Difference between revisions of "Inflammatory skin disorders"
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*Linear rash usu. on lower extremity. | *Linear rash usu. on lower extremity. | ||
*Associated with atopy, [[lichen sclerosus]].<ref name=pmid15283785/> | *Associated with atopy, [[lichen sclerosus]].<ref name=pmid15283785/> | ||
*Children. | |||
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*"Ball and glove" pattern: | *"Ball and glove" pattern: | ||
**Rete ridges (glove) surround nexts of lymphocytes (ball). | **Rete ridges (glove) surround nexts of lymphocytes (ball). | ||
*Hyperkeratosis. | |||
*Parakeratosis. | |||
Images: | Images: | ||
Revision as of 17:53, 22 September 2011
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.
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 |
(WC) |
| Interface | inflammation at DE junction | -vacuolar (minimal) -lichenoid (band-like) |
-erythema multiforme, SLE -lichen planus |
|
| 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 |
(WC) |
| Spongiotic | small empty spaces between keratinocytes; quasi-microvacuolar appearance | -acute -subacute -chronic |
-poison ivy -nummular dermatitis -atopic dermatitis |
(WC) |
| Vasculitis | inflammation of vessel wall/vessel was destruction | -small vessel -medium vessel -large vessel |
-leukocytoclastic vasculitis -PAN -giant cell arteritis |
(WC) |
| Perivascular | inflammation around vessels | -neutrophilic -lymphocytic -mastocytic -eosinophilic |
-cellulitis -viral exanthem, Rx reaction -mastocytosis -insect bite, Rx reaction |
(WC) |
| Panniculitis | inflammation of adipose tissue | -septal -nodular |
-erythema nodosum, scleroderma panniculitis -erythema induratum, infection |
|
| Psoriasiform | epidermal thickening and long rete ridges |
-regular -irregular |
-psoriasis -lichen simplex chronicus |
(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.
- Others.
Microscopic
- 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.
Systemic lupus erythematosus
Main article: Systemic lupus erythematosus
General
- Systemic disease with multi-organ manifestations.
May present with different skin manifestations:
- Panniculitis.
- Vacuolar interface dermatitis.
Microscopic
Features:
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.[7]
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
General
Etiology:
- Autoimmune disease, T-cell–mediated.[10]
Clinical:[11]
- 6 Ps: pruritic (itchy), purple, polygonal, planar papules and plaques.
Gross
- Wickham striae = white lines/dots.
- Due to hypergranulosis.
Microscopic
- 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.[14]
DDx:
- Bullous disease, subepithelial vesicular.
- Lichenoid keratosis - parakeratosis prominent.
Notes:
- Hyperkeratosis and hypergranulosis are not seen in erythema multiforme.
- Colloid bodies = cytoid bodies = Civatte bodies = hyaline bodies = apoptotic bodies.[15]
Images:
Lichen sclerosus
Main article: Lichen sclerosus
Microscopic
Features:[16]
- Subepithelial fibrosis - key feature.
Psoriasis
General
- Chronic skin condition +/- systemic involvement:[17]
- Arthritis.
- Myopathy.
- Enteropathy, e.g. inflammatory bowel disease.
- Syondylitic joint disease (spondylos = vertebrae[18]).
Clinical:
- Auspitz sign = pin-point bleeding on removal of scale.
- Koebner phenomenon = lesions form at site of trauma.
Microscopic
Features:[17]
- Acanthosis + long rete ridges - key feature.
- 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.
Lichen striatus
General
Features:[19]
- Benign, self-limited.
Clinical:
- Linear rash usu. on lower extremity.
- Associated with atopy, lichen sclerosus.[19]
- Children.
Clinical image:
Microscopic
Features:
- "Ball and glove" pattern:
- Rete ridges (glove) surround nexts of lymphocytes (ball).
- Hyperkeratosis.
- Parakeratosis.
Images:
DDx for pattern
Spongiotic dermatitides
DDx:[1]
- Atopic dermatitis.
- Contact dermatitis.
- Stasis dermatitis.
- Seborrheic dermatitis.
- Nummular dermatitis.
- Spongiotic drug eruption.
Psoriasiform dermatitides
Regular psoriasiform dermatitis
DDx:[1]
- Psoriasis vulgaris.
- Dermatophyte infection.
- Pityriasis rubra pilaris.
Irregular psoriasiform dermatitis
Interface dermatitides
Vacuolar interface dermatitides
DDx:[1]
- Erythema multiforme.
- Lichen sclerosus.
- Fixed drug eruption.
Others:[1]
- Graft versus host disease.
- Dermatomyositis.
- Systemic lupus erythematosus.
- Morbillifrom viral exanthem.
Lichenoid interface dermatitides
DDx:[1]
- Lichen planus
- Mycosis fungoides.
- Discoid lupus erythematosus.
- Lichenoid drug eruption.
- Fixed drug eruption.
Bullous disease
Main article: Bullous disease
Subcorneal bullous disorders
DDx with acantholysis:[1]
DDx without acantholysis:DDx:[1]
- Subcorneal pustular dermatosis (Sneddon-Wilkinson disease)
- Pustular psoriasis.
- Pustular drug eruption (acute generalized exanthematous pustulosis).
Suprabasilar bullous disorders
DDx:[1]
- Pemphigus vulgaris.
- Hailey-Hailey disease (benign familial pemphigus).
- Darier disease.
- Grover disease (transient acantholytic dermatosis).
Subepidermal bullous disorders
DDx:[1]
- Bullous pemphigoid.
- Cicatricial pemphigoid.
- Porphyria cutanea tarda.
- Epidermolysis bullosa acquista.
- Dermatitis herpetiformsis.
- Linear IgA disease.
Others:
- Insect bite.
- Coma blister.
- Bullous systemic lupus erythematosus.
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.
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:
- Churg-Strauss syndrome.
- Microscopic polyangiitis.
- Mixed cryoglobulinemia.
- Connective tissue diseases.
Large vessel:
Nodular and diffuse
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 neutrophilic dermatoitis.
- Bowel-associated ermatosis-arthritis syndrome.
Lymphocytes
- Reactive lymphoid hyperplasia - may be due to drugs.
- Lymphoid malignancy.
Plasma cells
- Inflammation.
- Plasma cell neoplasms.
- 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".[2]
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
References
- ↑ 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.
- ↑ 2.0 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.
- ↑ 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.
- ↑ 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.
- ↑ JAH. 20 February 2009.
- ↑ 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.
- ↑ 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/.
- ↑ Teichman, JM.; Sea, J.; Thompson, IM.; Elston, DM. (Jan 2010). "Noninfectious penile lesions.". Am Fam Physician 81 (2): 167-74. PMID 20082512.
- ↑ 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.
- ↑ URL: http://emedicine.medscape.com/article/1078327-overview. Accessed on: 11 September 2010.
- ↑ 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.
- ↑ URL: http://emedicine.medscape.com/article/1078327-overview. Accessed on: 11 September 2010.
- ↑ 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.
- ↑ 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.
- ↑ URL: http://www.careforumwales.org/cell-carcinoma/histopathologic-terminology.html. Accessed on: 28 August 2011.
- ↑ 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.
- ↑ 17.0 17.1 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. 603. ISBN 978-1416054542.
- ↑ URL: http://medical-dictionary.thefreedictionary.com/spondylosis. Accessed on: 28 August 2011.
- ↑ 19.0 19.1 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.