Dermatology
Editor: Ashley Ciosek, MD
Reviewed by Eva Niklinska, MD
| Terminology | |
|---|---|
| Primary Lesions | |
| Term | Definition |
| Macule | Flat, \< 5mm |
| Patch | Flat, > 5mm |
| Papule | Raised, \< 5mm |
| Plaque | Raised, > 5mm |
| Vesicle | Fluid filled, \< 5mm |
| Bullae | Fluid filled, > 5mm |
| Pustule | Pus filled |
| Nodule | Firm, thicker, deeper, typically 1-2cm in diameter |
| Petechial | Non-blanching, \< 4mm |
| Purpura | Non-blanching, 4-10mm |
| Secondary Lesions | |
| Term | Definition |
| Excoriations | Excavations dug into skin secondary to scratching |
| Lichenification | Roughening of the skin with accentuation of skin markings |
| Scale | Flakes of stratum corneum |
| Crust | Rough surface, dried serum, blood, bacteria and cellular debris |
| Ulceration | Loss of both epidermis and dermis |
| Erosion | Loss of epidermis |
| Corticosteroid Potencies: | |||
|---|---|---|---|
| Low Potency | Medium Potency | High Potency | Very High Potency |
| Desonide 0.05% (cream, lotion, ointment) | Triamcinolone (Kenalog) 0.1% (ointment, cream) | Betamethasone dipropionate 0.05% (ointment, cream, lotion) | Clobetasol 0.05% (cream, ointment, lotion, gel, foam) |
| Triamcinolone (Kenalog) 0.025% (ointment, cream) | Hydrocortisone valerate 0.2% (ointment, cream) | Triamcinolone (Kenalog) 0.5% (ointment, cream) | |
| Hydrocortisone acetate (OTC) |
Corticosteroids: General Principles
- Main side effects ➔ skin atrophy
- Face and intertriginous areas ➔ low potency steroids ONLY
-
High potency steroids should be limited to 3 weeks of use
-
Optimal absorption if applied after bathing (hydration promotes steroid penetration)
- Ointments - most potent due to occlusive effect, good for thick, hyperkeratotic lesions and areas of smooth, NON-hairy skin. Avoid hairy and intertriginous areas (can cause skin maceration and folliculitis)
- Creams - more cosmetically appealing and well tolerated. Less potent than ointments
- Lotions - Useful in hairy and intertriginous areas. Less potent than creams
Common Rashes
Morbilliform Drug Rash:
- Description:
- - Erythematous macules ➔ confluent papules
- - Trunk ➔ extremities, symmetric
- - Most common precipitants \= antibiotics (beta-lactam antibiotics, sulfa drugs), allopurinol, AEDs, NSAIDs
- - Sx: Pruritus, low grade fever
- Management
- - Discontinue offending agent
- - Topical Corticosteroids, wet wraps
- - Antihistamines
- - If eosinophilia, kidney/liver dysfunction, mucous membrane lesions or painful/dusky lesions, consider alternative diagnoses (DRESS, AGEP, SJS/TEN)
Erythema Multiforme
- Description:
- - Abrupt onset of papular “target” lesions in symmetrical acrofacial sites, +/-mucosal involvement
- - Usually precipitated by HSV
- - Sx: Lesions can be painful, pruritic or swollen
- - Systemic symptoms likely attributed to inciting infection (HSV, CMV, EBV, flu, COVID, etc)
- Management:
- - Oral antihistamines and/or topical steroids for itch
- - Treat precipitating infections (HSV tx does not alter course of single episode, can help prevent future inf)
- - Stop offending medications
- - If recurrent, derm referral for prolonged antiviral course
Zoster
- Description:
- - Reactivation of VZV leading to blistering, painful rash in dermatomal distribution
- - Rash can last 3-4 weeks
- - Sx: Painful pustular lesions with systemic symptoms including fever, headache and lymphadenopathy
- Management:
- - Best treatment is prevention (shingles vaccine in adults >50)
- - Valacyclovir 1000 mg TID if symptoms started w/in 72 hours and patient has new lesions) for 7 days OR acyclovir 800 mg 5x daily for 7 days
- - Can be complicated by post-herpetic neuralgia, manage w/ early antiviral treatment, topical capsaicin, TCAs, gabapentin/pregabalin
Seborrheic Dermatitis
- Description:
- - Inflammatory response to Malassezia yeasts
- - Characterized by erythematous w/ yellowish and greasy scale of scalp, face, upper trunk, intertriginous areas
- - Can be associated with HIV, Parkinson's disease and use of neuroleptic medications ; consider rescreening everyone for HIV
- - Chronic, relapsing (mildest form \= dandruff)
- - Sx: Usually non-pruritic
- Management:
- - Mild symptoms + isolated to scalp (i.e. dandruff) ➔ antifungal shampoo (Rx: ketoconazole 2%, OTC: selenium sulfide 2.5%)
- - Moderate/severe symptoms w/ scale, inflammation and pruritus of the scalp➔ antifungal shampoo + 2 week high potency topical corticosteroid followed by 2x weekly use of high potency topical steroids
Tinea
- - Pedis - “athlete’s foot”
- - Corporis - body ringworm
- - Capitis - scalp ringworm
- - Cruris - “jock itch”
- - Onychomycosis - fungal nail infection
- Description:
- - Presentation depends on location
- - Pedis: itchy erosions/scales between toes, hyperkeratosis/scale covering soles/sides of feet, vesiculobullous blisters of inner aspect of foot
- - Corporis: solitary circular red patch with raised scaly leading edge, forms ring-shape with hypopigmentation
- - Capitis: partial hair loss, +/- erythema, +/- pustular lesions
- - Curis: erythematous bilateral but asymmetrical rash with raised border and central clearing
- - Onychomycosis
- - Perform KOH preparation if possible to confirm diagnosis
- - Sx: Can be itchy and erythematous or asymptomatic
- Management:
- Treat all sources of tinea to prevent re-infection.
- - Nystatin IS NOT effective treatment
- - Pedis/Corporis/Cruris: if localized infection ok for topical antifungals (clotrimazole 1% BID until clinical resolution 1-4 weeks)
- - Capitis: Oral griseofulvin (500-1000 mg daily for 4-6 weeks) or oral terbinafine (250 mg once daily for 4 to 6 weeks)
- - Onychomycosis: Oral terbinafine (250 mg once daily for 6 weeks (fingernail) or 12 weeks (toenail)), topical therapy (efinaconazole, amorolfine, ciclopirox)
Paronychia
- Description:
- - Inflammation of the skin around a finger or toenail
- - Can be associated with felon (painful abscess at the base of the toe/nail) or herpetic whitlow (viral cutaneous infection caused by HSV)
- - Usually due to staph/strep or pseudomonas
- - Sx: Pain at the site of the infection, can develop systemic infection leading to fever/chills/myalgias
- Management:
- - If no abscess formation, can manage with soaking affected digit in warm water and antiseptics (chlorhexidine soaks TID) with mupirocin applied after soaking
- - If abscess present ➔ I\&D + culture
- - Antibiotics indicated if symptoms not improving after I\&D or systemic symptoms (dicloxacillin 250-500 mg QID, cephalexin 500 mg QID) for 5 day duration
- - If risk factors for MRSA ➔ Bactrim 1-2 DS tablets BID
- - If oral flora present ➔ augmentin 875/125 mg BID
HSV
- Description:
- - Present as clusters of 2-3 mm umbilicated clear or hemorrhagic vesicles persisting for 5-10 days usually preceded by localized tingling/burning
- - Type 1 most commonly associated with oral lesions, Type 2 w/ genital lesions
- - Diagnose with viral culture of swab from vesicle or serologic testing (may be positive and not causing symptoms)
- - Sx: Lesions are painful, can be associated with mild malaise and fever
- Management:
- - No cure, following initial infection immunity develops but does not prevent against further attacks
- - Tx w/ topical therapy for mild infections
- - For initial infection: Valacyclovir 500 mg BID 3-5 d, acyclovir 200 mg 5x/d for 5 days
- - For recurrent infections: oral valacyclovir 500 mg BID for 3 days or 1 g daily for 5 days OR Acyclovir 800 mg BID for 5 days
- - For suppressive therapy: oral valacyclovir 500 mg or 1 g daily
Candida (Balanitis, Intertrigo)
- Description::
- - Balanitis: inflammatory versus infectious condition of the glans penis. Most commonly infectious cause (candida versus dermatophytosis)
- - Sx: penile soreness, dysuria, itchiness, bleeding and erythema of the glans
- - Candidal balanitis associated with white, curd-like exudate
- - Intertrigo: erythematous/macerated plaques with peripheral scaling, often associated with superficial satellite papules or pustules
- - Affects skin below breasts or under abdomen, armpits, groin and web spaces between fingers/toes
- Management:
- - Balanitis: attention to genital hygiene with retraction of foreskin and cleansing for prevention/therapy
- - Clotrimazole cream BID for 7-14 days
- - Intertrigo: Prevention with moisture-free skin, can use talcum powder to assist in intertriginous areas
- - Topical antifungal agents (clotrimazole 1% cream BID for 4 weeks, 1% ointment BID for 2 weeks)
- - Oral fluconazole or itraconazole for severe, generalized and/or refractory cases
Pityriasis versicolor
Pityriasis Rosacea
- Description:
- - Pityriasis versicolor: Superficial fungal skin infection caused by Malassezia
- - Hypo/hyperpigmented or erythematous macules/patches or thin plaques most common on upper trunk, upper extremities
- -Sx: usually asymptomatic
- - Pityriasis rosacea: Self-limiting rash (6-10 weeks) characterized by large circular/oval “herald patch” found on chest/abdomen or back followed by small scaly oval red patches on back and chest (sometimes described in Christmas tree pattern)
- - Sx: vary from mild to severe itching. ⅔ of patients have flu-like symptoms prior to rash onset
- Management:
- - Pityriasis versicolor: Topical antifungal treatment with ketoconazole 2% shampoo (Daily for 3 days), selenium sulfide 2.25% shampoo or terbinafine 1% cream
- - Pityriasis rosacea: Self-limiting disease therefore treatment is symptom management
- - Apply daily moisturizing creams, avoid drying soaps
- - Can trial medium potency topical steroids and oral antihistamines
Atopic dermatitis (eczema)
- Description:
- - Lesions are pruritic, erythematous, +/- weeping/exudative, +/- blistering. Can become lichenified and scaly with fissuring over time.
- - Most commonly occurs on neck, hands and flexural surfaces in adults
- - Associated with atopic triad (asthma, eczema, and allergies)
- Management:
- - Avoid triggers (fabrics, chemicals, humidity, and dryness, foods)
- - Daily skin hydration w/ emollients ointments > creams (take into consideration patient tolerability)
- - Topical corticosteroids: Mild disease - hydrocortisone 2.5% BID until 3-5 d after skin clearance. Moderate disease - triamcinolone 0.1% or 0.025% Clobetasol cream for up to two weeks followed by mild steroids
- - Skin and face folds treatment: Desonide 0.05% OR topical calcineurin inhibitors (tacrolimus 0.1% BID, discontinue when symptoms cleared)
Psoriasis
- Description:
- - Clearly defined red and scaly plaques, symmetrically distributed
- - Most common locations are scalp, elbows, knees
- - Sx: Pruritus is common but mostly mild, treating can lead to hyper/hypopigmented plaques that fade over time
- Management:
- - Limited disease ➔topical corticosteroids and emollients
- - Scalp/external ear canal: potent corticosteroids - clobetasol propionate 0.05% BID until lesions clear
- - Face/intertriginous: low-potency OTC hydrocortisone 1% or prescription-strength 2.5% BID until lesions clear
- - Thick plaques on extensor surfaces: clobetasol propionate 0.05% BID until lesions clear
- - Moderate to Severe ➔ Phototherapy + topical steroids/emollients, before systemic agents (e.g. MTX)
Acne:
- Description:
- - Open and closed comedones, noninflammatory versus inflamed papules/pustules
- - Severe cases involve nodules, pseudocysts with scarring
- Management:
- - sunscreen SPF >=30 daily with broad spectrum coverage
- -Mild acne: daily topical retinoid (tretinoin) + benzoyl peroxide (if papulopustular lesions present)
- - Moderate/severe: Isotretinoin (cumulative dose of 120-150 mg/kg)
- - If isotretinoin is contraindicated, consider oral doxy (100 mg daily for 3-4 m) OR OCP OR spironolactone (25 to 50 mg/day in 1 to 2 divided doses, titrate based on response/tolerability)
Allergic contact dermatitis
- Description:
- - Type of eczema caused by allergic reaction to allergen (type IV hypersensitivity), usually 48-72 hours after exposure
- - Symptoms include erythematous, indurated pruritic plaques, +/- edema, +/- blistering, +/- scale
- - Consider triggers such as nickel, fragrances/perfumes, work exposures, poison ivy
- Management:
- - Determine allergen, if not identified easily, can have comprehensive patch testing
- - Acute/localized rash on hands/feet or nonflexural areas ➔ high potency topical corticosteroids BID until resolution (up to 4 weeks) then taper over 2 weeks
- - Acute/localized rash on face/flexural areas ➔ medium/low potency topical steroids BID for 1-2 weeks then taper over 2 weeks OR topical tacrolimus 0.1% until resolution then taper
Stasis dermatitis
- Description:
- - Caused by venous hypertension resulting from dysfunction of venous valves, obstruction to venous flow
- - Sx: include edema, inflammatory skin changes, pruritus, tenderness, ulceration, varicosity and hyperpigmentation (hemosiderin deposition)
- Management:
- - Compression therapy with bandaging systems or stockings, elevation of legs, regular exercise other than standing
- - Emollient (petroleum jelly) application for dryness/pruritus
- - Acute disease w/ erythema, pruritus, vesiculation, and oozing ➔ consider high/mid-potency topical corticosteroids BID for 1-2 weeks
- - Referral to vascular if persistent symptoms
Rosacea
- Description:
- - Chronic inflammatory condition affecting central face, usually appears between 30-60 yo
- - Persistent facial redness, telangiectasia, thickening of skin and possible development of inflammatory papules/pustules.
- - Pathophysiology multifactorial, includes genetic susceptibility, immune dysregulation, neurocutaneous triggers (sunlight, temperature, exercise, spicy foods, alcohol, stress, tobacco)
- Management:
- - Learn/avoid triggers (alcohol, tobacco), use gentle skin care products, and sun protection
- - Consider pharmacological intervention with topical brimonidine, laser or intense pulsed light therapy
- - If complicated by papular/pustular disease, consider topical metronidazole 0.75% gel for mild disease, and oral tetracycline/doxycycline for moderate to severe disease
Inpatient dermatology
SJS/TEN
- Description:
- - sheet-like skin and mucosal loss
- - SJS \<10% BSA, Overlap 10-30%, TEN >30% BSA
- - incidence: 1-2 affected per million
- - slightly more common in females. 100X more common in HIV
- -most common culprits:
- -Sulfonamides: cotrimoxazole
- -Beta-lactam: penicillins, cephalosporins
- -Anti-convulsants: lamotrigine, carbamazepine, phenytoin, phenobarbitone
- -Allopurinol
- -Paracetamol/acetaminophen
- -Nevirapine (non-nucleoside reverse transcriptase inhibitor
- -Nonsteroidal anti-inflammatory drugs (NSAIDs) (oxicam type mainly).
- -usually preceded by flu-like illness: aches, pains, fever, sore throat, conjunctivitis
- -pt typically with marked pain and extremely anxious
- -mortality rate 10% SJS, 30% TEN; can be more accurately predicted with SCORTEN score
- Management:
- -cessation of causative / suspect drugs --consider burns unit admission for wound care management
- -pain management
- -early involvement derm and ophthalmology teams
- -system steroids of unclear efficacy given wound care & infection concerns
- -heated room 30-32degrees
- -consider alternative diagnoses (DRESS, AGEP)
Prickly heat rash
- Description:
- - Heat causes exocrine gland blockage, resulting in raised, itchy rash.
- -associated with former heating pad sites, abundance of blankets
- Management:
- -Take cool baths or showers; tap dry; use cold compresses
- -Wear loose cotton clothing.
- -Use lightweight bedding.
- -Drink plenty of fluid to avoid dehydration.
Leukocytoclastic vasculitis
- Description:
- -inflamed small blood vessels due to infiltration of neutrophils into blood vessel walls
- -rash caused by small areas hemorrhage, resulting in purple red lesions (palpable purpura)
- -punch biopsy to confirm diagnosis
- -frequently occurs in association w/ systemic dx: infection, SLE, RA, Sjogren, malignancy
- Management:
- -early involvement of dermatology: after confirmation via punch biopsy, treat most likely underlying source of disease --tx often involves systemic corticosteroids
DRESS - Drug Reaction with Eosinophilia and Systemic Symptoms
- Description:
- RegiSCAR inclusion criteria for potential cases require at least 3 of the following:
- 1. Hospitalization
- 2. Reaction suspected to be drug-related
- 3. Acute skin rash
- 4. Fever above 38C
- 5. Enlarged lymph nodes at two sites
- 6. Involvement of at least one internal organ
- 7. Blood count abnormalities such as low platelets, raised eosinophils, or abnormal lymphocyte count.--morbilliform drug reaction + erythroderma + facial swelling + mucosal involvement
- -causative agents: allopurinol (esp together with thiazide), sulfa drugs, carbamazepine, phenobarb, phenytoin, iodinated contrast
- -onset \~ 2 weeks of inciting drug
- Management:
- -withdraw all suspected meds --systemic corticosteroids with slow prolonged taper
- -supportive tx with unscented emollients, topical corticosteroids
Pyoderma gangrenosum
- Description:
- -rapidly enlarging, painful ulcer, autoinflammatory etiology
- -full thickness with purple/blue undermined borders
- -50% cases have an underlying disease pathology, ex: IBD (UC>Chron's), RA, leukemia, IgA gammopathy, GPA, Behcet
- Management:
- -mostly non-surgical, though skin grafting may be necessary after active phase
- -potent topical steroid, tacrolimus ointment, oral doxycycline
- -large ulcers may require: oral steroids, anti-TNF (anakinra, infliximab, etanercept) -avoidance of local trauma
Toxic shock syndrome
- Description:
- -pathophys: localized staph infection → bacterial exotoxins trigger massive cytokine release, producing rash (sunburn appearance), fever, hypotension
- -initial phase: diffuse macular rash, "sunburn appearance", fever, multiorgan abnormalities
- -secondary phase: 1-2 wks later: shedding skin in large sheets
- -prior toxic shock sis a risk factor for recurrence
- -majority of cases are surprisingly previously healthy adults aged 20-50
- -complications: ARDS, DIC
- Management:
- -peripheral blood cultures to isolate causative strain. Typically, will use penicillin (or Vanc allergy) + clindamycin
Cutaneous blastomycosis
- Description:
- -skin lesions starting as papules, or pustules. Over course of weeks, develop into ulcerated/crusty sores
- -heal to form raised wart-like scars
- -screen all for HIV
- -when the infection spreads and skin becomes involved, spontaneous resolution does not occur and treatment is necessary.
- Management:
- -treat underlying immunosuppressive condition, for example, HIV
- -ID consult warranted: skin involvement necessitates treatment bc spontaneous resolution does not occur: mild-moderate disease treat with itraconazole, severe disease treat with amphotericin B
RMSF (Rocky Mountain Spotted Fever)
- Description:
- -centripetal rash: begins on hands/wrists, ankles, spreads centrally towards trunk/abdomen. face typically rash-free in beginning of course. Starts as red macules, then becomes papular and petechial
- Management:
- --tx: doxycycline, other tetracyclines. Pregnant females require ID consult.
MIRM (Mycoplasma induced rash and mucositis)
- Description:
- -affects younger demographic than SJS/TEN
- -causative agent \= mycoplasma pneumoniae
- -predominant mucosal & occular features, with fewer cutaneous features than SJS/TEN
- MIRM criteria:
- \<10% BSA with detachment:
- > 2 mucosal sites involved
- Few cutaneous vesiculobullous lesions
- Atypical pneumonia present
- Labs: increase in M. Pneumoniae IgM antibodies, M. Pneumoniae in oropharyngeal or bullae cultures or PCR, and/or serial cold agglutinins
- Management:
- -early Optho and Derm involvement (esp since SJS/TEN should be ruled out):
- -typically, optho will recommend antibiotic drop QID, cyclosporine BID, steroid drops BID, and combo abx / steroid ointment to eyelid margins BID to QID