Epidermis and Dermis Flashcards
1
Q
Layers of the epidermis (top to bottom)
A
- Stratum corneum
- Stratum lucidum (only in palmar and plantar skin)
- Stratum granulosum
- Stratum spinosum
- Stratum basale
2
Q
Basal cell carcinoma
A
- Most common CA, highest rates in caucasians
- Risk factors: fair skin, UV light
- Location is usually head/neck
- Pearly papule forms, often bleeds
3
Q
Melanoma Dx
A
- ABCDE’s
- Asymmetry of the spot
- Border irregularity
- Color variation/change
- Diameter change
- Evolution
4
Q
SCC
A
- 2 groups: aggressive or non-aggressive
- Aggressive: prior radiation, thermal injury, chronic draining sinuses, chronic ulcers, immunosuppression
- Non-aggressive: sun exposure
5
Q
Dandruff
A
-Due to inflammation in the stratum granulosum/stratum corneum (superficial layers)
6
Q
Skin collagen
A
- Most skin collagen is type I (reticular dermis)
- Type III around the papillary dermis
- Type IV in basement membrane
7
Q
Layers of the basement membrane zone (BMZ)
A
- Separates epidermis from dermis
- Basal keratinocytes
- Lamina lucida (laminins)
- Lamina densa (type IV collagen)
- Sub-laminar densa fibrillar zone (anchoring fibrils, elastic/micro fibrils, type VII collagen)
8
Q
Genetic epidermolysis bullous (EB) diseases
A
- Genetic defects (mutations)
- EB simplex (keratin 5 + 14), in epidermis (effects basal keratinocytes), leaves intra-epidermal blister
- EB simplex w/ pyloric atresia or muscular dystronphy (plectin), intra-epidermal (effects basal keratinocytes)
- Junctional EB (17 collagen, laminin, integrins), in lamina lucida (sub-epidermal)
- Dystrophic (scarring) EB (type VII collagen, sub-epidermal lesions)
9
Q
Bullous pemphigoid
A
- Autoimmune against type XVII collagen (BP Ag 2), (pathogenic form)
- Results in dysfunctional hemidesmosomes
- Sub-epidermal lesion
- Other forms (non-pathogenic, all in hemidesmosomes): plectin, BP Ag 1, alpha 6 and 4 integrin
10
Q
Lamins
A
- Helps type IV collagen (in lamina densa) bind to keratinocyte, binds to other macromoluecules and cells
- Very adhesive, shaped like a cross
11
Q
Type IV collagen
A
- Highly sulfated domain
- Helical and non-helical (flexible) domains
- Globular carbohydrate domain
12
Q
Proteoglycans
A
- Protein core w/ glycosaminoglycans (GAGs) disaccharides coming off protein
- can be heparan sulfate rich
13
Q
Pemphigus
A
- IgG against desmoglein 3 of desmosomes, keratinocytes disadhere to each other
- Leaves intra-epidermal blister
- Desmoglein 1 found in more superficial layers
14
Q
EBA (Epidermolysis bullosa acquisita)
A
- IgG against type VII collagen
- Leads to sub-epidermal blisters
15
Q
Diseases summary for bullous
A
- Abs against desmoglein 1 or 3 gives rise to pemphigus (intra-epidermis)
- Mutations plectin and keratin gives rise to EB simplex (intra-epidermal)
- Abs against type XVII (BP Ag, in HDs) gives rise to bollus pemphigoid (sub-epidermial)
- Mutations in type 17, laminins, integrins in lamina lucida gives rise to junctional EB (sub-epidermal)
- Abs against laminin 5 (332, lamina lucida) gives rise to MMP/CP (mucous membrane pemphigoid), sub-epidermal
- Abs against type VII (anchoring fibril) gives rise to EBA (sub-epidermal)
- Mutation in type 7 gives rise to dystrophic EB (sub-epidermal)
- IgA Abs against epidermal transglutamase enz gives rise to DH (dermatitis herpetiformis), sub-epidermal lesions
16
Q
Features to look for during skin examination
A
- Distribution (site/extent of involvement, symmetrical, characteristic location)
- Arrangement of multiple lesions (patterns)
- Shape of individual lesion (diffuse vs demarcated)
- Specific type of lesion
17
Q
Describing lesions
A
- Color
- Consistency
- Surface appearance (scaly, crusty, ect)
- Anatomic components of skin affected
- Type of lesion
18
Q
Macule
A
- Circumscribed, flat lesion that differs from surrounding skin by color
- Can be any size or shape
- Can be hypo or hyperpigmented, purport, or erythemetous/telangectasia (difference being redness goes away w/ pressure if erythemetous)