Derm 2.0 Flashcards
What are the two functions of the epidermis?
Where is the epidermis thinnest and thickest?
What are the 5 layers from superficial to deep
Pathogen barrier, Water regulation
0.3mm- eyelid
3mm- back
Corenum- dead cells, primary barrier
Lucidum- lucent, only in thickest skin
Granulosum- keratinocytes lose nuclei/flatten
Spinosum- desmosome connection, Langherhan location
Basal- dividing keratinocytes, melanocyte/Merkel location
What are the 9 examples of primary lesions
MP3 NPV BW
Macule- flat discoloration
Patch- macule >1cm wide
Papule- elevated, < than .5cm wide
Plaque- elevated lesion >0.5cm, made of papules
Nodule- elevated, round lesion >0.5cm (large= tumor)
Pustule- collected leukocyte fluid (pus)
Vesicle- collection of free fluid 0.5cm or <
Bulla- collected fluid >0.5cm
Wheal- edematous plaque from dermis infiltration by fluid
Define Secondary Lesions and what their presence infers
Primary lesion modification (scratching, infection)
Infers primary Dz process
Fissure- loss of epi/dermis w/ defined walls
Atrophy- skin depression from thinning of epi/dermis
Crust- dried serum/cellular debris (scab)
Erosion- loss of epidermis, not below DE junction= no scar
Scale- excess cells from abnormal keratinization/shedding
Ulcer- loss of epidermis and dermis; heal w/ scar
Scar- abnormal CT formation, implies dermal damage
Define Special Skin Lesion
Lesion not characterized by primary or secondary definitions EMC BLT PCP:
Excoriation: linear erosion from scratching
Milia: superficial keratin cyst w/out opening
Comedone: plug in follicle (dilated- black, narrow- white)
Burrow: channel from parasite
Lichenification: thickened epidermis from scratching
Telangiectasia: dilated superficial blood vessel
Petechia: blood deposit <0.5cm wide
Cyst- lesion w/ wall and lumen
Purpura: blood deposit >0.5cm wide
What type of skin test is done for herpes
What is patch testing done for
What are the four main Tx categories of derm
Tzanck prep
Allergies
Topical Systemic Photo-therapy Surgical
What is the purpose of Topical Therapy
Dry skin/cutaneous lesions are corrected by replacing moisture w/ ? two ways
Xerosis Cutis:
Sxs
MC location/worse during ? time
Tx
Restore skin function after removal of water/lipid/protein from epidermis
Emollient cream, Lotion
Rough skin w/ white scale, progress to thick/tan patches
MC: hands/lower legs, worse during dry/winter months
Tx: emollients- 12% lactate lotion (Lac-Hydrin, AmLactin)
Emollient w/ ? two added ingredients have special lube power
? is thicker and more lubricating than lotion
What two ingredients can be added to topical therapies to decrease pruritus
Urea (Carmol, Vanamide) Lactic Acid (Lac-Hydrin, AmLactin)
Creams
Menthol, Phenol
What are 4 solutions used for Topical Therapy: Wet Dressings and indications for use
What is the technique for using Wet Dressings
Silver Nitrate 0.5%- aqueous solution, can stain skin; bactericidal, infected lesions (stasis ulcers/dermatitis)
Water- no need to be sterilized; Sunburn Ivy Non-infected
Acetic acid 1-2.5%- diluted vinegar; Pseudomonas
Burrows (Aluminum Acetate)- 1-3 packets in 16oz water, mild antiseptic; Athlete foot, Bite, Ivy acute inflammation
4-8 layers of material
Wring until sopping wet
Place on area and leave x 30-60min x 2-4/day
Stop when skin becomes dry
Define Vehicle and what does the vehicle determine
What are the 6 types of Vehicles
Base substance that disperses active ingredient
Rate of absorption
Ointment: primarily grease w/out preservatives
Most Moisturizing Occlusive Lipophilic
Not for: acute eczematous inflammation/intertriginous
Cream: organic chemical, water, preservative.
Most useful: intertriginous
Adverse: Sting Allergy Irritate Dryness
Foam: useful for Scalp dermatosis Ivy Plaque psoriasis
Don’t use <12y/o or >2wks
Lotion/Solution: water, ETOH and chemical mixture; LEAST lipophilic/MOST useful on scalp
Adverse: intertriginous use= sting/dryness
Gel: propylene glycol and water/alcohol; Greaseless
Useful: Ivy, Scalp
Waterproofing occlusion can enhance a steroids potency by ? much
Application to ? areas have natural occlusion and need caution
What effect does Hydration have on Topical Steroid Therapy
? regions of the body will have in/decreased topical steroid absorbing abilities
100x
Obese Axilla Inguinal Diaper
Stretches cellular connections- inc absorption 4-5x
Inc: eye lid/face d/t thin corneum w/ inc blood flow
Dec: sole/palm d/t thick stratum corneum
What are the local adverse effects of using Topical Steroid Therapy
WAR BIRD BASHH
Worsening infection
Atrophy
Rebound phenomenom
Burning
Itching
Rosacea
Dry skin d/t cream/lotion
Bruising Acne/folliculitis Striae Hypertrichosis (face) Hypopigmentation
How does local allergic reaction to topical steroid therapy present
Occasionally this allergic reaction will develop ? three signs?
If an allergic reaction is suspected, what is the next step
Chronic dermatitis that isn’t worse/better w/ CCS
Exanthem Purpura Urticaria
Patch testing
What are the adverse systemic effects of Topical Steroid Therapy
What are two benefits of IM steroid therapy and what is the risk of use
FTT Adrenal axis suppression (<2y/o, puberty) Glaucoma Stunted growth Cushing Syndrome Cataracts
Longer lasting, Easier
Local atrophy, especially if needle too short
What are the 5 MC mistakes of Topical Steroid Therapy
What is the unit of measurement for Topical Steroid application and what does this unit of measurement equate to in weight
Define the “Rule of Hand” for Topical Steroid Therapy usage
How much does one hand area equate to
How many hand areas are needed for one gram of medication
Failure to f/u
Too weak
Not enough given
Too strong face/kid
Finger Tip Unit- 5mm diameter
1FTU- 0.5gm
0.5FTU= one hand area/0.25gm
1% TBSA
4 hand areas= 1gm
Face/neck= ? FTU
Trunk= ? FTU
Arm= ? FTU
Hand= ? FTU
Leg= ? FTU
Foot= ? FTU
Child FTU Chart
F/n= 2.5FTU
Front/back trunk= 7FTU
Arm= 3 FTU
Hand= 1FTU
Leg= 6FTU
Foot= 2FTU
Deck 2, Slide 45
Topical Steroid Therapy dosing in general should not exceed ? much Group 1 agent
How often should certain steroid Groups be applied
Define Pulse Therapy and why would it be done w/ Group 1 agents
45-60gm/wk
1: QD-BID
2-6: BID x 2-6wks
2wks on, 1wk off
Avoids tachyphylaxis
? is the MC inflammatory skin Dz
This MC is often referred to as ?
What are the four characteristics of this MC
Eczema
Dermatitis- inflammation of the skin
Pruritus Erythema Vesicles Scale
What are the characteristic PE findings of the 3 stages of Eczema that can occur in any order, etiology and Txs
Acute: Vesicle Itch Bullae Erythema
D/t: Nummular Pompholyx Contact Stasis
Tx: ABX Steroid Antihistamine Cold compress
Subacute: Fissure Erythema Parched Scale
D/t: Atopic Contact Irritant Asteatotic
Tx: Antihistamine Steroids Emollients ABX
Chronic: Lichenification Excoriation Accentuation Fissure
D/t: LSC Atopic Habitual scratching
Tx: Antihistamine Steroid w/ occlusion Emollient ABX
How does Dyshidrotic Eczema present
What c/c may precede any PE finding
This is d/t irritants and is related to ?
How is Dyshidrotic Eczema managed and what is used as last resort when others fail
Symmetric ‘tapioca lesions; on palm/lateral finger/foot
Mod/Sev itching that turns into pain
Atopic dermatitis
PUVA- Psoralen+UV radiation Antihistamine Cool wet compress Steroids w/ occlusion Last Resort: Low dose Methotrexate
Define Asteatotic Eczema/Craquele
Where does this primarily develop although can be anywhere
What does this look like on PE
How is Asteatotic Eczema/Craquele managed
AKA Winter itch- itch>rash in atopic Pts during winter months/after long hot showers
Anterolateral legs
Cracked porcelain- accentuated dry, scaly skin lines
Group 3-4 steroids then emollient
Emollient after bath
Dec shower frequency/temp
OIC= wet compress w/ ABX
Who/How does Nummular Eczema present
What does this Latin term indicate for it’s appearance on PE
Where is Nummular Eczema likely to develop on the body
How is Nummular Eczema managed
> 50y/o w/ reoccurring spot each year as intense itching leading to lichenification
Coin shaped pruritic plaques w/ sparse/thin flakes
Dorsal hands
Upper extremities
Lower legs
Humidifiers
Antipruritics PRN
Group 1-3 steroids x 4-6wks
Emolients
Lichen Simplex Chronicus (LSC) is AKA and d/t ?
LSC can be precipitated by ? Dxs?
How does LSC appear on PE and what are the nodules called
How is LCS managed
Neurodermatitis- scratching causes eczematous eruption
Contact dermatitis Atopic dermatitis Nummular eczema Seborrheic dermatitis Nerve entrapment
Red papules w/ thick plaques that accentuate skin lines
Nodules= Prurigo nodularis
Biofeedback/behavior modification
Unconscious scratching- 1st gen antihistamine
Group 1 steroid, wean w/ improvement
Nodules= Intralesional Kenalog
Stasis Dermatitis is an inflammatory result d/t ? physiological process
How does Stasis Dermatitis appear on PE
How is this condition Tx
Decreased circulation distends vessels
Dec membrane permeability= fluid/proteins into tissue
Extravasation- stasis purpura/hemosiderin deposits
Hyperpigmentation Itch Scaling
Prolonged= Ulcers
Topical steroids Emollients Elevation Compression
Define Atopic Dermatitis
What will almost always be in their Med/FamHx
When do these Pts tend to experience flare ups
Chronic pruritic eczematous Dz that almost always begins in childhood but improves w/ age
Atopy Allergies Asthma Sinusitis Hayfever
Cold/Hot weather Humidity Illness/Irritants Pollen Stress
Atopic Dermatitis is AKA ?
What is the morphology of this condition
What secondary issues can develop
How does the distribution of Atopic Dermatitis change w/ age
Itch that rashes: Dry= Crack= Itch= Rash
Papules/plaques
Lichenification
Dermographism
Autoinnoculated Staph infections
0-2: red scale on cheeks
2-12: flexural area, face, scalp
>12: bilateral flexors; spares the face, except eyelids
How is Atopic Dermatitis Tx in adults, kids, steroid failure and recalcitrant/topical failures?
What two meds can be used to break the scratch cycles
What medication is used second line for Atopic Dermatitis Tx if Pt is intolerant/resistant to other therapies but can’t be used in ? two populations
Adult inflammation: Triamcinolone Fluocinonide
Children, inflammation: Desonide Hydrocortisone
Steroid failure= Crisaborole BID
Mod-Sev/Recalcitrant/topical failure= Dupiliumab (IL-4 inhibitor)
Hydroxyzine, Diphenhydramine
Topical Calcineurin Inhibitors: Pime/Ta-crolimus
ImmComp; <2y/o
What is the name of the Atopic Dermatitis variant that presents during childhood
How is this variant Tx
Keratosis Pilaris- ASx spiny papules on extensor surfaces of arms/legs
Lotion w/ urea or lactic acid
Short course w/ mild steroid
Define Contact Dermatitis
What are the two types of Contact Dermatitis
How is the Dx made/confirmed
Eczematous dermatitis from exposures
Irritant (Occupation/Diaper): corneum barrier damaged; non-immunologic
Allergic: Ag absorbed, subsequent eruption
Patch testing
How do the 3 different phases of Irritant Dermatitis present
What part of the body is MC affected by this form oc contact dermatitis
How is this condition managed
Acute: Vesicle Exudate
Subacute: Cracked Inflamed Fissured
Chronic: Lichenification w/ less erythema
Hands, but can be anywhere
Avoidance
Cool compress
Emollient= protective barrier
Steroid, topical
? is the #1 and #2 MC cause of Allergic Contact Dermatitis and how does this eruption appear on PE
How is Dx of Allergic Contact Dermatitis made/confirmed
How is Allergic Contact Dermatitis managed
#1: Nickel #2: Poison ivy (Uroshiol) Pruritic Erythematous Crusty Swollen
Patch testing
Mild-Mod: topical steroid x 2wks
Sev: PO steroid x 2wks w/ taper
Antihistamine
Cool, wet compress
Define Urticaria
What causes Urticaria at the pathophysiological level and causes skin to take on ? appearance
Define Physical urticaria and what are the 6 types
Recurrent wheals (pruritic swelling of dermis that fade <24hrs)
Mast cell degranulation, histamine mediated response
Orange peel- dermis edema causes follicular accentuation
Dermographism Pressure Aquagenic Cholinergic Temp Solar
Timelines for acute/chronic urticaria
Which one can lead to anaphylaxis
What labs may be ordered during Dx phase prior to being referred to ?
Acute: 6wks or less w/ acutely reproducible effects
Chronic: >6wks, smaller and less severe, Dx of exclusion
Acute; Tx: IV/IM Benadryl, CCS, Epi
CBC LFT UA ESR
Allergy
How is Acute Urticaria Tx
How is Chronic Urticaria Tx
How is Physical Urticaria Tx
H1 antihistamine
Avoidance
Prep for anaphylaxis: Benadryl Epi CCS
2nd Gen antihistamine
H2 blocker
PO steroid
Elimination diet
Pre-Tx w/ H1 blocker
Angioedema MC affects ? areas of the body
How is this condition Tx
STOPPED
Lips Eye Tongue Trunk Genitals Hands
IM/PO Antihistamine
PO steroid, if ossible
Slide 14, Deck 5
? PE finding is indicator of Measles
How does the Measles rash appear
How does the Measles rash spread
How is Measles Tx/Protected
Koplik spots: white spots on buccal mucosa
Blanching maculopapular, erythematous rash
Face, centrifugally: head to feet
As it clears, leaves brown discoloration/scale
Fluids Antipyretic Respiratory isolation w/ humidifier
Notify health department
How does HFM Dz present
How is HFM Dz Tx
First: 2-10 painful oral papules to vesicles
Typically: dorsal finger/toes
Support
Anti-histamine/pyretic
Diet adjustment if painful PO lesions
? Dz is AKA 5th Dz
How does this rash appear
When is Erythema Infectiosum contagious
How is it Tx
Erythema Infectiosum- Slapped Cheek
Macular erythematous and lacy, worsened by exercise
Prodrome, not during rash
Support
Kawasaki’s Dz is AKA ?
How does it tend to present to clinic and what are two key identifiers?
What are the 3 phases of this Dz
Mucocutaneous Lymph Node Syndrome
7wks-12y/o w/ fever 101-104 and cervical adenopathy
Strawberry tongue
Tender edema to palms/soles
Acute: 7-14 days; Strawberry Edema Rash Fever
Subacute: No fever-25days; Thrombocytosis Arthralgia Desquamation
Convalescent: no clinical signs - norm ESR (6-8wks total)
? is the MC adverse effect of drugs
What are the four types of reactions
How does the MC type of reaction present
What are possible culprits for this occurence
Cutaneous eruption
Fixed eruption
Urticarial
Maculopapular
Exanthematous- MC
Maculoapular/Morbilliform- Mucus Palm Soles
Spares face
TMP/SMX Acetaminophen Barbituates Antimalarials NSAIDs
How does a Fixed Drug Eruption present
Since these tend to occur at the same time, every time, where can they develop
How are Cutaneous Drug Reactions Tx
What are the two types of Cutaneous Drug reactions that tend to have more serious complications
Single/few red plaques that blister soon after first exposure to medication
MC- glans penis
Lips Hands Face Feet- involves face
Steroids, PO/Topical Group 3-5
Antihistamines
D/c medication
Urticarial, Exanthematous
Define Erythema Multiforme
What are the two types
What are the two etiologies
Immune mediated condition causing target/iris lesions
Major: major mucosal involvement
Minor: mild/no mucosal involvement
HSV- MC
Mycoplasma pneumonia
Where does Erythema Multiforme affect the body
What can be expected from this condition’s duration
How is this Tx
Palm Extensor surfaces Dorsal hands Soles
70%- mucosal involvement, eye= stat referral
Develop x 3-5d, Last x 14d
Resolves w/ hyperpigmentation of skin
V/A-cyclovir Steroids, topical Orajel Antihistamine Prednisone if widespread
Define SJS
What c/c may precede this condition’s mucocutaneous Sxs
Commonly, these SJS/TEN PTs are on ? meds?
Where/How does SJS cutaneous Sxs present
Vesiculobullous dz of Genital Eye Mouth Skin
URI w/ fever 102* or >
Stinging eyes, painful swallowing
Bullous lesions 1-14d after prodrome on palm/soles
Seizure ABX Gout:
Lamotrigine Mycoplasma -oxicams Allopurinol
TMP/SMX
Flat target/purpuric macules- FIRST on trunk then neck, face and upper extremities
TEN is initially seen mimicking ? but is d/t ?
What is the MC cause of TEN and why does this condition have a high mortality rate
How does this present/develop
SJS mucous membrane Dz;
Epidermis toxicity, causes full thickness necrosis
MC cause: medication toxicity (same as SJS)
Mortality d/t sepsis
Conjunctivitis
Ulcerative vaginitis
Painful red, sunburned skin
Stomatitis
What PE sign is seen in TEN to aid w/ Dx
How is the necrotic epidermis described in this condition
? part of the body is spared and ? part is constantly involved
Nikolsky: slight pressure peels epidermis from dermis
Wet cigarette paper that shows raw, scalded looking dermis
Spares: Scalp, GI tract
Constant: Ocular
How is TEN Tx
What is not used
Traditionally, SJS/TEN were considered more severe forms of ? and graded/classified depending on ? criteria
Plasma exchange IVIG Cyclosporine A Cyclophosphamide
CCS
Erythema Multiforme:
SJS: mucosal erosion, <10% skin detached
Overlap: 10-30% detached
TEN: >30% detached
Erythema Nodosum is usually limited to ? parts of the body
? type of reaction is this one
How is this condition’s presentation different than the other 3 hypersensitivity reactions
Extensor aspects of extremities
Hypersensitivity
More common in females
Erythematous eruptions on extensor surfaces
Sarcoidosis association
What is the presentation for Erythema Nodosum
How are the characteristic lesions described and located
How is this Tx
Low fever Arthralgia Malaise Arthritis
Red node swelling over shins
Week 1: tense, hard, painful
Week 2: fluctuant
Self limited, NSAIDs
Define Pyoderma Gangrenosum
This commonly occurs in ? population
Where do lesions begin
Non-infectious neutrophilic ulcerating skin Dz
IBDz
Tender, red lesion w/ pustule/vesicle
Necrotizing inflammation moves peripherally, leaves necrotic ulcer w/ purulent base, lasts months-years
Acne Vulgaris is a multifactorial Dz involving ? unit
What are the 3 components of this pathogenesis
Why is puberty such a triggering time frame for Acne Vulgaris?
Pilosebaceous
Secretions Obstruction Bacterial colonization by P. Acnes: breaks down sebum into free fatty acids, causes irritation/inflammation
T converted to Dihydrotestosterone= inc sebum= acne
How is Acne Classified
What is the rule about these two classifications
Non-Inflammatory: Open/Closed comedome
Inflammatory: Papule Pustule Nodule/Cyst
Inflammatory can have comedones
Non-inflammatory will not have inflammatory lesions
Criteria for Mild Non-Inflammatory Acne and how is it Tx
Criteria for Mild Inflammatory Acne and how is it Tx
Criteria for Moderate Inflammatory Acne and how is it Tx
Criteria for Severe Inflammatory Acne and how is it Tx
+Comedone/Papule/Pustule, - nodules
Retinoid (Tretinoin/Adapalene)
F/u 4-8wks
BPeroxide and/or Topical ABX (Benzaclin- combo)
+Papule/Pustule, - nodule
Retinoid and/or BPeroxide or Topical ABX
+ pustules at f/u= PO Doxy/Mino/Tetra-cycline x 3mon
+ Papule/Pustule and Nodule
Topical Retinoid and BPeroxide and PO D/M/T-cycline
Nodules= Triamcinolone injection 2.5-5mg
++Papule/Pustule and Nodule
Minimal scarring= Sulfacetamide or Topical ABX w/ BPeroxide
Scars/Long TxHx/Depressed/RxFailure= Accutane
What is the next step if Pt fails Mild Inflammatory Acne Tx
What is the next step if Pt fails Moderate Inflammatory Acne retinoid Tx
What is the next step if they fail the above step
Female/RxFailure/Not Accutane candidate= OCP/Spironolactone
Accutane
Relapse after 2nd course= OCP/Spironolactone
What are the alternative/2nd and 3rd line Tx options for Acne Vulgaris Txs
Severe Nodulocystic Acne usually presents in ? populations
How is this form Tx
Tazarotene (retinoid) Azelac acid (topical ABX)
Male w/ + FamHx
Isotretinoin- impacts/alters P Acnes, Inflammation, Comedogenesis and Sebum produciton
What are the two approved indications for Isotretinoin useage
How are Pts screened for eligibility for use and pledge
What FamHx needs to be asked for d/t loose association w/ this medication use and what odd PT education piece is needed
Nodular/Recalcitrant acne
6mon follow time
D/c Tetracyclines/Topical retinoids/Vitamins, esp Vit A
CBC HCG UA LFT Lipids before Rx, repeat each f/u
Female- hCG Qmon during, 1mon after w/ 2 BCs
IBDz
Can’t donate blood during Tx
What are the indication to d/c Isotretinoin usage
How does Adult Female Acne present
How is Adult Female Acne Tx primarily (w/ MOAs), second and last line
Pregnancy Mood swings (SI/HI) S/Sx ICH: HA w/ vision change, unrelieved w/ OTC meds
Tender comedones on jaw/chin, worse during menses
Primary:
OCP- dec excess ovarian androgen suppression
Spironolactone- androgen receptor blockade
2nd: Tretinoin .025% cream
Last: Erythromycin 250mg
Who has Perioral Dermatitis and what PE finding is highly characteristic
What self-aid Hx is usually present in these PTs and w/ ? result
How is this condition managed systemically and locally
MC young females w/ pustules adjacent to nasolabial folds but clear border around vermillion border
Tried Bperoxide/Topical steroids w/ worsening Sxs
Systemic: Doxy and short use of HC cream
Local: Topical Erythromycin/Metronidazole
What is the suspected etiology behind Acne Rosacea
What is the morphology of this condition on PE
What will usually be in the Pts Hx
Since this can look similar to acne, what is missing on PE to differentiate the two Dxs
How is this condition Tx
Demodex Folliculorum
Rhinophyma
Swollen forehead/cheeks
Telangectasia
Long history of facial flushing leading to telangiectasia
Absence of comedones
Sunscreen/Avoidance Metronidazole, topical (first line) Azelaic acid Tetracylcine- severe/resistant Isotretinoin- refractory
Define Pomade Acne/Cosmetica
This usually involves forehead, temples and sides of the face, what areas can be spared?
How is this condition managed
Non-inflamed comedones in areas of product application
Sebaceous areas
Benzoyl Peroxide 10%
ABX for inflamed lesions
Tretinoin at bedtime
Stop all product use x 1mon
What 3 locations are MC affected by steroid acne
What is unique about this conditions morphology
How is Steroid Acne Tx
Chest Neck Back
Uniform size w/ symmetric distribution <4wks after PO CCS usage
No scarring, not c/i for further usage
D/c PO CCS
Benzoyl Peroxide and/or, Sulfacetamide lotion
Define Milia
Where do these MC appear
How are these managed
Epidermal cysts w/out openings d/t sun damage/physical trauma
Face, around eyelids
Few: Incision and excise, cannot express
Multiple: tretinoin until resolution
Define Miliaria
This can develop anywhere but especially ?
What structure is obstructed and causes the sweat retention etiology of this condition
How is it managed
Prickly eat rash; scattered skin-colored vesicles
Red= miliaria rubra
Forehead Trunk Cheeks
Eccrine gland occlusion
Anti-histamine, Cool compress
Define Hidradenitis Suppurativa
What is the etiology behind this condition
Where does this tend to occur
How is this condition staged for Tx
Painful, scarring of skin/SQ tissue ALWAYS presenting after puberty d/t invovlement of apocrine glands and folliculopilosebaceuous units
FamHx of scarring acne/hyperkeratosis over apocrine glands w/ secondary bacterial infections
Axilla Groin Infa-mammary
Hurley:
What morphology can Hidradenitis Suppurativa take on
What is a major trigger for this condition that is a part of Tx
What is the mainstay and other steps of Tx mild cases
How are extensive cases Tx
Double Comedone- black head w/ two or more communicating holes, healing makes band of scar tissue
D/c smoking
Tetracycline (DMET)= mainstay (Rosh says Topical Clinda) Hot compress InD- large cysts Steroid injections- smaller cysts
Surgical excision/grafts
Isotretinoin x 20wks
Define Staph Folliculitis
What is an uncommon Sx seen w/ this condition
This can develop as a complication of ? Tx
Painful pustules anywhere hair follicles are present w/ Staph A/E infection
Low fever
Occlusive topical steroids
What does it suggest if Pt has persistent/recurrent Staph Folliculitis
How is this Tx depending on the severity of outbreak?
How is this Tx if condition is persistent/recurrent
Nasal carrier
Isolated: topical Mupirocin/Clindamycin
Extensive: PO Dicloxacillin/Cephalexin
Hibiclens: hands, affected area
Mupirocin- nares
Clindamycin
What type of issue leads to PFB developing
How is PFB Tx
If on profile, Pts need to keep hairs how long?
Define Acne Keloidalis Nuchae
Foreign body reaction to hair= inflammation reaction from keratin and follicle distortion
BPeroxide wash Glycolic/Aveeno shaving cream Group 6-7 steroid on beard area after shaving Group 2-3- steroid larger lesions No resolution: add topical retinoid
<1/4”
Chronic scarring folliculitis w/out known etiology but coexists w/ PFB
If Acne Keloidalis Nuchae presents as pustular/exudative, how is it Tx?
What is the 3 step plan for controlling this condition?
Culture, Tetracycline x 3-6mon
Fluocinonide x3-6mon Tretinoin x12mon Clindamycin x12mon PO steroids Intrelesional injeciton Laser therapy Excisional surgery
Define EIC
These are more common in ? populations
How are these managed
Upper follicle occluded and dysfunctional, fills w/ sebum and swells
Oily sebaceous skin
FamHx cysts
Prone to acne
ASx/non-cosmetic: none
Non-inflammed: excision
Inflamed: Triamcinolone injection then excision
Ruptured: InD then excise
Pilar Cysts are AKA ?
How are these different than EICs
Nearly all will develop where and are Tx w/ ?
Wen
SubQ cyst w/ homogenous material that can calcify
Scalp, excision
What are the 5 topics of Papulosquamous D/os
What is the definition of the first type
What are the clinical presentations of the first types
Psoriasis Seborrheic Pityriasis Lichen Planus/Sclerosis
Immune mediated skin inflammation causing hyperkeratosis (7x faster; 4 vs 30 days)
Chronic Guttate Pustular Inverse
What do Chronic Psoriasis plaques look like
What ‘sign’ is seen if these plaques are picked off
Where is this disease distributed through the body
Flat, red papules w/ silvery scale
Auspitz- pin-point bleeding
Symmetric and Bilaterally:
Knee/Elbow extensor surfaces
Oil spot nails
What 3 medications can make Chronic Psoriasis worse
Sickness d/t ? type of microbe can cause this to worsen
How is Mild-Mod Psoriasis w/ <5% BSA Tx
Why is an analog used during Tx
BBs Lithium Systemic steroids
Strep
Salicylic acid then; Analog Vit D3 Clobetasol/Fluocinonide to Triamcinolone w/ holiday Calcipotriene- Vit D+Steroid combo UVB light therapy Tazarotene- topical retinoid (gel/cream)
Inhibit proliferation/neutrophils
Induces normal differentiation
How are Chronic Psoriasis- scalp lesions Tx
? Tx is best for moderate plaque psoriasis
What meds are used for facial/intertriginous psoriasis
What is the risk of using Tazarotene topical?
When is tar therapy most effective?
What therapy is ideal for chronic scalp/body plaques that are few/small in number
Traimcinolone spray/Fluocinolone solution
Diffuse/thick scale= Calcipotriene (Taclonex lotion)
Calcipotirol
Ta/Pimecrolimus w/ occlusion- doesn’t cause atrophy
Preg category x- excreted in milk
Combo w/ UVB therapy
Intralesion steroids
How is Chronic Psoriasis w/ >5% BSA Tx
Which ones are a-TNF, IL-17, IL-23 and p20 specific
Which ones are human Ab, fusion, human-ized Ab and chimeric Abs?
Which one is the only one w/out FDA and EMA approval
Biologics: Methotrexate Cyclosporine Aci/Iso-tretin UVA
a-TNF: Etanercept I/A-umab
17: SIB-umab
23: G-umab
p40: U-umab
Human: BAGUS-umab
Fusion: Etanercept
-ized: Ixek-umab
Chimeric: Inflix
Guse-umab
Define Guttate Psoriasis
What prodrome can precede ? presentation
What can cause Pts w/ Chronic Psoriasis to have a Guttate flare
What is first line Tx and later Txs?
Pts <20y/o, possible first indication of psoriasis
Strep pharyngitis/Viral URI- scaling pustules on trunk/extremities, spares palm/sole
Strep/Viral infection
First: UVB x 6-8ks
Analog Vit D Topical steroids Emollients
Where/how does Pustular Psoriasis present
What does this distribution develop as
How is it managed
What Tx needs to be avoided
Deep, creamy pustules on palm/sole that harden, fall off
Erythema forms on flexur areas, migrates to palm/sole
Pustules behind erythema
Cyclosporine Clobetasol Methotrexate Acitretin PUVA
PO steroids (induces severe Sxs) Smoking
What is the generalized variant of Pustular Psoriasis called
How do Pts present w/ this rare variant
Many Pts have ? Hx
von Zumbusch
Painful pustules Leukocytosis Febrile Toxic
Smoking
Define Psoriasis Inversus
What type of nail abnormality to these Pts have
Define Seborrheic Dermatitis
Flexur/Intertriginous scale that is macerated
Onycholysis
Subungual debris
Oil spots- localized separation of nail plate
Chronic inflammatory skin dz localized to areas w/ high sebum production
When does Seborrheic Dermatitis tend to peak in life
When do these Pts tend to have flares
What Pt populations tend to have more severe cases
This is one of the MC cutaneous manifestations of ? Dx
Teens Infancy Maternity (high hormonal periods)
Dryness Stress Hygiene changes
Elderly w/ neuro problems
AIDS
What is the etiology behind why Seborrheic Dermatitis exists
What morphology does this take on for PE
If this condition is long standing/chronic, what other issue is probably present
Over produced sebum
Over grown yeast (Malassezia furfur)
Greasy white/yellow flakes w/ pruritic/inflamed base
Staph infxn
How does the distribution of Seborrheic Dermatitis differ in infants and adolescent/adults?
What areas are less common to develop this condition
How is this Tx w/ shampoo, topical antigunal, topical steroid, secondary infections or mod/sev cases?
Infant- scalp vertex; Cradle Cap Adolescent/Adult- Posterior auricular fold External ear canal Nasolabial fold Eyebrow/eyelash base Scalp and margins
Presternal Umbilicus Groin Axilla
Shampoo/Topical: Ketoconazole
Steroid: Hczn/desonide (face) Fluocinolone (diffuse scalp)
Secondary infection: Diclox/Cephalexin
Mod-sev: PO Itraconazole
Pityriasis Rosea is d/t ? etiology and more common during ? times and in ? populations
How does this condition foreshadow and present
Where does the uncommon Reverse Pityriasis affect
HHV6/7 in 10-35y/o during colder months
Preceding URI, sudden Herald patch development- salmon pink in Christmas tree
Herald patch: trunk/prox extremities
Eruptive lesion: lower abdomen
Neck Face Palm/Sole
How is Pityriasis Rosea Tx
How are severe cases Tx
What odd DDx needs to be considered
Group 5 topical steroid
Antihistamine
Sunlight
Prednisone or,
UVB x 2wks or,
PO Acyclovir
Secondary syphillis
What type of reaction is Lichen Planus
This condition has an association w/ ? Dz
Define the Koebnerize phenomenon that occurs w/ this d/o
Inflamed skin/mucous membrane reaction
Hep C
Lesions form at site of skin trauma
What are the 5 P’s of Lichen Planus and what is the new, 6th P
What does the primary lesion look like
What type of striae may develop and how can they be seen
Pruritic Planar (flat topped) Polygonal Purple Papule/Plaque 6th: Persistent
Flat papule w/ polygonal border
Wickman’s- white, lacy pattern of criss-crossed lines; easier to see w/ immersion oil
How do Lichen Planus papules progress through different colors
What type of distribution does this condition present w/
Although the true etiology is unknown, what are the 3 proposed etiologies
Pink/white to purple w/ waxy appearance
Scalp: scarring hair loss Oral lesion- white, lacy Nail: splitting/dystrophy Genitals Acral: Hand Feet Ankle Wrist
Hep C Immune Drugs
How is a Lichen Planus Dx confirmed and why is this method needed
How is this managed if lesion is local, oral/resistant, generalized or itching
Biopsy to r/o SCC
Local: Group 1-2 w/ occlusion/injection q3wk
Oral: Clobetasol Fluocinonide Traimcinolone Azathioprine (resistant)
General: Prednisone
Itch: Hydroxyzine
Define Lichen Sclerosis
Where does this MC occur on the body
How do these manifestation appear early/later on
How is Lichen Sclerosis Tx
Inflammatory dz of superficial dermis/submucosa leading to ivory-white, scarring atrophy
Vulva Perianal Groin
Early: white-brown, horny follicular plugs
Later: porcelain/ivory w/ wrinkled atrophic surface
Topical Clobetasol: BID x 1mon, daily x 1mon
PUVA
What is the progressive morphology of Necrobiosis Lipoidica
What is the etiology of this condition
Nearly all lesions will occur ? on the body and if chronic, can develop into ?
How is it Tx
Purple ovals w/ red borders
Ulcerates, leaves woody induration
DM- diabetic microangiopathy
Anterior tib/fib;
SCC
Topical/Intralesion steroids: inflammation
PO steroids: stop Dz
Pentoxifylline
Who/where is Granuloma Annulare more likely to present
What do these lesions look like
The generalized form of this condition is associated w/ ? two systemic conditions
How are these Tx for cosmetic, disseminated, or generalized
Young/child w/ diabetic female on dorsal hand/feet (MC)
ASx flesh colored papule, Central involution, Inc diameter x months
DM or HIV
- Cosmetic: topical w/ occlusio/papular ring injection
- Disseminated- PUVA
- Generalized: HydroxyChlqn Isotretinoin Dapsone
What unique texture does Acanthosis Nigricans have
Where is this MC to be seen
Condition can be d/t malignancy, MC ? type
How can the lesions be Tx although they are ASx
Velvety, symmetrical thickening and hyperpigmentation of skin
Axilla
Gastric
Ammonium lactate- softens lesions
Tretinoin- thins skin
Define Xanthomas
What are the 5 types
Lipid deposits in skin/tendons from hyperlipidemia
Xanthelasma- MC type; yellow plaques near canthus; half have normal lipids
Eruptive- sudden yellow plaque on extensor surface/pressure point w/ red halo; sign of hypertriglyceride; rapidly resolve w/ drop of lipids
Tuberous- slow papule on extensor surfaces/palm; sign of hypertriglyceride or biliary cirrhosis; persist post-tx
Tendinous: MC on Achilles; sign of hyperlipidemia or biliary cirrhosis; persist post-tx
Tx: Trichloroacetic acid, risk altered pigment
Define Kaposi Sarcoma
What are the different types and characteristics of each
Vascular neoplasms usually on older male legs
Classic- slowly progressing on male hand/feet, move upward.
AIDS Pt- rapid development anywhere, MC head, face, neck
AIDS: slightly raised ovals w/ rapid progression to purple nodules
Dec in size w/ pressure, return w/ relief (differentiator from LP)
ImmSupp: d/t HHV-8
African Cutaneous/Lymphoadenopathic
What is the Classic Kaposi Sarcoma is the MC tumor in ? Pts
How is a Dx confirmed
How are these Tx
AIDS
Biopsy- proliferation of vessels w/ neoplastic endothelial cells
LN2
Vinblastine- intralesional chemo, better for lesion >1cm
Excision- single
Radiotherapy- larger masses
What are two types of finger nail issues seen in Hyperthyroidism
What type of lower extremity issue do they have
This can develop in Hypo/Hyper/Eu-thyroid but is mostly associated w/ ? thyroid condition
Thyroid Acropachy- digital clubbing w/ periosteal changes
Plummer’s nails- onycholysis w/ concave appearance
Dermopathy- AKA Pretibial Myxedema
Early: asymmetric, non-pitting
Late: symmetrical, orange peel appearance
Graves- hyperthyroidism
Vesicular and Bullous Dzs are autoimmune blistering Dzs w/ ? two characteristics
How are these Dzs characterized
These are classifed by ?
Impaired epidermis to basement adhesion
ABs against adhesion proteins
Substantial morbidity/mortality
Histology- level of skin separation
Define Pemphigus
What is the pathophysiological reason this occurs
When does this tend to occur and in ? population
Greek- blister, bubble;
Intraepidermal blister d/t loss of keratinocyte adhesion
IgG against Desmoglein 1 and 3: cell-cell adhesion in desmosomes
50-60y/o w/ Myasthenia Gravis w/ near universal involvement of oral mucosa
What do Pemphigus Vulgaris primary blisters look like
Why are these bad once they pop
How are they Dx
How is it Tx
Non-pruritic, thin walled w/ +Nikolsky
Rupture, painful erosion that ooze/bleed
Little/no healing occurs
Derm consult THEN
Skin biopsy for light microscopy
PRICC MAP:
Prednisone Rituximab IVIG Cyclosporine Cyclophosphamide Mycophenolate Azathioprine Plasmapheresis
? is the MC auto-immune sub-epidermal blistering Dz
Four differentiators about this MC
How are these Dx
How is this Tx
Bullous Pemphigoid
TENSE vesicles (PV- flaccid bullae)
Onsets >60y/o (pemphigus was 50-60y/o)
Pruritic bullous eruptions
Serous/hemorrhagic fluid
Derm consult THEN
Biopsy for light microscopy
Mild-Local: Group 1 topical steroid w/ PO CCS
Mod-Sev: same as PV (PRICC MAP)
Define Dermatitis Herpetiformis
What systemic dz is this associated w/
What population is this MC in
Intense burn/itch vesicular skin dz
Celiac dz
Northern European males
What is the classic distribution pattern for Dermatitis Herpetiformis
How is this Dx
How is this Tx short and long term
Symmetric, bilateral extensor surfaces
Scalp
Buttocks
Punch biopsy
Serological test- Celiac Dz
Short term: Dapsone
Long: gluten free diet
UV light is the MC cause of ?
What are the 3 types of UV light
Photobiologic skin reactions/Dzs
UVA: 320-400nm
Long waves, most constant year round
Penetrate deep, release free radical, alters DNA/Ca
Chronic exposure= CT degeneration/Photo-aging/allergy
UVB: 290-320nm
Greatest during summer, MOST harmful of waves
High amounts of energy to corneum/superficial layers
Pigmentation Inflammation Erythema Sun burn/tan
UVC: 100-290nm
Shortest wave, absorbed by the ozone layer
Transmitted only by artificial sources: germicidal lamp
What are the 6 Fitzpatrick phenotypes
What is the inverse relationship w/ these 6 classes
AES MDN
1: Always burns, never tans; blue eyes, red hair
2: Easily burns, barely tans; blond hair
3: Some burn, gradually tans; Mediterranean/Hispanic
4: Minimal burn, always tans well; darker hispanic/asians
5: Deep tan, rarely burns; Mid-east, Asian, some blacks
6: Never burns d/t deep pigmentation; blacks
Higher class= dec Ca risk
What environmental factors can affect amount of UV light exposure
Define SPF
Ozone: absorbs UVC
Clouds: 90% of UV light penetrates through
Sun elevation: peaks at 10am-3pm
Snow/Ice: reflects UVB
Sun Protection Factor: ratio of least amount of UVB required for minimal erythemal reaction through sunscreen compared to amount needed for same reaction w/out sunscreen
SPF 30- 30x longer exposure before burn
What are the 5 ways to optimize protection from UV damage
What are the body’s two natural sun protectors
What is the best protection method
Wear loos, dry clothes w/ wide hat Reapply q2hrs/after water exposure Avoid peak sun time 10A-3P Prior to outdoors, apply 15-30m SPF 15-30 daily
Statum corneum
Melanin
Clothing
What are the 3 MOAs of sunscreen
Define Photoaging
What four types of damage can the sun induce
Physical: titanium dioxide/zinc oxide- scatter/reflect light
Chemical: absorbs radiation
Water: proof x 80min/resistant x 40min
Skin changes superimposed on intrinsic aging from chronic exposures
Pigment Papular Texture Vascular
What are the 3 types of texture changes exposure can cause
What are the 4 types of vascular changes exposure can cause
What are the 3 types of pigmentation changes exposure can cause
What are the 4 types of papular changes exposure can cause
Atrophy- think skin, bruises easily
Rhomboidalis nuchae- deep wrinkles on neck that don’t disappear w/ stretching
Elastosis- thick skin w/ yellow hue
Venous lakes
Erythema/Ecchymosis
Stellate pseudoscars
Telangiectasis
Lentigo- large brown macules
Poikiloderma of Civatte: brown reticulated pigment w/ Telangiectasis, Atrophy, and Prominent follicles
Ephelides- freckles
Favre Racouchot- comedone/EIC around eye
Elastosis- thickened yellow skin
Nevi
SK
What is key for treating photoaging
What topicals are used for Tx
Prevention
Retinoids: Tretinoin/Tazarotene w/ sunscreen
Txs: Fine wrinkles Roughness Pigment
Won’t Tx: Coarse wrinkles, Telangiectasias
Define Polymorphous Light Eruption
What is the pathogenesis for this condition
When does this tend to present and w/ ? relationship to geography
What does the morphology look like
MC light induced skin Dz from UVB>UVA
Delayed hypersensitivity to endogenous photoinduced Ags
First 3 decades of life w/ inverse relation to latitude
Polymorphous and varies, but:
DPP- pin-head size groups in exposed areas
What phenomenon does Polymorphous Light Eruption cause
What are the 6 classical types of skin morphologies this condition causes
What is the clinical presentation of Polymorphous Light Eruptions
Hardening- Incremental doses of UV radiation based on tolerance/resolution
Papular- MC Plaque- 2nd MC Papulovesicular Eczematous Erythema multiforme Hemorrhagic
Malaise Chills HA Nausea x1-2hrs before rash, which heals w/out scars
How is PLME differentiated from Lupus
What type has mandatory Dx tests in order to r/o SLE
Delayed onset
Characteristic morphology
Histopahtlogical changes
Quick resolution
Plaque type: must get biopsy and Immunofluorescence