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23 Cards in this Set
- Front
- Back
Rosacea stages
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-Blood flow is higher than in normal skin.
-1: Pre-rosacea: episodic flushing of the central portion of the face. -2: Vascular rosacea: Recurrent, maybe painful blush on nasal ala/cheeks. -3: Inflammatory rosacea: Small papules and pustules, deeper red than acne, persistent inflammation. -4: Sebaceous hyperplasia and phymatous rosacea: Overgrowth of sebaceous glands. |
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Pemphigus vulgaris
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Lethal, peaks at 30-50
Painful blistering MHC Class II genes associated: DR4 in Ashkenazi Jews, DQ1 in others. No real inflammation Desmoglein 3 and 1 are targeted. Treat with prednisone and human immunoglobulins. |
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Bullous pemphigoid
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Non-lethal, peaks at 60-80 years.
Painless, pruritic blisters. ABs against BP180 epitope of hemidesmosome Inflammatory Treat with anti-inflammatory drugs |
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Psoriasis
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Th1 cytokines (autoimmunity): TNFa, IFNgamma, IL-2
HLA subtype Cw13 confers increased RR. White, silvery scales. Treat with topical treatments, phototherapy, immunosuppressives. |
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Atopic dermatitis
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Th2 cytokines: IL-4,5,6,9,10,13
Goes with allergies Patients have pruritis and eczema. Can lead to cutaneous infections like impetigo and s. aureus. |
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Moles:
Junctional: Compound: Intradermal: |
Junctional: Symmetric, flat, no melanocytes within dermis.
Compound: Raised, maybe hairy, melanocytic nests within dermis. Intradermal: Raised, skin-colored, with no melanocytes in epidermis. |
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ABCDEs of evaluating melanoma
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Asymmetry
Border (irregular?) Color (uneven?) Diameter (>5mm?) Evolution (changing?) |
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Rates and deaths from melanomas and basal cell carcinomas
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BCC: 80% of new skin cancers.
Melanomas: 80% of skin cancer deaths. |
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Basal cell carcinomas
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Mutations in hedgehog pathways.
Tend not to metastasize, but aggressive locally. Waxy, pearly. |
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Squamous cell carcinomas
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Mutations in p53 suppressor gene.
Erythmatous, scaly. More metastases than BCCs, but still relatively low risk. Actinic keratosis is a precursor lesion. |
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Order corticosteroids from weakest to strongest
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Hydrocortisone < triamcinalone < fluocinonide (Lidex) < Clobetasol (Tmeovate, strongest).
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Differences between "pigmented" skin and "unpigmented" skin
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Black skin is = SPF 13.
More dilated blood and lymphatic vessels in black skin. Multinucleate fibroblasts in black skin. Black hair tends to be elliptical and small on x-section with a curved follicle. White hair tends to be round, medium diameter, and straight or curled follicle. |
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Brown birthmark in baby
Diagnostic criteria |
Example: Neurofibromatosis Type I
>2 Neurofibromas Freckling in axilla or groin. > 6 Cafe au lait spots Optic glioma >2 Lisch nodules Sphenoid or long bone dysplasia Relative with NF1. |
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White birthmark in baby
Diagnostic criteria |
Example: Tuberous sclerosis.
Neurologic impairment (seizures), multisystem hamartomas, hypopigmented macules and angiofibromas. In _neonates_ or _fetuses_ you see cardiac rhabdomyomas. In _infants_ you see hypomelanotic macules. In _teenagers_ you see angiofibromas, etc. Renal disease most common cause of death. |
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Red birthmark in baby
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Example: Infantile hemangioma.
4-10% of white infants, female preponderance, prematurity is a risk factor. watch out for PHACE(S) syndrome. Treat with systemic steroids or propanolol. |
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Yellow birthmark in baby
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Example: Nevus sebaceous.
1/300 newborns, present with small immature sebaceous glands. Small risk of tumors arising. |
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Retinoid nomenclature:
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Vitamin A = all-trans retinol, an alcohol.
Beta carotene is cleaved into 2 Vitamin A's. All-trans retinaldehyde is formed by oxidation of Vitamin A. All-trans retinoic acid = Tretinoin, binds RAR receptor (86%). An isomer of retinoic acid binds RXR (14%). All retinoids increase collagen synthesis. CYP450 hydroxylates retinoic acid to eliminate it. |
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Non-blistering drug eruptions
Exanthematous/morbilliform: Erythema: Urticarial: |
Exanthematous/morbilliform: Most common, pink, red, macules or papules. Sometimes begins > 1 week post-exposure. Drug-induced hyerpensitivity CAN BE FATAL! (Bactrim)!
Erythema: Hypersensitivity reaction to rapidly infused Vancomycin. Urticarial: Wheal, type 1 IgE mediated hypersensitivity reaction. PCN and derivatives, ACE inhibitors, aminoglycosides, etc. |
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Blistering drug eruptions
Fixed drug eruption: Stevens-Johnson Syndrome: Toxic epidermal necrolysis: Acute Generalized Exanthematous Pustulosis: |
Fixed drug eruption: Sharply demarcated, round, dusky erythematous plaques. Recur at same anatomic site with repeat exposure.
Stevens-Johnson Syndrome: Fever, mucous membrane erosions, "target" shaped lesions. Less than 10% of body and 5% mortality. Toxic epidermal necrolysis: Like SJS but > 30% of body surface and 30-50% mortality. Acute Generalized Exanthematous Pustulosis: Acute pustular eruption, comes on quickly and resolves quickly. Macrolides, PCN, etc. |
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Cutaneous manifestations of internal diseases:
Paraneoplastic pemphigus (PNP): Neutrophilic dermatosis: |
Paraneoplastic pemphigus (PNP): Severe mucosal ulceration. Similar to pemphigus vulgaris but with different immunoprecipitation charateristics.
Neutrophilic dermatosis: Rapidly expanding painful, ulcerative lesions. Can get worse after debridement! |
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Cutaneous manifestations of internal diseases (GI disorders):
Peutz Jeghers: Acrodermatitis enteropathica: Glucagonoma syndrome (migratory necrolytic anemia): |
Peutz Jeghers: Hereditary polyposis with hyperpigmented macules.
Acrodermatitis enteropathica: Zinc absorption disorder, presents at infancy with dermatitis, alopecia, diarrhea. Glucagonoma syndrome (migratory necrolytic anemia):Due to excessive glucagon production by pancreatic tumor. |
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Cutaneous manifestations of internal diseases (endocrine/metabolic):
Necrobiosis Lipoidica diabeticorum: Pretibial myxedema: Acanthosis Nigricans: |
Necrobiosis Lipoidica diabeticorum: Well-demarcated plaques on front of lower legs in diabetics or patients with poor glucose tolerance.
Pretibial myxedema:Indurated flesh-colored plaques seen in hyperthyroidism of Grave's disease. Acanthosis Nigricans: Velvety thickening and hyperpigmentation in diabetics/glucose intolerants. |
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Common skin infections:
Bacterial diseases: Viral diseases: Fungal diseases: |
Bacterial diseases:Strep (impetigo, erysipelas, cellulitis), staph (folliculitis, furuncles, carbuncles)
Viral diseases: DNA viruses (papova, poxviridae (molluscum), herpesvirus. Fungal diseases: Malessezia furfur (tinea versicolor), candida albicans (thrush, antertrigo, angular cheilitis). |