Dermatology Flashcards

(35 cards)

1
Q

What are the types of tumours of the epidermis?

A
  • Actinic keratosis
  • Bowen’s disease
  • SCC
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2
Q

Key features of Actinic Keratosis

A
  • Sun exposed areas- hands, nose etc
  • Yellow scaly plaque with irreg. edges
  • Tx- topical chemo, cyro, curettage, photodynamic therapy
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3
Q

Key features of Bowen’s Disease

A
  • Full thickeness dysplasia
  • Causes- sun, carcinogens, radio. ++immunosuppressed
  • Ix- biopsy
  • Tx- Cryo, curettage, excision, topical chemo, photodynamic therapy
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4
Q

Key features of SCC

A
  • Cause- sun, radio, carcinogens, mercury, progression from prev ulcer
  • Scaly/cruty raised area of skin with red inflamed base
  • Common in sun exposed areas
  • Ix- biopsy
  • Excition +/- radio
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5
Q

Types of basal cell skin tumours and Key features of BCC

A
  • Seborrheoic keratosis= wart. brown. middle aged.
  • Basal cell carincoma:
    • Cause= cumulative sun exposure
    • Pearly, rolled edges, telangectasia. Can form ulcer.
    • Invade local structure. don’t met.
    • Tx- excision, radio, curettage, cryo
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6
Q

Types of melanocytic lesions and key features of melanoma

A
  • Ephelis- freckle
  • Melanocytic naevus= benign pigmented macule
  • Lentigo= liver spot. Flat pigmented area.
  • Malignant melanoma:
    • Cause= BURN (UV B). trunk/ legs. pale people.
    • Presentation- asymmetrical, variable pigmentation, irregular edge, bleeding, itching, at least 6mm diameter
    • Met early and unpredictably
    • Ix= biopsy –> Breslow thickness
    • Tx= excision, chemo, radio
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7
Q

2 week wait referral criteria for melanoma

A
  • Dermatoscopy suggesting melanoma
  • OR 3 points from:
    • Major (2 points each): Change in size, irregular colour, irregular size
    • Minor (1 point each): >6mm, inflammation, oozing, change in sensation
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8
Q

What is cellulitis, what are common organisms and RF?

A
  • = Acute infection of lower dermis and SC tissue
  • Organisms: Strep. pyogenes (2/3), Staph. Aureus
  • RF:
    • Immunocompromise- steroids, DM, HIV, chemo
    • Entry point- wound, skin fissures, ulcer
    • CKD
    • Chronic liver disease
    • Alcoholism
    • PMH cellulitis
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9
Q

Presentation of cellulitis

A
  • Presentation:
    • Local- redness, hot, swelling, erythema, blisterds, erosions, abscess, purpura, purulent
    • Unilateral
    • Streaking away from lesion
    • Systemic- tachycardia, tachypnoea, malaise, fevers/chills, rigors, sepsis
    • Entry site? Wound, cannula, ulcer, bite
    • Lymphadenopathy
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10
Q

Complications of cellulitis

A
  • Necrotising fasciitis
  • Gas gangrene
  • Sepsis
  • Infections to other organs eg endocarditis, osteomyelitis
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11
Q

Ix and Tx of cellulitis

A
  • Ix:
    • Bedside- swabs (inc MRSA), obs
    • Bloods- WCC, CRP, cultures
    • Imaging- USS ?DVT, X-ray ?osteomyelitis
  • Tx:
    • Cons- rest, elevate, mobilise, fluids, draw margins.
    • Medical:
      • Analgesia
      • Antipyretics
      • ABx- 1. Fluclox (erythromicin). 2.Clindamicin. Co-amox if facial/ systemic.
      • MRSA- doxycycline
    • Surgical- debridement
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12
Q

Key features of necrotising fasciitis

A
  • = Rapidly progressive infection of deep fascia –> necrosis of SC tissue.
  • Presentation:
    • ++pain out of proportion
    • Rapidly spreading erythema, blistering, oedema
    • Systemic Sx- sepsis, fever, sweating, N+V, anorexia, diarrhoea
  • Ix- obs, swabs, bloods, x-ray
  • Tx:
    • ABCDE. Senior help ASAP!
    • ABx- micro. IV BenPen, gentamicin, clindamicin, metronidazole
    • Surgical debridement ASAP!
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13
Q

Presentation of eczema

A
  • Dry red and scaly patches
  • Itchy
  • Poorly demarcated rash. Acute= oozing papules + vesicles. Subacute= red + scaly.
  • Chronic –> lichenification. Skin thickening + exaggeration of skin markings.
  • Atopy= Eczema, hayfever, asthma. PMH/ FHx?
  • Triggers- fabrics, inhaled allergens, stress, heat, hormones, skin infections, dietary etc
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14
Q

Ix and Tx of eczema

A
  • Ix- usually none. IgE, RAST (specific Ab), patch testing
  • Tx:
    • Cons- avoid triggers and scratching. Soap substitutes eg dermol. Emollients- epaderm, diprobase
    • Medical= topical steroids. 1% hydrocortisone –> eumovate –> betnovate –> dermovate
    • 2nd line therapies- topical tacrolimus, phototherapy, ciclosporin, azathioprine
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15
Q

What are the eczema variants and their features?

A
  • Discoid- circular, oozing and crusting patches
  • Contact dermatitis to irritants eg soaps
  • Varicose eczema- varicose veins. Red/itchy. Borwn scars. Lipodermatosclerosis. –>?ulcer
  • Seborrhoeic dermatitis- red and scaly. Overgrowth of skin yeast. In eyebrows, scalp, cheeks, nasolabial folds. Tx= daktacort (miconazole + hydrocortisone)
  • Dyshydrotic eczema- blisters on soles of feet and hands. Related to stress and allergies
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16
Q

What is psoriasis? + RF/ aggravating factors

A
  • = AI disorer. Inflammation of dermis with epidermal hyperproliferation.
  • RF/ aggravating factors:
    • FHx
    • Stress
    • Smoking/ alcohol
    • Obesity
    • Infections (esp strep), skin injury
    • Hormonal
    • Meds- beta blockers, lithium, antimalarials
17
Q

Presentation of chronic plaque psoriasis

A
  • Itchy, dry patches +/- bleeding
  • Plaques- pink/red, scaly. Esp extensors (elbows, knees), lower back, scalp. Well demarcated and symmetrical.
  • Nail changes- pitting, onycholysis
  • 10-40% –> seronegative arthritis (mono/polyarthritis). Asymmetrical. DIPs.
18
Q

Variants of psoriasis and their presentation

A
  • Pustular- palms and soles
  • Guttate- Sudden. 2-3w post strep throat. Papules on trunk.
  • Flexural- older people. No scale. Groin, nasal cleft, submammary
19
Q

Tx of psoriasis

A
  • Cons- avoid triggers, soap substitutes eg aqueous cream. Emollients eg epaderm/dermol/diprobase.
  • Topical therapy- steroids, Vit D3 analogue (calciprotriol), tar, retinoids (eg tazarotene).
  • UVB phototherapy
  • Systemic:
    • Biological- anti-TNFalpha eg infliximab
    • Non-biological- methotrexate, ciclosporin
20
Q

What is Tinea and its types? + Tx

A
  • Tinea= superficial mycosis caused by dermatophytes (fungi)
  • Presentation= Round, scaly, itchy lesions with central clearing. Slightly raised. Well demarcated. Scaly edge.
  • Types:
    • Tinea corporis= symmetrical. spreading. on body.
    • Tinea faciei= face.
    • Tinea cruris= Groin. More red and plaque-like.
    • Tinea pedis= athlete’s foot. ++ itchy. Fissured and macerated skin.
  • Tx= topical antifingals eg clotrimazole. PO if widespread.
21
Q

What is scabies? Presentation, Ix and Tx

A
  • = Skin infection with saropptoes scabiei
  • Rash- ++ itchy, papular. Site- interdigital, ankles, wrist, axillae, umbilicus
  • Linear skin burrows= pathopneumonic.
  • Ix- skin scraping
  • Tx- wash clothes/ sheets. Scabicide to whole body eg malathion.
  • ++ Contagious
22
Q

What is candida albicans? Presentation + Tx

A
  • = Yeast infection.
  • Thrives in warm moist areas- nappies, body fold, interdigital space.
  • Rash- Erythematous, ragged, peeling edge +/- small pustules
  • Mouth + genital- white plaques/ discharge
  • Tx:
    • Cons- clean and dry skin
    • Topical antifugal- cream eg clotrimazole, drops eg nystatin, pessaries eg clotrimazole.
    • PO Fluconazole if resistant
23
Q

What are the key features of acne vulgaris?

A
  1. Keratinocyte proliferation
  2. ++ Sebum
  3. Bacteria colonisation
  4. Inflammatiion
  5. White and black heads
24
Q

Tx of acne vulgaris

A
  • Cons- screen for mental health
  • Med:
    1. Topical ABx + bezoyl peroxide
    2. PO ABx 4-6m + bezoyl peroxide. Eg doxycycline.
    3. ?OCP
    4. –> Specialist. Isotretanoin. SE= dryness, depression, teratogenic
25
What is acne rosacea and how does it present?
* = Chronic relapsing remitting disorder of BVs adn pilosebaceous units * Presentation: * More in fair skinned * Pre-rosacea- flushing in repsone to stress etc * Central rash- symmetrical, erythema, telangectasia, papules, pustules, inflamm nodules
26
Tx of acne rosacea
* Cons- soap substitutes. Sun cream. * Med: 1. Topical metronidazole 2. PO doxycycline 3. Isotretanoin
27
What is erythema multiforme? Presentation + Tx
* = Hypersensitivity. Mostly to HSV * Rash- Erythematous, round, well defined 'target lesions'. Extensor surfaces. Lesions at different stages (multiforme) * Major= severe mucosal involvement, systemic upset. * Tx= usually none. ?Steroids ?aciclovir
28
What is Steven-Johnson Syndrome- causes, presentation
* = Serious disease of skin and mucous membranes. Hypersensitivity reaction to drugs/ infection * Drugs- NSAIDs, penicillins, anti-epileptics, sulfonamides * Presentation- Starat drug --\> vague URTI Sx for 2-3w --\> painful erythematous macules --\> severe mucosal ulcerations
29
Erythroderma - What is it? Presentation, complications, Tx
* = Intense widespread reddening of skin due to inflammatory skin diseases. 'Red man syndrome' * Causes/ RF: Drug eruption, dermatitis, psoriasis, infection, systemic disease (HIV, GVHD, malignancy). * Presentation: * Often preceded by eruptions, plaques, dermatitis. * Generalised erythema (\>90% skin surface). Warm. * Oedema * Systemic- lymphadenopathy, hepatosplenomegaly * Complications- hypothermia, dehydration, electrolyte imbalance, HF, secondary skin inf, hypoalbuminaemia (--\> oedema) * Tx- Regulate body temp, fluid status and electrolytes. Wet wraps, emollients (thick white paraffin), topical steroids.
30
What are the types of malignant melanoma?
* Superficial spreading * Nodular * Lentigo maligna melanoma (face. prev. lentigo maligna) * Acral lentigenous melanoma (nails) * Amelanotic melanoma
31
Types of severe cutaneous drug reaction and presentation
* Widespread macular papular rash. * Features of severe: * Temp \>40 * Hypotension * Lymphadenopathy * SOB/ wheeze * Erythroderma * Swelling of face/ tongue * Pain/ burning * Erosions/ shearing * Blistering/ bullae * SJS= \<10% surface areas with blisters * TEN= \>30%. Toxic epidermal necrolysis.
32
Presentation of eczema herpeticum + Ix and Tx
* Sudden deterioration of stable eczema: * ++ pain * Unwell +/- fever * Small punched out ulcers (can merge) * Dissemination * Ix- viral swabs * Tx- PO aciclovir +/- flucloxicillin
33
What is staphylococcal scaled skin syndrome?
* Esp infants, elderly, immunocompromised. * Infection of Staph (may not be skin) --\> release epidermolytic toxins * Mucosal surface never involved, no necrosis * Look for local focus eg nasopharynx * Ix- blood culture and swabs * Tx= fluclox
34
Types of Bullous skin disorders + key features
* Bullous pemphigoid- Elderly w/ neuro disease. Itchy skin with large tense bullae. Risk of infection. Tx= steroids * Pemphigoid vulgaris- younger, more severe. Flaccid superficial blisters. Tx- systemic steroids/ immunosuppression * Dermatitis herpetiformis- Esp in coeliac. Sysmmetrical ++ itchy blisters. +/- GI Sx. Tx= gluten free
35
Categories of skin lesion morphology
* Flat: Macule \<0.5cm, patch \>0.5cm * Raised: Papule \<0.5cm, nodule \>0.5cm * Plaque= large, plateau, superficial * Fluid filled: vesicle= \<0.5cm, bulla= \>0.5cm, pustule= pus filled * Abscess= fluid filled lesion