Comprehensive Dermatology Notes
Comprehensive Dermatology Notes
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The Basics
1. Describing the Lesion
a. Location & Distribution
b. Colour
c. Type (Primary morphology)
d. Configuration (Secondary morphology)
e. Texture/secondary changes
f. Other signs
2. Location & Distribution
a. Single or multiple
b. Localised or generalised
c. Symmetrical or asymmetrical
d. Flexure or extensor
e. Body parts – scalp, face, trunk, limb etc
f. Sun-exposed or protected skin
3. Colour
a. Erythematous – inflammation/infection/vascular
b. Orange – hypercarotenaemia
c. Yellow – jaundice, xanthelesma, xanthoma
d. Purple – cutaneous haemorrhage, vasculitis, haemangiomas, dermatoyositis (heliotrope colour
around eyelid)
e. Blue, silver, grey – drug/metal deposition, ischemia, deep dermal naevi
f. Black – naevi, melanoma (melanocytic), ecshars (dead skin from infarction), arterial
insufficiency, vasculitis
g. Hyperpigmented
h. Hypopigmented
4. 4. Types (primary morphology)
a. Macules : flat, <1cm
b. Patch : flat, >1cm
c. Papule : palpable, < 0.5cm
d. Nodule : palpable, > 0.5cm
e. Plaque : palpable, flat-topped, > 1cm
f. Vesicle : fluid-filled blister, < 0.5cm
g. Bulla : vesicle > 0.5cm
h. Pustule : small collection of pus
i. Abscess : collection of pus, >1cm
j. Wheal/urticaria : transient dermal edema often surrounded by zone of erythema
k. Burrow : tunnel
l. Erosion : loss of part or all of epidermis
m. Ulcer : loss of epidermis & part of dermis
n. Petechiae : punctate foci of haemorrhage
o. Purpura/ecchymoses : larger area of haemorrhage
p. Telangiectasias : foci of small, permanently dilated blood vessels
5. Configuration (secondary morphology)
a. Linear : straight line
b. Serpiginous : linear, branch & curving elements
c. Annular : rings with central clearing
d. Target (bull’s-eye or iris) lesions : rings with central duskiness e.g. erythema multiforme
e. Discoid/nummular : circular or coin-shaped
f. Umbilicated : central indentation e.g. molluscum contagiosum
g. Grouped : e.g. herpes simplex
h. Bizzare : e.g. dermatitis artefacta
i. Herpetiform : grouped papules/vesicles
j. Zosteriform : clustered in dermatomal distribution
6. Texture
a. Scales : keratin presents as flaking
b. Crust : dried serum and exudate
c. Atrophy : thinning, loss of normal skin markings
d. Lichenification : thickening, prominent skin markings due to repeated scratching or rubbing
e. Scarring : fibrosis replacing normal skin, may be hypertrophic, raised, keloid
f. Excoriation : scratch marks causing erosions/ulcers
g. Verrucous : irregular, pebbly, or rough surface e.g. warts and seborrheic keratoses
URTICARIA
1. Describe
a. Multiple generalised erythematous wheals over the
forearm
2. Diagnosis
a. Urticaria
3. Causes
a. Shellfish, strawberry
b. Penicillin
c. Sweating (cholinergic)
d. Heat, water, cold, light
4. Investigation
a. Skin prick test
b. Radioallergosorbent test (RAST) - serum Antibody
5. Treatment
a. Avoid triggers
b. Antihistamine eg loratadine
ii.
- Napkin psoriasis
- Napkin irritant contact dermatitis (below)
- Napkin candidiasis with satellite lesions
Napkin seborrhoeic dermatitis
1. Describe
a. Erythematous macerated (softened) skin confined to
area of napkin, sparing the skinfold
2. Diagnosis
a. Napkin irritant/ammoniacal dermatitis
3. Cause
a. Prolonged contact with urine and feces in the napkin
4. Treatment
a. Zinc oxide ointment → Promote drying of wet, oozing
lesions
b. Frequent change of diapers
1. Describe
a. Multiple erythematosus discoid mixed of papule and
plaque over the back
2. Diagnosis
a. Discoid/nummular eczema
3. Causes
a. Triggered by
i. Minor skin trauma eg insect bites
ii. Drugs eg interferon, ribavirin
4. Investigation
a. Skin scrape TRO fungal infection
5. Treatment
a. Strong corticosteroids
b. Others same as childhood atopic
1. Describe
a. Generalised erythematous skin changes with dilated
veins and mild hyperpigmentation over the gaiter area
2. Diagnosis
a. Varicose eczema/stasis dermatitis/gravitational
eczema
3. Investigation
a. Duplex ultrasound
b. Skin scrape
4. Treatment
a. Leg elevation
b. Compressive stocking
c. Pentoxifylline - venoactive drugs
d. Surgical management - high strip, ligation,
endovascular radio/thermal ablation
1. Describe
a. Multiple vesicular erythematous skin lesion over the
palmar aspect of the left hand and fingers
2. Diagnosis
a. Pompholyx (itchy vesicle on the palm and soles)
b. aka dyshidrotic eczema
3. Investigation
a. Vesicular fluid swab for C+S
b. Skin prick test
c. Radioallergosorbent test (RAST)
d. Patch testing
4. Treatment
a. Conservative
i. Hygiene
ii. Avoid allergen
iii. Avoid rubbing, scraping
b. Topical
i. Corticosteroid
ii. KMNO4 - drying agent
iii. Coal tar - for itchiness
c. Systemic
i. Steroid
ii. Antihistamine eg loratadine, cetirizine
1. Describe
a. Dry scaly skin with yellow crust over the finger with a
linear fissure
2. Diagnosis
a. Chronic hand eczema with hyperkeratosis and
fissuring
3. Investigation and treatment: as above
1. Describe
a. Crazy paving - dry superficial fissure
b. Dry cracked and polygonal fissured skin with
irregular scarring (asteatotic)
2. Diagnosis
a. Asteatotic eczema/eczema craquele/xerotic eczema)
@ Skin is abnormally dry, itchy and cracked
3. Cause
a. Commonly found in elderly
b. Steroid usage can cause skin thinning which predisposes
to this condition
c. Worsen by winter, frequent bathing, central heating ←
caused dry skin
4. Investigation
a. ???
5. Treatment
a. Oil-based emollients
PSORIASIS
1. Plaque
2. Erythrodermic - medical emergency
3. Pustular
4. Flexural
5. Guttate (raindrop)
Onycholysis
Subungual hyperkeratosis
iii.
iv. Scalp - extend beyond hair line
v.
b. Nail
i. Onycholysis (ddx - trauma, onychomycosis,
hyperthyroidism)
ii. Subungual hyperkeratosis
iii. Yellowing of nail
Pitting iv. Pitting
c. Joint (5-10%)
i. Seronegative polyarthropathy:
ii. Symmetrical arthritis
iii. Asymmetrical arthritis
iv. DIP dominant
v. Spondylitis
vi. Arthritis mutilans
d. Eye
i. Uveitis
2. Treatment
a. Conservative
i. Reduce stress, avoid sun and skin trauma
b. Topical
i. Emollients
ii. Coal tar – plaque, guttate, scalp, flexures
iii. Keratolytic eg salicylic acid – reduce scalings
iv. Steroids – only for scalp & flexures
v. Vitamin D analogue e.g. calcipotriol –
suppress plagues, also useful in flexures
c. Phototherapy
i. Goekermann regime:
1. UVB + tar
ii. UVB – 2-3x weekly
iii. PUVA (psoralen + UVA)
iv. REPUVA (retinoids + psoralen + UVA) –
retinoids useful for abnormal keratinization
d. Systemic
i. 5-30 mg po methotrexate once/weekly –
generalized pustular psoriasis, erythroderma,
psoriatic arthropathy). SE: hepatic fibrosis
ii. Azathioprine - steroid sparing therapy
iii. Biological agents (infliximab/etanercept)
iv. Systemic steroid - but don’t stop abruptly
otherwise will cause flare up
1. Describe the lesion?
a. Single well-demarcated salmon-pink plaque with
silver scaling over the extensor surface of the elbow
2. Diagnosis?
a. Plaque psoriasis (psoriasis vulgaris)
3. Possible causes?
a. Genetic HLA-CW6
b. Trigger factors (see notes)
i. Physical trauma
ii. Infection
iii. Stress
iv. Alcohol
4. Sites of predilection: scalp, extensor surface, umbilicus
5. Investigation
a. Skin scrape - TRO fungal infection
6. Treatment
a. Refer above
1. Diagnosis
a. Flexural psoriasis (inverse psoriasis)
2. Description
a. Well demarcated pinkish glazed lesions, non-scaly
3. Affected region: axillae, groin, perianal creases, submammary
folds
1. Diagnosis
a. Guttate/Raindrop-like psoriasis
2. Describe
a. Drop-like lesions, salmon-pink papules
with fine scales
b. Explosive eruptions of small oval plaques
3. Affected area: trunk & limbs
4. Often appear 2 weeks after strep sore throat and resolves
within 4/12
1. Diagnosis
a. Pustular psoriasis
2. Affected area: palms, soles
3. Describe:
a. Well demarcated scaling + erythema
b. Yellow/green pustules
1. Diagnosis
a. Erythrodermic (confluent/brittle) psoriasis
2. Medical EMERGENCY - serious, life threatening
3. Describe
a. Plaques merge over widespread areas
4. Causes
a. Inappropriate use of Dithranol (psoriasis medication)
b. Sudden withdrawal of potent steroids
5. DDx
a. TEN, exfoliative erythroderma,
6. Complications
a. Loss of heat, water, electrolytes, iron, protein
b. Heart failure, secondary infection
ACNE
1. Acne vulgaris
2. Rosacea
a.
b. Comedones - open or closed
c. Papules
d. Pustules
e. Nodules
f. Cysts
g. Scars - atrophic or hypertrophic or keloid
1. Describe the lesion?
a. Multiple polymorphic erythematous papules and
pustules on the left cheek with greasy/oily skin
2. Diagnosis?
a. Acne vulgaris (don’t confuse with “verruca vulgaris”, which
are common warts - viral HPV)
3. Causes:
a. FHx, hormonal, OCP, cosmetics, contact with oil,
weather and stress
4. Pathogenesis?
a. Hypertrophic sebaceous gland
b. Comedogenesis
c. Proliferation of propionibacterium acnes
d. Inflammation (breakdown of sebum by bacteria)
5. Affected sites:
a. face, chest, back and shoulder + upper arms
Type of acnes
1. Infantile acne: > males, clears spontaneously, but may last for some
years, in response to maternal hormone
2. Acne excoriee: young women, related to squeezing and picking
3. Acne conglobata (nodulocystic): severe form of acne characterised
by burrowing abscesses, sinuses and scarring
4. Chloracne: may be an occupational acne
5. Drug induced acne/ acne medicamentosa: steroids
(topical/systemic), lithium, androgens, and certain types of COCP
6. Acne mechanica: a “physical” type of acne eg due to occlusion at the
back of a wheelchair user or on a violinists chin
Treatment based on severity
Available drugs:
- Topical retinoids
- Topical benzoyl peroxide
- + oral AB (doxycycline) for 3-6 months
- Not suitable for pregnant women
- ++ oral isotretinoin (reduce sebum, inhibit hyperkeratosis,
anti-inflammation) for 4/12
- Not suitable for pregnant women
- Can only be prescribed by dermatologists
b.
c. Telangiectasia of the face
6. Causes
a. Rule out medications, occupational exposure
b. Worsen by spicy food and alcohol
7. Treatment
a. Topical / oral antibiotics eg metronidazole (Metrogel)
or doxycycline
b. Anti-inflammatory gel eg azelaic acid
BACTERIAL INFECTION
1. Folliculitis, Furuncle, Carbuncle
2. SSSS
3. Impetigo
4. Ecthyma
5. Erysipelas
6. Cellulitis
7. Lyme disease
1. Describe the lesion?
a. Multiple pustules with erythematous surrounding
skin in an area of rich hair distribution e.g. legs
2. Diagnosis?
a. Folliculitis
3. Causative organism → SA
4. Common sites: buttocks & thigh
5. Treatment (self limiting)
a. Topical antibiotics (fusidic acid, mupirocin)
b. **Oral flucloxacillin for SA
c. Antiseptic washes (povidone iodine, chlorhexidine)
a.
5. Treatment?
a. Early treatment is a 14 to 21 day course of oral
antibiotics :
i. Doxycycline (tetracycline) for adults
ii. Cefuroxime and amoxicillin younger
children, and women who are nursing or
breastfeeding.
VIRAL INFECTION
1. Common warts (verruca vulgaris)
2. Flat warts (verruca planae)
3. Plantar warts (verruca palmoplantar)
4. Filiform warts
5. Condyloma acuminata - HPV
6. Molluscum contagiosum - pox virus
7. Chicken pox - VZV
8. Shingles - VZV
9. Herpes zoster ophthalmicus - VZV
10. Herpes simplex labialis - HSV1/2
11. HFM disease - coxsackie virus
1. Diagnosis
a. Filiform (threadlike) wart
Herpetic whitlow
Types
b.
4. Treatment
a. PO griseofulvin 20-25 mg/kg/day x4-6 week
Alternative: oral itraconazole/terbinafine
b. Selenium sulfide shampoo to reduce spread of spores
1. Describe
a. Opaque, thickened, brittle nails
2. Diagnosis
a. Tinea unguium (onychomycosis)
3. Treatment
a. Topical clotrimazole or terbinafine
b. PO antifungal eg itraconazole/terbinafine
1. Describe
2. Diagnosis
a. Tinea incognito (unrecognised tinea infection due to
modification with corticosteroid treatment)
3. Clinical features
a. Which leads to skin atrophy, purpura and telangiectasia
b. Lesions are enlarging and persistent
c. Common sites: Groins, hands, face
d. Compared to tinea corporis:
○ Less raised margin, less scaly
○ More pustular, extensive and irritable
4. Investigations
a. Skin scrapings for microscopy and culture (few days
after stopping all creams)
b. Skin biopsy (to find out causative organism)
5. Treatment
a. Symptomatic relief of itching (mild calamine lotion)
b. Stop topical steroid or calcineurin inhibitor
c. Topical ketoconazole
1. Describe
a. Multiple boggy-looking pustules encircled by
erythematous well-circumscribed patches on the scalp
2. Diagnosis
a. Kerion
3. Clinical Features
a. Presents as an abscess, tender and fluctuant with marked
inflammation
b. Common sites: Scalp, face (beard area), limbs
c. If fungal cause: Hairs plucked out easily and no pain
d. If bacterial cause: Hair is stuck and painful to pluck
e. Regional lymphadenopathy
f. Can get unwell
g. May be followed by widespread itchy eczema-like rash
(dermatophytid)
h. Contagious!
4. Investigations
a. Scalp scrapings and hair sample for microscopy and
fungal culture
b. Bacterial swab (Secondary bacterial infection common
5. Treatment
a. Oral ketoconazole 6-8/52
b. Ketoconazole shampoo to reduce risk of spread to
others
c. Abx if bacterial infection
c.
d. Fungal culture
7. Treatment?
a. Topical is 1st line -clotrimazole/ketoconazole cream
daily for 1-4 weeks
b. Selenium sulphide 2% shampoo (or ketoconazole or
zinc pyrithione) – apply daily, wait 10 mins and rinse,
1-4 weeks
c. Oral medications – fluconazole, itraconazole – causes
hepatotoxicity, drug interactions, GI side effects, CCF
d. If relapse, maintenance by using shampoo 1-2x per
week
1. Describe?
a. There is a cutaneous serpiginous erythematous lesion
seen over the sole
2. Diagnosis?
a. Cutaneous larvae migrans
3. Investigation
a. Clinical diagnosis
4. Treatment
a. po albendazole 400 mg BD for 3 days
DERMATOLOGICAL EMERGENCIES
1. Toxic shock syndrome
2. Angioedema
3. Exfoliative erythroderma
4. Necrotising fasciitis
5. Meningococcemia
6. SJS
HYPERPIGMENTATION
1. Melasma
1. Describe
a. Hyperpigmentation over the face sparing the
nasolabial fold
2. Diagnosis?
a. Melasma (overstimulation of melanocytes by female
sex hormone to produce melanin in response to sun
exposure)
b. May be exacerbated by pregnancy
3. Investigation
a. Wood lamp examination - can see excess melanin
4. Treatment
a. Prevent sun exposure: sunblock (reapply 2 hourly and
wide brim hat)
b. Rule out post-inflammatory hyperpigmentation
MISCELLANEOUS
1. Basal cell carcinoma
2. Lichen planus
3. Alopecia areata
4. Strawberry naevus
5. Erythema Nodosum
6. Pityriasis (alba, rosea, versicolor, capitis)
7. Vitiligo
8. Sunburn
9. Dermatomyositis
10. HSP
11. Oral hairy leukoplakia
12. Porphyria
13. Bullous pemphigoid
1. Description
a. Hyperpigmented rough nodular nodular papule at the
base of the ear with contracted surrounding skin
b. aka “rodent ulcer”
c. Have a roll up/everted edge
d. Telangiectasia, pearly with ulceration
2. Sun exposure
3. Refer to dermatologist
1. Describe - 5P
a. Polygonal shape
b. Pruritic - u can’t c this -> but you can see his face ‘the
cannot tahan must scratch NOW’ look.
c. Purple
d. Papule (multiple)
e. Plaques
2. Diagnosis?
a. Lichen planus - thickening prominent skin
3. Seen in the mucosa → Lacey looking white streaks-lichen striae
a. Eg of scenario: 30 year old man presents with itchy
purple papules on his wrists and fingers and in his
mouth with overlying white reticulate appearance.
4. Treatment
a. Potent steroids - methylprednisolone
1. Describe
a. Patchy, normal looking skin non scarring area of hair
loss
2. Diagnosis?
a. Alopecia areata, ddx: SLE
3. Investigate by pulling → some hair at edges come out easily
(exclamation mark broken hair)
4. Can have nail pitting, hypopigmented skin
5. Autoimmune disease
6. May treat with intralesional steroids to suppress the
autoantibodies
1. Describe
2. Diagnosis?
a. Strawberry naevus (benign tumour of blood vessels)
3. Self limiting but gets worse first before it gets better (will be
gone by 8 years old?)
4. If it gets too big, vision can be lost due to amblyopia
1. Describe the lesion?
a. Multiple symmetrical mildly erythematous (painful) ill
demarcated nodules, on the anterior lower limbs.
2. Diagnosis?
a. Erythema nodosum
3. Cause and risk factors?
a. Common: strep pharyngitis, TB and sarcoidosis, IBD,
b. Other possible causes.
c.
4. Pathophysiology
a. Inflammation of subcutaneous fat
5. Clinical features?
a. Tender nodules on bilateral shins
b. More common in women
6. Treatment?
a. Resolves without scarring after 2-8 weeks
b. Self limiting
c. NSAIDs, corticosteroids (2nd line)
7. Characteristics of different types of erythema.
1. Describe the lesion?
a. Multiple hypopigmented well demarcated
irregularly-shaped patches on the face
2. Diagnosis?
a. Pityriasis alba (dry white patches)
3. Ddx?
a. Vitiligo
b. Tinea versicolor.
4. Cause?
a. Idiopathic
5. Risk factors:
a. Poor hygiene, sun exposure, humidity
b. Atopic dermatitis, dry skin
c. Children
d. May be associated with puberty
6. Clinical features?
a. Non-contagious and benign
b. Occuring on the cheeks
c. Does not fluorescence under Wood’s lamp
d. Not itchy
7. Treatment?
a. Self limiting
b. Moisturising cream
c. Topical steroids (hydrocortisone)
8. Prevention
a. Avoid exposure to sunlight
1. Diagnosis?
a. Pityriasis capitis = seborrheic dermatitis (please refer
above)
From google:
- Seborrhoeic dermatitis is a form of pityriasis as it relates to the activities of the yeast
Pityrosporum of Malassezia (malassezia furfur, pityrosporum ovale, bottle bacilli).
- Dandruff (Pityriasis simplex capitis) is the mildest form of seborrhoeic dermatitis.
1. Describe
a. Heliotrope- coloured erythema (Gottron’s papules over
the knuckles)
2. Diagnosis : dermatomyositis (pathognomonic!)
a. Diffuse, dusky red and purplish rash seen on the
upper eyelids and covering the whole face. May
become scaly and ulcerate
b.
1. Describe
a. Crops of petechiae over both legs
2. Dx
a. HSP
b. Meningococcal
3. Clinical manifestations for HSP
a. Palpable purpura without thrombocytopenia and
coagulopathy
b. Arthritis/arthralgia
c. Abdominal pain
d. Renal disease
4. Ix:
a. Skin biopsy for IgA
b. Normal PT and apTT (to differentiate this from
purpura due to thrombocytopenia or coagulopathy)
c. FBC: normochromic normocytic anaemia
d. High ESR
1. Describe
a. Fluid-filled bullae on index finger, deep ulcers and
superficial erosions on the left dorsum of hand
b. Other sites: Sun-exposed areas eg face, dorsum of
feet, forearm and legs
2. Dx:
a. Porphyria cutaneous tarda
b. Porphyria - a group of disorders that result from a buildup of natural
chemicals that produce porphyrin in your body. Porphyrins are essential
for the function of hemoglobin.
3. Natural history
a. Skin fragile → formation of tense vesicles/bullae + erosion of skin
b. Associated with : alcohol abuse, DM, oestrogen, NSAID, hep C, HIV
4. Ix:
a. Urinary tests: ↑ uroporphyrinogen
i. Coral pink fluorescence under Wood’s lamp
b. Blood tests: ↑ porphyrins, possibly abnormal LFTs
5. Tx
a. Avoid susceptibility factors and excessive sunlight
b. Phlebotomy to reduce iron
c. Hydroxychloroquine or chloroquine → Form water
soluble complexes with porphyrin which can be
excreted via kidneys
1. Describe
a. Localised multiple bullaes with surrounding
ill-defined erythema and several erythematous erosive
macules.
2. Diagnosis
a. Bullous pemphigoid
3. Causes
a. Autoimmunity against epithelial basement membrane
(IgG is produced)
4. Features
a. A prodromal stage with formation of urticarial lesions
may occur weeks to months before onset of blistering.
b. Intensely pruritic lesions, possibly hemorrhagic, heal
without scar formation
c. Distributed on palms, soles, lower legs, groin and
axillae
d. Usually 60-80 years old
e. Heals without scarring
5. Ix
a. Histology and immunochemistry:
i. Subepidermal clefting and blistering
ii. Deposition of linear IgG and C3 along the
dermoepidermal junction
6. Tx
a. High-dose corticosteroids (prednisolone)
b.
c. Culture with selective media
Picture 3 6. Management
a. IM Ceftriaxone 500mg stat + oral azithromycin 1g stat
b. If PID::
IM Ceftriaxone 500mg stat +
Oral doxy 100mg bd +
Oral metronidazole 400mg tds 14 days
c. Contact tracing
d. Avoid sex until both partners complete treatment