Lectrue ILO’s Flashcards

1
Q

Finger clubbing

A

Clubbing
• Loss of angle between the posterior nail fold and nail plate
• Loss of Schamroth’s window
• Always take note – can be a sign of serious disease
• Associated with lung malignancy, IBD, cirrhosis, cardiac problems, supparative lung problems, interstitial lung disease, Grave’s disease - lung disease which causes depleted blood oxygen levels

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2
Q

Nail pitting

A

Pitting
• Punctuate depressions of the nail plate
• Usually psoriasis (also eczema/alopecia)

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3
Q

Koilonychia

A

Koilonychia
• Spoon-shaped depression of the nail plate
• Iron deficiency anaemia

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4
Q

Onycholysis

A

• Loosening or separation of the nail plate from the nail bed
• Causes include repetitive trauma, nail infections, manicures, drugs, hereditary, psoriasis, myeloma, diabetes, thyroid disease, leprosy

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5
Q

General Terminology

Pruritis
Lesion
Rash
Naevus
Comedones

A

• Pruritis - Itching

• Lesion - An area of altered skin

• Rash - An eruption

• Naevus - Localised malformation (ie. moles)

• Comedones - Spots – open are blackheads/closed are whiteheads

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6
Q

Erythema

A

Redness (due to inflammation and vasodilation) that blanches with pressure

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7
Q

Purpura

A

• Purpura
• Red or purple discolouration (caused by bleeding into the skin) that does NOT blanch with pressure

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8
Q

Hypopigmentation

A

• Hypopigmentation
Areas of pale or paler skin

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9
Q

Dipigmentation

A

• Depigmentation
Areas of skin with no pigement, due to a lack of melanin

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10
Q

Hyperpigmentation

A

Hyperpigementation Areas of skin with darker colouration

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11
Q

Macule

A

Macule
Flat area of altered colour
Ie a freckle

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12
Q

Plaque

A

• Plaque
Scaling lesion, raised and palpable

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13
Q

Papule

A

• Papule
Solid raised lesion <0.5cm

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14
Q

Vesicle

A

• Vesicle
Fluid-filled raised lesion <0.5cm

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15
Q

Nodule

A

• Nodule
Solid raised lesion >0.5cm

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16
Q

Bulla

A

• Bulla
Fluid-filled raised lesion >0.5cm

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17
Q

Pustule

A

• Pustule
Pus-filled, <0.5cm

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18
Q

Boil or furnacle

A

• Boil or Furuncle
Staph infection of hair follicle

• Carbuncle
Several furuncles

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19
Q

Abscess

A

• Abcess
Localised collection of pus

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20
Q

Cherry angionoma

A

Asymptomatic, bright red to violet macules and papules ranging from pinhead size to larger
⚫ AKA Campbell de Morgan spots
⚫ Acquired vascular proliferation, unknown cause
⚫ More common with age (third decade onwards)
⚫ Benign – no treatment necessary

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21
Q

DERMATOFIBROMA

A

⚫ Benign skin tumour - ?trauma
⚫ Women > men, young adulthood,
immunosuppresed
⚫ Single nodules on an extremity (usually lower leg) – freely moving, firm, usually asymptomatic
⚫ Reassure but refer if uncertain of diagnosis or bothersome
Sarcoma is a differential

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22
Q

SEBACEOUS HYPERPLASIA

A

Benign hair follicle tumour

Enlarged sebaceous glands (oil producing glands) on forehead or cheeks of middle- aged or elderly patients
⚫ Small yellow bumps up to 3mm diameter with central dimple (from hair)
⚫ Easily confused with BCCs
⚫ Prominent vascularisation on dermascopy

More common in immunosuppressed pts
No need for treatment – consider referral if unsure

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23
Q

SEBORRHOEIC KERATOSIS

A

⚫ 90% of people aged 60+ have at least one
⚫ Warty growth with ‘stuck on’ appearance – very variable appearances
⚫ Flat or raised papule or plaque
⚫ Variety of colours and sizes
⚫ Smooth, waxy or warty surface

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24
Q

SKIN TAGS

A

⚫ Skin-coloured or darker, pedunculated lesions (on a stalk) most commonly around neck, groin and armpits
⚫ More common in obese people and those with T2DM
⚫ Cause unknown- benign
⚫ Can be removed with elecsurgery, cryotherapy or ligation

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25
Naevi
⚫ Moles – well defined, congenital lesions ⚫ Appear and develop between age of 2 and 60, very rare to undergo malignant changes ⚫ Can be hairy, raised, skin coloured or pink/red to black/blue ⚫ If it looks suspicious or behaves differently Ie irregular, colour changing– REFER for expert assessment
26
Lipomas
⚫ Slow-growing, benign tumour of adipose tissue ⚫ Fairly common (approx 1 in 1000 people) usually appear between 40-60yrs ⚫ Soft nodule, skin coloured, smooth surface ⚫ If >5cm, fast growing and near thigh/groin – refer to exclude liposarcoma ⚫ Removal for cosmetic reasons if needed Refer for U/S to check for vascularity is concerned for Ca
27
ACTINIC KERATOSIS
Red, scaly patchiness which is usually on old peoples scalp, cheeks and hand Caused by UV damage to the skin Most affected are fair people with blonde hair and blue eyes – almost entirely confined to type I and II Increases with age (UV is cumulative) More common in men (& Australians!) Begin as small rough spots in sun exposed areas, and enlarge over several years to become red and scaly If continued exposure – can progress to SCC (10% chance of one/7.7 becoming malignant within 10 years) Don't always need managing – refer to derm non-urgently
28
BASAL CELL CARCINOMA
Accounts for 80% of skin cancers Slow growing, locally invasive tumours ⚫ Very uncommon in dark-skinned races ⚫ Most common in sun-exposed areas ie: head and neck and in males ⚫ Increases with age – and likely to get more if have one Small, translucent, pearly lesions with raised edges. Can then progress into''rodent ulcer'' Referral should be on a routine basis if needed Only consider 2ww if area is problematic or exceptionally large Can be managed in GP with minor surgery if available If not – refer to derm routinely
29
Basal cell carcinoma treatment
Can be managed in GP with minor surgery if available If not – refer to derm routinely Treatment is either surgical excision, or imiquimod or flourouracil creams Low risk of mets or spread – however, sun exposure and previous malignancy increases risk of other cancers such as SCCs and melanoma Important to remind pts to stay out of the sun!
30
Squamous cell carcinoma
⚫ Malignant tumour that arises from keratinising cells of the epidermis – locally invasive but CAN metastasise ⚫ About 10,000 cases diagnosed in England and Wales every year ⚫ More common in caucasion people, men, and older people ⚫ Linked to UV exposure Typically presents as a non-healing ulcer in sun exposed area (ie head or neck) Can vary considerably Nodule with induration and keratisation, or can just be an ulcerated lesion Can bleed USUALLY ulcerated lesion with hard raised edges
31
Malignant melanoma
Cancerous growth of melanocytes Much less common than BCC or SCC More common in women (legs) than men (trunk) ⚫ Affecting younger age groups (50% under 60) ⚫ Fifth most common cancer in UK (3rd inAus/NZ) ⚫ Lifetime risk UK 1 in 55/56 Usually irregular and has 2 colours Superficial spreading melanoma most common subtype.Also have lentigo maligna, acral lentiginous and nodular (most aggressive)
32
Malignant melanoma risk factors
⚫ Risk factors: ⚫ Naevi- >100 common naevi or >2 atypical, 5-20x chance ⚫ Sun exposure, especially sunbeds before 30y ⚫ Skin type 1 or 2 (black people 20x less) ⚫ Family history ⚫ Higher socio-econominc group
33
abcde of malignant melanoma
⚫ A Asymmetry ⚫ B Border irregularity ⚫ C Colour variation ⚫ D Diameter over 6 mm ⚫ E Evolving (enlarging, changing - inflammation, itching, oozing
34
Eczema
 Also known as dermatitis (although dermatitis is a broader term)  Characterised by dry, itchy and inflamed skin  Not contagious  Very common and increasing incidence – 20% of children and 1 in 12 adults have some form  Types include atopic eczema,contact dermatitis, seborrhoeic dermatitis, discoid eczema, pompholyx, varicose eczema and asteatotic eczema
35
Atopic eczema
 Presentation usually at a young age – itching, red,dry skin  Genetic link – especially in those with family history of atopy – filaggrin  Triggers include stress, diet, contact allergens, irritants, skin infections, animals, abrasive fabrics, temperature changes and inhaled allergens ie: dust mites
36
Diagnostic criteria of eczema
 Must have an itchy skin condition (or report of scratching or rubbing in a child) plus three or more of the following:  History of itchiness in skin creases such as folds of the elbows,behind the knees, fronts of ankles,or around the neck (or the cheeks in children aged 18 months or under).  History of asthma or hay fever (or history of atopic disease in a first-degree relative in children aged under 4 years).  General dry skin in the preceding year.  Visible flexural eczema (or eczema affecting the cheeks or forehead and outer limbs in children aged under 4 years).  Onset in the first two years of life (not always diagnostic in children aged under 4 years).  IF IT DOESN’T ITCH,IT’S VERY UNLIKELY TO BE ECZEMA!!!
37
Potential eczema investigations
 No investigations usually required  IgE and RAST testing simply confirms atopy
38
Emollient - eczema treatment
 These are best applied when the skin is moist but they should also be applied at other times.  They should be applied as liberally and frequently as possible and continual treatment with complete emollient therapy (combinations of cream, ointment, bath oil and emollient soap substitute) will help to provide maximal effect.  Ideally the frequency of application of emollients should be every 4 hours or at least 3-4 times per day.  They should be prescribed in large quantities, with the recommended quantities used in generalised eczema being 500 g/week for an adult and 250 g/week for a child.  Intensive use of emollients will reduce the need for topical steroids.  Education on how to use emollients is essential to ensure maximal rehydration of the skin.  Most patients use far too little emollient!
39
Topical steroid for atopic eczema
TOPICAL STEROIDS ie hydrocortisone  It is recommended that topical corticosteroids for atopic eczema should be prescribed for application only once or twice daily.  Use mild potency for mild atopic eczema, moderate potency for moderate atopic eczema and potent for severe atopic eczema.  Use mild potency for the face and neck, except for short-term (3-5 days) use of moderate potency for severe flares.  Use moderate or potent preparations for short periods only (7-14 days) for flares in vulnerable sites such as the axillae and groin.  Do not use very potent preparations in children, without specialist dermatological advice.  Patients using moderate and potent steroids must be kept under review for both local and systemic side-effects.  Chronic eczema in adults: this often requires a potent steroid together with emollients and allergen avoidance.
40
Topical steroid side effects
 Local side effects may arise when a potent topical steroid is applied daily for long periods of time (months).  Skin thinning (atrophy)  Stretch marks (striae) in armpits or groin  Easy bruising (senile/solar purpura) and tearing of the skin  Enlargedbloodvessels(telangiectasia)  Localisedincreasedhairthicknessandlength(hypertrichosis)  Potent topical steroid applied for weeks to months or longer can lead to:  Periorificial dermatitis (common)  Steroidrosacea  Symptoms due to topical corticosteroid withdrawal  Pustular psoriasis.  Stinging frequently occurs when a topical steroid is first applied, due to underlying inflammation and broken skin.  Veryrarely:Cushing’s
41
Contact dermatitis
 Two types – irritant (common substances) and allergic (uncommon substances) . Irritant occurs when skin contacts known irritants ie solvents, and also frequent hand washing. Allergic is a reaction to ‘normal’ stimulus ie: nickel, rubber etc.  Irritant more common in those with atopy.  Differentiate with careful history taking  Hands most commonly affected, then arms, neck and face.  Not contagious  Symptoms – itching, sore, red skin, blisters and fissures  Diagnosis – clinical, allergic can be confirmed with skin patch testing
42
Contact dermatitis treatment
 Avoid contact with irritants and substances that trigger  Emollient use  Steroid cream  Can use oral steroids if very severe  Antibiotics if secondary infection
43
SEBORRHOEIC DERMATITIS
 Very common – affects up to 50% of population but most don’t know they have it.  Slightly more common in men.  Affects greasy areas ie:scalp,sternal area,face,groin.  Dandruff (v. mild on scalp), cradle cap (babies)  Thought to be triggered by overgrowth of yeast or an over-reaction to it.  Tiredness and stress can trigger; more common in cold weather  Not linked to any underlying disease, although can be more severe in HIV patients and more common in Parkinson’s  Affected areas are red with greasy looking flakes – commonly scalp, eyebrows, ears, chest.  Itching and painful if rashes start weeping – can be very embarrassing.
44
SEBORRHOEIC DERMATITIS treatment
 Treatment is usually needed on a long-term basis  On the scalp: medicated, anti-dandruff shampoos containing agents such as zinc pyrithione, selenium sulphide or ketoconazole can be used regularly.Thick scales can be removed with coconut oil and salicyclic acid overnight.  Elsewhere: anti-yeast creams or ointments are usually effective and can be used safely as long-term treatment.Examples include clotrimazole, miconazole and nystatin.They are sometimes combined with a mild steroid for a few weeks to settle inflammation.
45
POMPHOLYX
 Also known as dishydrotic eczema  Characterised by burning sesnsation followed by small vesicles and blisters on hands and feet – intensely itchy. Then subsquent peeling leaving dry, hard skin.  Unknown causes although stress and heat can play a part. More common in females.  Affectspalms,soles,sidesoffingers, tops of toes. Can cause nail problems (paronychia).
46
POMPHOLYX treatment
 Difficult to treat due to extra horny layer of skin on hands & feet.  Wet dressings – can try dilute potassium permangenate (stains!!)  Cold packs  Emollients +++  Some cases are helped by mild steroids (hydrocortisone 1%) but usually need potent  Specialist advice: ultrapotent topical steroids applied to new blisters under occlusion, and ointments applied during the inflamed dry phase.  Short courses of prednisolone if needed for severe flares
47
DISCOID (NUMMULAR) ECZEMA
 Characteristic round/oval patches. More common in men than women. Rare in children.  Usually worse on arms and legs  Starts as tiny red spots which cluster together and form red, swollen, sometimes moist round patch which then becomes dry and scaly (red target like lesions)  Diagnosis – often take skin scrapings to r/o other pathology
48
DISCOID (NUMMULAR) ECZEMA treatment
 Emollients +++ (even when not dry)  Mild topical steroids no use – must use potent or very potent.  Tacrolimus/pimecrolimus (specialist)  UV light therapy  Oral steroids  Rarely – immunosuppression like azathioprine
49
ASTEATOTIC ECZEMA
 Almost always in over 60s  Cause unknown – could be linked to loss of skin oils, low humidity, hot baths  Appears on shins initially – crazy paving, red scaly dry skin in old people  Clinical diagnosis Treatment same: alleviate factors, emollients, steroid creams
50
Varicose eczema
 Also known as stasis eczema,gravitational dermatitis  Valves in legs don’t work properly, reducing venous drainage & increasing pressure causing damage to overlying skin.  Being overweight, immobility, leg swelling, varicose veins,VTE and previous cellulitis are possible contributory factors.  Appears on lower legs – appearance from dry skin through to thickening, ulcers, and classic eczema appearance Treatment  Emollients! +++  Bandaging and compression stockings  Address underlying issue  No steroids
51
Psoriasis
 Psoriasis is an immune-mediated disease that causes raised, red, scaly patches to appear on the skin.  Skin cells grow at an abnormally fast rate, causing characteristic lesions and scaling of psoriasis  Five types: chronic plaque psoriasis, guttate psoriasis, pustular, erythrodermic, inverse
52
CHRONIC PLAQUE PSORIASIS
 Psoriasis affects approx 1.3-2.2% of people, mostly white people.  Plaque psoriasis accounts for 90% of patients  Men and women equally effected  Can occur at any age, usually before 35, uncommon in children  30% have family history  Environmental factors – drugs, trauma, sunlight  Associated with IBD, metabolic syndrome, increased risk of CVD and lymphoma – unsure why PRESENTATION  Chronic plaque psoriasis is typified by itchy, well-demarcated circular-to-oval bright red/pink elevated lesions (plaques) with overlying white or silvery scale, distributed symmetrically over extensor body surfaces and the scalp.  Fissuring within plaques can occur when lesions are present over joint lines or on the palms and soles.  Gentle scraping accentuates the scale (vigorous scraping causes pinpoint bleeding - Auspitz' sign - pitting of the nails).  The psoriatic lesions are a very distinctive rich, full, red colour.When present on the legs, lesions sometimes carry a blue or violaceous tint.  Remember nail changes!
53
Management of chronic plaque psoriasis
 First-line therapy which includes traditional topical therapies - eg, corticosteroids, vitamin D analogues, dithranol and tar preparations.  Second-line therapy which includes phototherapy, broad-band or narrow-band ultraviolet B light, with or without supervised application of complex topical therapies such as dithranol in Lassar's paste or crude coal tar and photochemotherapy,psoralens in combination with UVA irradiation (PUVA), and non-biological systemic agents such as ciclosporin, methotrexate and acitretin.  Third-line therapy which refers to systemic biological therapies that use molecules designed to block specific molecular steps important in the development of psoriasis, such as the TNF antagonists adalimumab, etanercept and infliximab, and ustekinumab, anti-IL12-23 monoclonal antibody. TOPICAL THERAPIES  Emollients ++++!!  Short term use of potent or very potent topical corticosteroids  Vitamin D analogues (calciprotel/Dovonex) for maintenance  Coal tar  Tarozatene gel (vit A analogue)
54
GUTTATE PSORIASIS
 Small, scattered, round/oval lesions that appear over about a week  Trunk and proximal limbs most affected  Classically appears as first presentation and after an illness eg usually a viral infection  If widespread (>10%) urgent ref to derm for phototherapy  Self-resolves within 3-4/12, but can use topical rx to help interim
55
Inverse psoriasis
 Inverse psoriasis (aka intertrigous or flexural)  Found in skin folds, armpits, breasts etc  Often mistaken for fungal – can coincide  Lacks scale due to moistness  Rx much the same
56
Pustular psoriasis
 Pustular psoriasis  White bumps on plaques, can coalesce to form “lakes” of pus Blister like rash  MEDICAL EMERGENCY
57
ERYTHRODERMIC PSORIASIS
 Diffuse,widespread,severe Blister like red scaly rash all over body  Affects >90% of body  Can be systemically unwell  MEDICAL EMERGENCY
58
URTICARIA
Allergic reaction ie nettle sting reaction ⚫ Commonly known as hives ⚫ Characterised by raised pale or skin-coloured patches surrounded by erythema - “wheals” ⚫ Itchy +++, swelling of the superficial skin layers ⚫ Typically transient so will come and go within minutes to hours ⚫ Can be subdivided into acute or chronic (>6/52).Acute (1 in 6 people) much more common than chronic (1 in 1000).
59
Urticaria treatment
⚫ Consider drugs that can cause reactions specifically NSAIDs/ACEIs ⚫ Management is to soothe itch (calamine lotion) and principally with anti- histamines ⚫ Cetirizine,loratadine and fexofenadine are preferred.Can use up to 4x standard dose. ⚫ Refer if not controlled on max dose or causing significant distress
60
ANGIOEDEMA
⚫ Often co-exists with urticaria ⚫ Characterised by swelling of the deeper subcutaneous tissues, frequently around the mucus membranes of eyelids and lips ⚫ Tends to be more painful than itchy ⚫ Can be chronic or acute
61
Angioedema types and causes
Types/Causes Allergic (1-2hrs after exposure): commonly food, latex, drugs, insect venom Drug reaction (days to months after exposure): most commonly seen with ACE-Is in black people Idiopathic: most cases, cause unknown. ?autoimmune Hereditary: very rare
62
Angioedema treatment
Treatment Treatment is much the same as urticaria with antihistamines Sometimes oral corticosteroids are used and in some specialist cases, anabolics! Severe cases should be referred on – tx can then include immunosuppressants and monoclonal antibodies but under specialist care only
63
Anaphylaxis
⚫ A severe and rapidly developing systemic hypersensitivity reaction ⚫ Often associated with urticaria in reaction to stimulus. Commonly foods (peanuts/shellfish), drugs (penicillin most freq), insect stings (bees/wasps) but can react to a wide range ⚫ Characterised by urticaria, angiodema, hypotension and bronchospasm that is sudden onset and life threatening ⚫ ANAPHYLAXIS IS A MEDICAL EMERGENCY AND REQUIRES IMMEDIATE RECOGNITION AND TREATMENT ⚫ Initially, patients usually develop skin symptoms, including generalised itching, urticaria and erythema, rhinitis, conjunctivitis and angioedema. ⚫ Signs that the airway is becoming involved include itching of the palate or external auditory meatus, dyspnoea, laryngeal oedema (stridor) and wheezing (bronchospasm). ⚫ General symptoms include palpitations and tachycardia (as opposed to bradycardia in a simple vasovagal episode), nausea, vomiting and abdominal pain, feeling faint - with a sense of impending doom; and, ultimately, collapse and loss of consciousness. ⚫ Airway swelling, stridor, breathing difficulty, wheeze, cyanosis, hypotension, tachycardia and reduced capillary filling suggest impending severe reaction.
64
Anaphylaxis management
⚫ Assess as emergency with ABCDEs ⚫ Give high-flow oxygen ⚫ Give adrenaline IM (500mcg for adults and children >12yrs, 300mcg 6- 12yrs, 150mcg <6yrs) into thigh – can repeat doses if no response after 5m ⚫ Get patient flat, call for help, likely to need airway mgmt/intubation ⚫ Cannulate and fluid challenge, warmed NS/Hartmann's 500ml-1L ⚫ Antihistamines such as chlorphenamine (IM or IV) ⚫ Hydrocortisone (IM or IV) after initial resuscitation ⚫ Any out-of-hospital anaphylaxis should be sent to hospital due to the risk of rebound reactions
65
ERYTHEMA NODOSUM
⚫ Likely to be a hypersensitivity reaction and/or a dermatological manifestation of underlying disease ⚫ Characterised by red, tender nodules frequently on the shins. These tend to last 2-6 weeks and can change in consistency to feel fluctuant or tense, and may be associated with joint pains, fever or general malaise ⚫ Most common in younger women aged 20-30,but can affect all ages/sexes
66
ERYTHEMA NODOSUM underlying differential diseases
Bacterial - TB, claymidia, salmonella Viral - EBV, HSV, HIV Fungal infections Sarcoidosis Drug reactions Pregnancy IBD
67
ERYTHEMA MULTIFORME
⚫ Hypersensitivity reaction, caused by an infection in 90% of cases, most commonly HSV.Young men most affected, some familial links. ⚫ Usually begins with lesions on hands and feet, then spread along limbs towards trunk within 24hrs. ⚫ Classic lesions are target lesions, although can take many forms. Target lesions have three colour zones: a central crusted dusky/dark red area, a raised pale pink oedamatous area, and a bright red outermost ring ⚫ Mucous membranes are very rarely affected and if they are, only very mild involvement ⚫ Clinical diagnosis, and treatment usually not required as is self-limiting
68
Stevens-Johnson syndrome and TOXIC EPIDERMAL NECROLYSIS
Life threatening medical emergency SJS is a less severe version of TEN ⚫ Rare skin reactions that cause sheet-like skin and mucosal loss – severe and can be life-threatening dermatological emergencies ⚫ Caused by medication in 75% of cases, infection in the remaining.Antibiotics are the most common (40%) and drugs with longer half-lives seem to be more likely to cause issues ⚫ Unpredictable,anyoneonanymedicationcandevelop,howeveritis100xmore common in HIV patients ⚫ Some genetic risk with certain HLA genotypes ⚫ Very rare – in Europe,approx 2-3 cases per million people per year but serious so needs to be recognised ⚫ Mechanism is not understood ⚫ Usually within 2 weeks of abx therapy (2/12 of anticonvulsant) a prodromal flu-like illness/URTI develops which is followed by: ⚫ Rapid onset of painful skin rash that starts on trunk and extends rapidly onto face and limbs, reaching maximal extent ~4 days. Can be macules, papules, blisters, target lesions. Blisters then merge to form sheets of skin detachment and leave exposed erythematous oozing dermis. ⚫ Mucus membranes and eyes are affected with ulcers – GI problems are common ⚫ The patient will be unwell, in a lot of pain, and likely to be dehydrated ⚫ Mortality is 10% in SJS and at least 30% in TEN (diagnosed by amount of skin loss)
69
WHAT ARE BLISTERS AND LICHEN?
Blisters (or bullae) are accumulations of fluid under, or within, the epidermis Commonly caused by trauma (dodgy shoes!) and burns. Lichen is a symbiotic algae/fungus that commonly grows on trees and gravestones Lichenoid disorders are named because of their flat, scaly appearance – look similar to lichen!
70
LICHEN PLANUS PRESENTATION AND AETIOLOGY
Affects approx 1% of people worldwide More common in 40yrs+ and in women 50% of cases are oral lichen planus T-cell mediated autoimmune disease – unknown which protein they attack Often appears at sites of trauma (Koebners) Shiny, flat, firm plaques with white lines (Wickham striae) – can be intensely itchy Fade over time to leave brown-grey macules. In the mouth – lacy, white pattern across tongue and mucosa Similar looking to psoriasis but wouldn’t flake off when scratched
71
Lichen planus management
Treatment is with steroid cream – often potent to control the itch Tacrolimus can also be used especially where skin-thinning could be a problem (e.g face) Severe cases need derm assessment – can have phototherapy, methotrexate etc
72
LICHEN SCLEROSUS PRESENTATION AND AETIOLOGY
10x more common in women Can present at any age but frequently over 50 (post- menopausal) Common in genital areas but can be elsewhere on body – typically under breasts, wrists, inner thigh, buttocks and armpits 5% of people can develop SCC of vulva/skin/penis White, shiny, thin tissue- paper appearance of skin Can be itchy and lead to skin breakdown Can lead to vulvovaginal atrophy, clitoral phimosis, and constipation if anal area is affected
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LICHEN SCLEROSUS DIAGNOSIS AND MANAGEMENT
Diagnosis usually clinical – fairly obvious pathology to see – however NICE recommends referring all cases to dermatology Can be sent for biopsy and histopathology,especially if there is a suspicion of cancer Management is with very potent steroid, usually clobetasol proponiate 0.05% General lifestyle measures such as gentle washing, avoiding bikes/horseriding, avoid tight underwear, use emollients Can be embaressing and difficult as effect on sex life etc
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BULLOUS PEMPHIGOID PRESENTATION AND AETIOLOGY
Blistering condition - red, sore, bulging blisters all over the body Autoimmune, subepidermal blistering condition Occurs later in life – usually in people 80+ (looks and presents like eczema but they’ve never had eczema before so tends to be this instead) More prevalent in those with neurological disease ie dementia or Parkinson’s A variation affects pregnant women Initial presentation is variable but itch is common, followed by rash which can appear eczematous or urticarial Large, tense, fluid-filled bullae then appear especially in folds and on abdomen Can have oral involvement in 25% of cases
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BULLOUS PEMPHIGOID DIAGNOSIS AND TREATMENT
Diagnosis is clinical but should be referred to dermatology Fluid from blisters can be tested and immunoflouresced Disease often self-limiting within 1-5 years and leaves no scarring Aims of tx – reduce current blisters, prevent new blisters, minimal meds as elderly pts Very mild cases can use steroid creams Oral steroid such as prednisolone often used initially alongside tetracycline abx and supplementation for vit D/calcium Immunosuppressants if needed
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PEMPHIGUS What is it? Aetiology Presentation
⚫ Autoimmune disease Differentiated from pemphigoid due to where the blisters form – these are in the epidermal layer rather than subepidermal – have thinner roofs and burst easier ⚫ Subtypes Permphigus vulgaris most common subset (70%) - affects mucosa Pemphigus foliaceus is only in the skin and associated with antibodies to DSG1 (desmoglein) Most common in ages 30-60yrs Less common than BP in the UK More common in Jewish populations and those of Indian descent Could be triggered by environmental factors Often appears in mouth first (in PV) Thin walled, fluid-filled clear flaccid blisters burst easily to leave erosions/ulcers Painful and slow to heal, but not normally itchy
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PEMPHIGUS DIAGNOSIS & MANAGEMENT
⚫ Refer to dermatology and/or oral medicine ⚫ Biopsy taken, histopathologically analysed and direct immunoflourescence used to confirm – can also use IDIF look for antibodies in blood ⚫ Oral corticosteroids mainstay of tx (their use has improved mortality from 99% to 5%!) ⚫ Immunosuppressants can be used to minimise steroid use ⚫ Plasmapheresis in very extreme cases
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STAPHYLOCOCCAL SCALDED SKIN SYNDROME
⚫ Red, wrinkled, blistered skin (looks like a burn) caused by exotoxins released by S. aureus ⚫ Usually occurs in children, especially neonates ⚫ Send to hospital – needs tx with IV flucloxacillin Also use simple analgesa and skin care as is fragile
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What is a good antibiotics used to treat skin conditions
flucloxacillin
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DERMATITIS HERPETIFORMIS
⚫ Not due to viral infection–named because blisters appear in clusters. Autoimmune. ⚫ Linked to coeliac disease(over90%) ⚫ Most common in Caucasian people, males 2:1 Symmetrical distribution, intensely itchy but often not much to see ⚫ Diagnosis is with skin biopsy showing IgA Treatment is definitive with lifelong gluten-free diet however there is a medication called Dapsone which resolves rash whilst waiting for diet to take effect