • Perivascular.
  • Panniculitis.
  • Psoriasiform.

Tabular comparison of inflammatory skin disease (adapted from Brinster[1][2]):

Pattern Key histologic feature Subclassifications Example Image
Bullous large "empty spaces" -subcorneal
-suprabasillar
-subepidermal 		-pemphigus foliaceus
-pemphigus vulgaris
-dermatitis herpetiformis
PV (WC)
Interface inflammation at DE junction -vacuolar (minimal)
-lichenoid (band-like) 		-erythema multiforme, SLE
-lichen planus
VID (WC)
Nodular & diffuse intradermal inflammatory infiltrate - nodular and/or diffuse -neutrophic
-lymphocytic
-plasmic
-eosinophilic
-histocytic 		-follicular occlusion triad, ruptured cyst/follicle
-CTCL, reactive
-plasma cell neoplasm, syphilis
-eosinophilic cellulitis, Kimura disease
-granuloma annulare, sarcoidosis, TB
CTCL (WC)
Spongiotic small empty spaces between keratinocytes - can see squamous bridges (best seen at high power); +/- quasi-microvacuolar appearance -acute
-subacute
-chronic 		-poison ivy
-nummular dermatitis
-atopic dermatitis 		severe (WC), mild (WC)
Vasculitis inflammation of vessel wall/vessel was destruction -small vessel
-medium vessel
-large vessel 		-leukocytoclastic vasculitis
-PAN
-giant cell arteritis
EGPA (WC)
Perivascular inflammation around vessels -neutrophilic
-lymphocytic
-mastocytic
-eosinophilic 		-cellulitis
-viral exanthem, Rx reaction
-mastocytosis
-insect bite, Rx reaction
DPLI (WC)
Panniculitis inflammation of adipose tissue -septal
-lobular 		-erythema nodosum, scleroderma panniculitis
-erythema induratum, infection
Psoriasiform epidermal thickening
and long rete ridges 		-regular
-irregular 		-psoriasis
-lichen simplex chronicus
LSC (WC)

Notes:

  • DE junction = dermal-epidermal junction.
  • The "empty space" in bullous disease in situ is filled with fluid.

Non-specific patterns

Psoriasiform pattern

General

  • Can be subclassified.

DDx:

  • Psoriasis vulgaris (most common).
  • Psoriatic arthritis.
  • Drug-induced.
  • Dermatomycosis (fungal infection).
  • Others.

Microscopic

Features:[3][1]

  • Regular epidermal thickening - as very long rete ridges (described as "test tube-morphology") - key feature.
    • Epidermis between rete ridges thin ("thinning of suprapapillary plate").
  • Parakeratosis.
  • Thin/absent granular layer.
  • Dilated blood vessels in superficial dermis.
  • Neutrophil clusters (Munro microabscess).

Specific diseases

Seborrheic dermatitis

General

  • Very common.

Microscopic

Features:[4]

  • Spongiosis (epidermal edema).
  • Acanthosis (epidermal thickening).
  • "Follicular lipping" = parakeratosis with neutrophils.
  • Perivascular neutrophils and lymphocytes.

Lupus erythematosus

General

Microscopic

Features - classic:

  • Lymphocytic interface dermatitis.[5]
  • Basal layer vacuolization.[6]
  • Intradermal mucin.
  • Thin epidermis.
  • Compact stratum corneum.

DDx:

Images

  • Vacuolar interface dermatitis with dermal mucin - low mag. (WC)

  • Vacuolar interface dermatitis with dermal mucin - intermed. mag. (WC)

  • Vacuolar interface dermatitis with dermal mucin - high mag. (WC)

  • Vacuolar interface dermatitis with dermal mucin - very high mag. (WC)

Discoid lupus erythematosus

General

Microscopic

Features:[7]

  • Lymphocytic interface dermatitis with basal layer vacuolation and keratinocyte apoptosis.
  • Deep dermal lymphocytes.
  • Basket weave stratum corneum.
  • Dermal mucin.
  • Thick dermal-epidermal basement membrane.

DDx:

Image:

Dermatomyositis

For the muscle manifestations see: Neuromuscular_pathology#Dermatomyositis.

General

  • Complement mediated disease - membrane attack complex.
  • Usually middle age.
  • Associated skin rash is common.
    • May precede or follow muscle pathology.
  • Associated with malignancy in approximately 10% of cases.[8]

Clinical:

  • Jo-1 +ve.

Gross

  • Have lesions on the knuckles - Gottron's papules.

Microsopic

Features:

  • Vacuolar interface dermatitis (lymphocytic inflammation at the dermal-epidermal junction).
  • +/-Loss of rete ridges.

DDx:

  • Lupus.

Lichen planus

Should not be confused with lichen planus-like keratosis.
  • Abbreviated LP.

General

Etiology:

  • Autoimmune disease, T-cell–mediated.[11]

Clinical:[12]

  • 6 Ps: pruritic (itchy), purple, polygonal, planar papules and plaques.

Note:

  • Clinically, lichen planus and lichen sclerosus are similar. The main difference is lichen planus involves mucous membranes.[13]

Gross

  • Wickham striae = white lines/dots.
    • Due to hypergranulosis.

Microscopic

Features:[14][15]

  • Loss of basal cells (stratum basale) -- key feature.
  • Loss of rete ridges/formation of pointed rete ridges "sawtoothing".
  • Interface dermatitis (lymphocytes at dermal-epidermal junction).
  • Hypergranulosis; stratum granulosum thickened (grossly seen as "Wickham stria" = white lines).
  • Hyperkeratosis; stratum corneum thickened.
  • Necrotic basal cell in dermis = colloid bodies = Civatte bodies.[16]
    • Pink bodies approximately the size of a keratinocyte.

Notes:

DDx:

Images

  • Lichen planus - intermed. mag. (WC/Nephron)

  • Lichen planus - low mag. (WC/Nephron)

Stains

  • PAS-D or PAS-F to exclude a fungal infection.

Sign out

FORESKIN, CIRCUMCISION:
- LICHEN PLANUS.

VULVA, LEFT POSTERIOR FOURCHETTE, BIOPSY:
- COMPATIBLE WITH LICHEN PLANUS.

Micro

The sections show skin with a lymphoplasmacytic interface dermatitis, basal cell loss, hypergranulosis, hyperkeratosis, loss of the rete ridges and Civatte bodies.

The epidermis matures to the surface. No significant nuclear atypia is identified.

Fungal organisms are not identified with a PAS-D stain.

Lichen sclerosus

Main article: Lichen sclerosus

Microscopic

Features:[19]

  • Subepithelial fibrosis - key feature.

Psoriasis

General

  • Other considerations:
    • Drug-induced psoriasis.[22]

Clinical

  • Auspitz sign = pin-point bleeding on removal of scale.
  • Koebner phenomenon = lesions form at site of trauma.

Common locations:[20]

  • Knees, elbows, scalp, glans penis.

Microscopic

Features:[20]

  • "Regular" acanthosis + long rete ridges (psoriasiform hyperplasia).
  • Parakeratosis.
  • Dilated vessels in superficial dermis (give rise to Auspitz sign).
  • Spongiform pustules = PMNs in stratum spinosum.
  • PMNs in parakeratotic stratum corneum (Munro microabscess).
  • Thinning of the suprapapillary plate.
    • The epidermis between rete ridges is thinner than in the normal adjacent skin - key feature.

DDx:

Note:

Images

www:

Stains

Sign out

SKIN LESION, LEFT ARM, PUNCH BIOPSY:
- SKIN WITH ACANTHOSIS, HYPERKERATOSIS, FOCAL PARAKERATOSIS, PROMINENT
  DILATED VESSELS IN THE SUPERFICIAL DERMIS, SUPERFICIAL SPONGIFORM PUSTULES.
- MILD NONSPECIFIC PERIVASCULAR INFLAMMATION.
- NEGATIVE FOR FUNGAL ORGANISMS WITH PAS STAINING.

COMMENT:
The findings are compatible with psoriasis.

Micro

The sections show skin with regular psoriasiform change, hyperkeratosis, focal parakeratosis, prominent dilated vessels in the superficial dermis, superficial clusters of intraepidermal neutrophils (spongiform pustules) and thinning of the suprapapillary plate is present. A few perivascular inflammatory cells are present.

There is no epidermal necrosis. Eosinophils are not apparent. The lymphocytes do not have significant atypia.

Lichen striatus

General

Features:[24]

  • Benign, self-limited.

Clinical:

Clinical image:

Microscopic

Features:

  • "Ball and glove" pattern:
    • Rete ridges (glove) surround nexts of lymphocytes (ball).
  • Hyperkeratosis.
  • Parakeratosis.

DDx:

Images:

Lichen aureus

General

  • Rare.

Clinical:[25]

  • Plaques + minimal scale - erythematous/golden.

Microscopic

Features:[25]

  • Lymphocyte-predominant perivascular pattern.
    • May have features suggestive of vacuolar interface pattern.
  • Fibrosis of superficial papillary dermis.

Images:

Granuloma faciale

General

Microscopic

Features:[27]

  • Neutrophilic vasculitis - often subtle:
    • Neutrophils within blood vessel walls.
    • Vessels destruction (fibrinoid necrosis or nuclear dust).
  • Mixed inflammatory superficial dermal infiltrate.
    • Eosinophils, neutrophils, plasma cells, histiocytes.
  • Lesion separated from the (normal) epidermis (Grenz zone).[26]

DDx of chronic fibrosing leukocytoclastic vasculitis:[27]

  • Granuloma faciale.
  • Erythema elevatum diutinum - lacks Grenz zone.
  • Inflammatory pseudotumour.

Image:

Atopic dermatitis

  • AKA atopic eczema, AKA infantile eczema.

General

  • Very common - especially in children.[28]
    • Most children outgrow the condition.

Microscopic

Features:

  • Spongiotic dermatitis.

DDx:

Images

  • Mild spongiotic dermatitis - high mag. (WC)

  • Mild spongiotic dermatitis - very high mag. (WC)

Sweet syndrome

General

  • Uncommon.

Microscopic

Features:

  • Nodular and diffuse pattern - neutrophils predominant - without pus.

DDx rips:

Image:

Granuloma inguinale

Not to be confused with granuloma annulare.
  • Previously known as donovanosis.

General

  • Infection caused by Klebsiella granulomatis - Gram-negative, rod-shaped bacteria.
    • Used to be known as Calymmatobacterium granulomatis.[30]

Location:

Clinical:[31]

  • Sexually transmitted.
  • Nodule or papule developing into a painless ulcer in the inguinal region.
  • No lymphadenopathy (unlike syphilis).

Microscopic

Features:

  • Donovan bodies - key feature:
    • Rod-shaped bodies within histiocytes.

DDx:

Image:

Stains

Pyoderma gangrenosum

Main article: Pyoderma gangrenosum

Necrobiotic xanthogranuloma

  • Abbreviated NXG.
Main article: Necrobiotic xanthogranuloma

DDx for pattern

Spongiotic dermatitides

DDx:[1]

Psoriasiform dermatitides

Regular psoriasiform dermatitis

DDx:[1]

Irregular psoriasiform dermatitis

Interface dermatitides

Vacuolar interface dermatitides

DDx:[1]

Others:[1]

Additional:[32]

  • Phototoxic dermatitis.
  • Acute radiation dermatitis.
  • Erythema multiforme-like drug eruption.
  • Lichen sclerosis et atrophicus.
  • Erythema dyschromicum perstans (ashy dermatosis).

Super lame mnemonic Danny G & SLE:

  • Dermatomyositis, GVHD, SLE, Lichen sclerosus, Erythema multiforme.

Lichenoid interface dermatitides

DDx:[1]

Additional:[32]

Bullous disease

Main article: Bullous disease

Subcorneal bullous disorders

DDx with acantholysis:[1]

DDx without acantholysis:DDx:[1]

Suprabasilar bullous disorders

DDx:[1]

Memory device - PhD + Grover = Pemphigus vulgaris, Hailey-Hailey, Darier, Grover.

Subepidermal bullous disorders

DDx:[1]

Others:

Mnemonic DELPHI:

  • Dermatitis herpetiformis.
  • Epidermolysis bullosa acquisita.
  • Bullous lupus erythematosis.
  • Pemphigoid, bullous.
  • Herpes gestationis - rare autoimmune bullous dermatosis of pregnancy, not related to HSV.[33]
  • Linear IgA disease.

Dermatitides with perivascular inflammation

Lymphocytes

Lymphocytes (tightly cuffed):[1]

  • Infections.
  • Medications.
  • Malignancy.
  • Vitiligo (with absent melanocytes).
  • Scleroderma/morphea.

Lymphocytes & plasma cells +/-eosinophils:

  • Erythema chronicum migrans (Lyme disease).

Lymphocytes (not tightly cuffed):

  • Viral exanthems.
  • Drug eruptions.

Lymphocytes & eosinophils:

  • Drug reaction.
  • Insect bite.
  • Dermatophyte infection.

A simple memory device - 6 Ls:[34]

  • Lymphoma.
  • Pseudolymphoma (cutaneous lymphoid hyperplasia, lymphocytoma cutis).
  • Lupus erythematosus.
  • Lymphocytic infiltrate of Jessner / tumid lupus erythematosus.
  • Polymorphous light eruption.
  • Lyme disease.

Neutrophils

DDx:[1]

  • Cellulitis.
  • Neutrophilic eccrine hidradenitis (idiopathic palmar-plantar hidradenitis)

With eosinophils:

  • Urticaria.

Eosinophils

DDx:[1]

  • Hypersensitivity reaction/drug reaction.
  • Insect bite.
  • Bullous pemphigoid, urticarial.

Mast cells

Vasculitis

Main article: Vasculitides

General DDx:

  • Infection.
  • Autoimmune.
  • Malignancy.
  • Toxic (medications).

Small vessel:

Medium vessel:

Medium vessels often with small vessel involvement:

Large vessel:

Nodular and diffuse dermatitides

Neutrophils

With pus (suppurative)

Neutrophils only:

  • Follicular occlusion triad.
  • Ruptured cyst/follicle.

Neutrophils and eosinophils:

  • Halogenoderma.
  • Blastomycosis-like pyoderma (pyoderma vegetans) - due to bacterial infection, usu. S. aureus.

Without pus

With vasculitis:

Without vasculitis:

Lymphocytes

Plasma cells

Eosinophils

Histiocytes

Granulomatous

Sarcoidal
  • Sarcoidosis - have few lymphoid cells around them; thus called "naked granulomas".[2]
Tuberculoid
Foreign body-type granulomas
Palisaded granumolas

Blue granuloma:

Red granuloma:

See also

References

  1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 Brinster NK (March 2008). "Dermatopathology for the surgical pathologist: a pattern based approach to the diagnosis of inflammatory skin disorders (part I)". Adv Anat Pathol 15 (2): 76–96. doi:10.1097/PAP.0b013e3181664e8d. PMID 18418089.
  2. ↑ 2.0 2.1 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.
  3. ↑ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1191. ISBN 978-1416031215.
  4. ↑ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1191. ISBN 978-1416031215.
  5. ↑ JAH. 20 February 2009.
  6. ↑ Crowson AN, Magro CM, Mihm MC (April 2008). "Interface dermatitis". Arch. Pathol. Lab. Med. 132 (4): 652–66. PMID 18384217. http://www.archivesofpathology.org/doi/full/10.1043/1543-2165%282008%29132%5B652%3AID%5D2.0.CO%3B2.
  7. ↑ URL: http://www.dermpedia.org/baby-dermpedia-for-beginners/discoid-lupus-erythematosus. Accessed on: 7 March 2012.
  8. ↑ Chen YJ, Wu CY, Huang YL, Wang CB, Shen JL, Chang YT (2010). "Cancer risks of dermatomyositis and polymyositis: a nationwide cohort study in Taiwan". Arthritis Res. Ther. 12 (2): R70. doi:10.1186/ar2987. PMC 2888225. PMID 20398365. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2888225/.
  9. ↑ Teichman, JM.; Sea, J.; Thompson, IM.; Elston, DM. (Jan 2010). "Noninfectious penile lesions.". Am Fam Physician 81 (2): 167-74. PMID 20082512.
  10. ↑ Gupta, R.; Bansal, B.; Singh, S.; Yadav, I.; Gupta, K.; Kudesia, M. (2009). "Lichen planus of uterine cervix - the first report of a novel site of occurrence: a case report.". Cases J 2: 9306. doi:10.1186/1757-1626-2-9306. PMID 20062629.
  11. ↑ URL: http://emedicine.medscape.com/article/1078327-overview. Accessed on: 11 September 2010.
  12. ↑ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1191. ISBN 978-1416031215.
  13. ↑ McPherson, T.; Cooper, S.. "Vulval lichen sclerosus and lichen planus.". Dermatol Ther 23 (5): 523-32. doi:10.1111/j.1529-8019.2010.01355.x. PMID 20868406.
  14. ↑ URL: http://emedicine.medscape.com/article/1078327-overview. Accessed on: 11 September 2010.
  15. ↑ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Aster, Jon (2009). Robbins and Cotran pathologic basis of disease (8th ed.). Elsevier Saunders. pp. 1192. ISBN 978-1416031215.
  16. ↑ 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. 604. ISBN 978-1416054542.
  17. ↑ URL: http://www.careforumwales.org/cell-carcinoma/histopathologic-terminology.html. Accessed on: 28 August 2011.
  18. ↑ Busam, Klaus J. (2009). Dermatopathology: A Volume in the Foundations in Diagnostic Pathology Series (1st ed.). Saunders. pp. 36. ISBN 978-0443066542.
  19. ↑ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 1065-6. ISBN 0-7216-0187-1.
  20. ↑ 20.0 20.1 20.2 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. 603. ISBN 978-1416054542.
  21. ↑ URL: http://medical-dictionary.thefreedictionary.com/spondylosis. Accessed on: 28 August 2011.
  22. ↑ Milavec-Puretić, V.; Mance, M.; Ceović, R.; Lipozenčić, J. (Mar 2011). "Drug induced psoriasis.". Acta Dermatovenerol Croat 19 (1): 39-42. PMID 21489366.
  23. ↑ URL: http://missinglink.ucsf.edu/lm/dermatologyglossary/psoriasis.html. Accessed on: 4 September 2013.
  24. ↑ 24.0 24.1 Taniguchi Abagge, K.; Parolin Marinoni, L.; Giraldi, S.; Carvalho, VO.; de Oliveira Santini, C.; Favre, H.. "Lichen striatus: description of 89 cases in children.". Pediatr Dermatol 21 (4): 440-3. doi:10.1111/j.0736-8046.2004.21403.x. PMID 15283785.
  25. ↑ 25.0 25.1 Hazan, C.; Fangman, B.; Cohen, D. (2007). "Lichen aureus.". Dermatol Online J 13 (1): 23. PMID 17511956.
  26. ↑ 26.0 26.1 URL: http://dermatlas.med.jhmi.edu/derm/indexDisplay.cfm?ImageID=1289066309. Accessed on: 23 September 2011.
  27. ↑ 27.0 27.1 Busam, Klaus J. (2009). Dermatopathology: A Volume in the Foundations in Diagnostic Pathology Series (1st ed.). Saunders. pp. 198-9. ISBN 978-0443066542.
  28. ↑ URL: http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001856/. Accessed on: 28 December 2011.
  29. ↑ URL: http://dermatology.cdlib.org/94/NYU/Apr2002/7.html. Accessed on: 4 January 2012.
  30. ↑ O'Farrell N (December 2002). "Donovanosis". Sex Transm Infect 78 (6): 452–7. PMC 1758360. PMID 12473810. http://sti.bmj.com/cgi/pmidlookup?view=long&pmid=12473810.
  31. ↑ Bezerra, SM.; Jardim, MM.; Silva, VB. (Jun 2011). "Granuloma inguinale (Donovanosis).". An Bras Dermatol 86 (3): 585-6. PMID 21738983.
  32. ↑ 32.0 32.1 Alsaad, KO.; Ghazarian, D. (Dec 2005). "My approach to superficial inflammatory dermatoses.". J Clin Pathol 58 (12): 1233-41. doi:10.1136/jcp.2005.027151. PMC 1770784. PMID 16311340. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770784/.
  33. ↑ URL: http://emedicine.medscape.com/article/1063499-overview. Accessed on: 23 September 2011.
  34. ↑ URL: http://www.dermpathmd.com/mnemonics/mnemonics_dermatopathology.htm. Accessed on: 23 September 2011.

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