Skin pathology Flashcards
1
Q
Atopic dermatitis
A
- Pruritic, erythematous, oozing rash with vesicles and edema
- Often involves face and flexor surfaces
- Type I HSR, associated wit asthma and allergic rhinitis
2
Q
Contact dermatitis
A
- Pruritic, erythematous, oozing rash with vesicles and edema
- Arises upon exposure to allergens
- Irritants: poison ivy and nickel jewelry (type IV HSR), irritant chemicals (e.g., detergents), drugs (e.g., PCN)
- Treatment: removal of offending agent, topical steroids, if needed
3
Q
Acne vulgaris
A
- Comedones (whiteheads and blackheads)
- Pustules (pimples)
- Nodules
- Due to chronic inflammation of hair follicles and sebaceous glands
- Hormone-related increase in sebum and excess keratin block follicles (comedones)
- Propionibacterium acnes infection leads to inflammation (pustules or nodules)
- Treatment: benzoyl peroxide
4
Q
Psoriasis
A
- Well-circumscribed salmon-colored plaques with silvery scale. Ausspitz sign
- Usually on extensor surfaces of elbows and knees, as well as the scalp and sacral area
- Due to excessive keratinocyte proliferation
- Possible autoimmune etiology
- Associated wit HLA-C allele on PSORS1 on chromosome 6
- 30% - facility history, HLA B13, 17
- Lesions often arises in areas of trauma (environmental trigger)
- Treatment: corticosteroids, UVA-light with psoralen, immune-modulating therapy
5
Q
Varicella (chickenpox)
A
- Viral infection of childhood
- Characterized by fever and a generalized vesicular eruption
- The varicella-zoster virus may remain latent for years in dorsal root ganglia
6
Q
Pemphigus vulgaris
A
- Autoimmune destruction of desmosomes
- Formation of severe intraepidermal bullae is characteristic
- First lesions often occur in the oral mucosa, and extensive skin involvement follows
- Due to IgG antibody against desmoglein
- IF highlights IgG surrounding keratinocytes (‘fish net’)
- Rupture easily - leaving large denuded surfaces subject to secondary infection
7
Q
Lichen planus
A
- Pruritic, planar, polygonal, purple papules
- Often with reticular white lines on surface (Wickham striae)
- Commonly involves wrists, elbows, and oral mucosa
- Inflammatory infiltrate composed of lymphocytes at the dermal-epidermal junction (‘saw-tooth’ appearance)
- Presence of apoptotic keratinocytes mainly in basal cell layer
- Etiology is unknown - associated with chronic hepatitis C virus infection and vaccination against hepatitis
8
Q
Bullous pemphigoid
A
- Resembles pemphigus vulgaris, but is much less severe
- Autoimmune destruction of hemidesmosome
- IgG autoantibodies agianst epidermal BM
- Presents as subepidermal blisters of skin filled with fluid containing eosinophils (between dermis and epidermis); oral mucosa is spared
- Tense bullae do not rupture easily
9
Q
Dermatitis herpetiformis
A
- Due to autoimmune deposition of IgA at tips of dermal papillae
- Presents as pruritic vesicles and bullae that are grouped
- Usually involves the extensor surfaces of the knees and elbows, scalp, upper back, and sacral area
- Dermal microabscesses with neutrophils and eosinophils at the tips of dermal papillae
- Associated with celiac disease
- Resolve with a gluten-free diet
10
Q
Erythema multiforme
A
- Presents with multiple type of lesions, including macules, papules, and vesicles
- Characteristically associated with a ‘target’ lesion resembling an archer’s bull’s eye
- Most commonly associated with HSV infection
- Usually hypersensitivity to coexistent infectious agents, various drugs, a concomitant connective tissue disorder, or an associated malignancy
- EM variants: Stevens-Johnson syndrome, Toxic epidermal necrolysis
11
Q
Vitiligo
A
- Localized loss of pigmentation
- Due to autoimmune destruction of melanocytes by toxic intermediates of melanin production or by neurochemical factors
- Associated with autoimmune disorders, such as Graves disease and Addison disease
12
Q
Albinism
A
- Congenital lack of pigmentation
(1) Ocular albinism: melanin dysfunction limited to the eyes; X-linked disorder
(2) Oculocutaneous albinism: involves eyes, skin, and hair; predisposes to actinic keratosis, basal and squamous cell carcinoma, and malignant melanoma; most often autosomal recessive - Tyrosine-negative albinism - failure of conversion of tyrosine to DOPA
- Tyrosine-positive albinism - unknown etiology
13
Q
Freckle
A
- Increase of melanin pigment within basal keratinocytes - melanosomes
- Darkens when exposed to sunlight
14
Q
Lentigo
A
- Pigmented macule caused by melanocytic hyperplasia in the epidermis
15
Q
Melanocytic nevus
A
- Lesion classified as a benign tumor or hamartoma
- Nevus cells are derived from melanocytes and ordinarily occur in cluster or nests
(1) Juntional nevus: confined to the epidermal-dermal junction, most common mole in children
(2) Compound nevus: both at the epidermal-dermal junction and in the dermis
(3) Intradermal nevus: cinfined to clusters within the dermis, most common mole in adults