Non-neoplastic skin Flashcards
(40 cards)
acute inflammatory dermatosis with spongiosis and formation of intraepidermal vesicles

Acute Eczematous Dermatosis (Eczema)
oozing/ crusted erythematous papulovesicular lesion with pruritic scaling plaques
Eczema
Self limiting Type 4 hypersensitive acute inflammatory dermatosis with keratinocyte injury mediated by CD8+ T cells

Erythema Multiforme
Causes of erythema multiforme
Infection
- HSV
- Histoplasma
- Coccidiomycosis
- Typhoid
- Leprosy
Drugs
- Sulfa
- Penicillins
- Barbiturates
- Salicylates
- Hydantoins
- Anti-malarials
SLE
Polyarteritis nodosa
Dermatomyositis
Immunizations
- Erythematous maculopapular rash, progressing into target lesions
- Pruritic or burning sensations
- symmetrical distribution to dorsal hands and feet, followed by proximal spread
- can include palms and soles
- only in major case will mucocutaneous surfaces be affected
Clinical Presentation of Erythema Multiforme

What is the difference between Stevens-Johnson Syndrome and TEN?
SJS is less than 10% of total body surface
TEN includes > 30% of the body’s surface

Leukopenia
increased BUN
Increased transaminases
Hyperglycemia
subepidermal splitting at dermo-epidermal junction
Diagnostics of SJS/ TEN
Infections
- CMV
- Herpes
- Mycoplasma
Drugs
- Sulfa
- Aminopenicillins
- Rifampin
- Corticosteroids
- Nevirapine
- Antiepileptics
- Piroxicam
- Allopurinol
Vaccinations
Graft vs Host Disease
Triggers of SJS/ TEN
Prodromal Phase
ALWAYS has Mucocutaneous Manifestations
Positive Nikolsky sign
Necrosis and sloughing of full epidermal thickness
Involves face and trunk
Lesions form bullae/ vesicles
Clinical Presentation of SJS/ TEN
Chronic inflammatory dermatosis with sensitized CD4+ T cells causing keratinocyte death by CD8+ T cells
Leads to hyperkeratosis
Psoriasis Pathology
Associations of Psoriasis
arthritis
myopathy
enteropathy
staph/ strep infections
mechanical irritation
Drugs (beta-blockers, chloroquine, lithium, interferon)
HLA-Cw
Diagnostics of Psoriasis
positive Auspitz sign
increased inflammatory markers
stratum corneum cells still have nuclei
increased stratum corneum
decreased stratum granulosum
What is an Auspitz sign
small pinpoint bleeding that occurs when scaled skin is scraped off
Acanthosis
Parakeratosis
Munro microabscesses
Psoriasis Morphology
Well demarcated pink plaques covered by loosely adherent silver scales
primarily appears in extensor surfaces
pruritis
Koebner phenomenon
Positive Auspitz sign
Psoriasis

acanthosis
epidermal hyperplasia
Wickham’s striae
pattern of white lines on lesion surface
Koebner Phenomenon
physical stimuli leading to skin lesions typical of underlying condition on previously healthy skin
oily skin
stress
androgenic alopecia
immunodeficiency
familial history
increased sebum production
Malassezia furfur
Associations of seborrheic dermatitis
Erythematous plaques with patchy scaling and greasy yellow crusting
usually distributed along areas of hair and oily skin
dandruff
pruritis/ burning sensations
originates in the dermis
Clinical presentation of seborrheic dermatitis
Pathology of seborrheic dermatitis
increased sebum production and colonization of yeasts in sebaceous areas or exposure to irritants
Chronic, but Self-limited CD8+ immune response associated with Hep C
Lichen Planus
Diagnostics of Lichen Planus
Wickham’s striae
Band-like lymphocytes at dermo-epidermal junction
irregular saw tooth acanthosis
hyperkeratosis
wedge-shaped hypergranulosis
Purple, pruritic, planar, polygonal, papules and plaques of the skin and mucosa
involves stratum corneum and granulosum
Lichen planus





