Dermatology Flashcards

1
Q

Define psoriasis

A

A chronic autoimmune inflammatory skin condition characterised by hyperproliferation of keratinocytes causing scaly, erythematous, circumscribed papules with a silver scale

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2
Q

Summarise the aetiology of psoriasis and the risk factors of psoriasis

A

Aetiology is unknown
Genetic component - FHx

Precipitating factors:
Stress
Smoking
Infection
Alcohol
Skin injury
Medication

Guttate psoriasis - streptococcal sore throat

Palmar-plantar psoriasis - smoking, middle-aged women, autoimmune thyroid disease

Generalised pustular psoriasis - hypoparathyroidism

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3
Q

Summarise the epidemiology of psoriasis

A

Mean age of onset 28 years old
Equal in men and women
Affects 1-2% of the population

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4
Q

What are the presenting symptoms of psoriasis?

A

AUSPITZ SIGN - Pinpoint bleeding with removing scales
Skin lesions may develop at sites of trauma/scars (Koebner phenomenon)

Plaque psoriasis (most common type):
Itchy
Well circumscribed purple/red/salmon flattened areas of elevation
White/silver scales
Found on scalp and extensors
Dry flaky skin
Painful

Guttate psoriasis:
Itchy, red small raindrop plaques on back
Following strep throat infection

Pustular planto-palmar:
Small fluid filled pustules on hands and feet

Flexural:
Red, shiny itchy rash found in skin folds (axilla, groin, perianal, under breast

Erythrodermic:
Systemic body redness and inflammation
Painful and itchy

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5
Q

What are the signs on physical examination of psoriasis?

A

Nail signs:
Oncholysis (nail falling off nail bed)
Pitting
Subungal hyperkeratosis - scaling under nail

Signs of psoriatic arthritis:
Asymmetrical oligoarthritis
Symmetrical polyarthritis
Distal interphalangeal joint predominance 
Arthritis mutilans 
Psoriatic spondylitis

Plaque psoriasis - symmetrical, well-demarcated erythematous plaques with silvery scales over extensor surfaces (knee, elbows, scalp, sacrum)
Flexural psoriasis - red, shiny, less scaly plaques in axilla, groins, perianal and genital skin
Guttate psoriasis - small drop-like lesions over trunk and limbs
Palmoplantar psoriasis - erythematous plaques with pustules on palms and soles

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6
Q

What are the appropriate investigations for psoriasis?

A

Usually a clinical diagnosis which requires no investigations
Skin biopsy can confirm diagnosis

Guttate psoriasis: anti-streptolysin-O titre, throat swab
Flexural psoriasis: skin swabs to exclude candidiasis
Nail clipping analysis for onychomycosis (fungal infection)
Joint involvement analysed by checking for rheumatoid factor and radiographs

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7
Q

Define herpes simplex virus

A

Herpes simplex virus is a enveloped, double stranded DNA virus
Infection with HSV-1 or HSV-2 can cause oral, genital, and ocular ulcers. The primary episode occurs during initial infection with HSV, in which the host lacks an antibody response.

HSV-1: mainly oral herpes herpes
HSV-2: mainly genital herpes
HHV-3: varicella-zoster virus - chickenpox and shingles

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8
Q

Summarise the aetiology of herpes simplex virus

A

HSV1 causes herpes labialis (cold sores)
HSV2 causes genital herpes
HSV are large, enveloped, double stranded DNA viruses

HSV-1 and HSV-2 are acquired at mucosal surfaces or at breaks in the skin. The virus replicates in the epidermis, then infects sensory or autonomic nerve endings and travels by retrograde axonal transport to sensory ganglia.
In the latent phase HSV lives in trigeminal ganglia (face sensory neuron cell bodies) and sacral ganglia (genital sensory neuron cell bodies)
Periodic reactivation of the virus produces lytic replication when the virus travels by anterograde transport down axons to the mucosal or cutaneous surface

Reactivation triggers:
Stress
Skin damage
Viral infection

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9
Q

Summarise the epidemiology of herpes simplex virus

A

Infection most commonly acquired during childhood
Seropositivty increases with age
Prevalence of HSV1 and HSV2 higher among women
Very common

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10
Q

What are the presenting symptoms of herpes simplex virus

A
Herpes labialis - cold sores
Painful sores in the genital area 
Itchiness 
Dysuria
Vaginal discharge
Fever 
Headache 
Flu like prodrome for HSV2
Gingivostomatitis - dry crusting sore of mouth
Sore throat
Keratoconjuncitivitis:
Red, painful inflammed eye
Sensitivity to light
Tearing
Blurring of vision
Herpetic whitlow - rash on fingertip
Tingling sensation

Immunocompromised patients may have more severe, prolonged ulceration of the genital or oral mucosa than immunocompetent patients.

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11
Q

What are the signs on physical examination of herpes simplex virus?

A
Fever
Pharyngitis
Lymphadenopathy
Bilateral tender inguinal lymphadenopathy 
Multiple tender 1-2 cm erythematous ulcerations
Oedematous cervix
Pustules 
Clear discharge
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12
Q

What are the appropriate investigations for herpes simplex virus?

A

Mainly clinical diagnosis based on appearance of blisters

Viral culture - detect HSV
HSV PCR - positive
Type-specific serological IgG assay: positive antibody to HSV1 or HSV2

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13
Q

Define lipoma

A

A slow growing, benign tumour composed of adipose tissue, usually found in the subcutaneous tissues particularly of the trunk and proximal limbs. They form well-circumscribed, lobulated lesions composed of adipocytes which are demarcated from surrounding fat by a thin, fibrous capsule

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14
Q

Summarise the aetiology of lipoma

A

Mostly idiopathic

Hereditary:
Familial multiple lipomatosis
Gardner’s syndrome

Madelung’s disease - benign symmetric lipomatosis on head, neck, shoulders - MEN WITH HEAVY ALCOHOL CONSUMPTION
Dercum’s disease - painful lipomas on trunk, shoulders, arms and legs - MIDDLE AGED WOMEN
MEN 1

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15
Q

Summarise the epidemiology of lipoma

A

1% of population
Occur at any age
Most common between 40-60 years old

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16
Q

What are the signs and symptoms of lipoma?

A
SOFT, MOBILE, SUPERFICIAL MASS
Usually painless
Cutaneous mass <5cm diameter
Well circumscribed lesion
Separated from surrounding fat by thin, fibrous capsule
Skin coloured
Smooth normal surface
Soft/doughy feeling
Fluctuant
NOT transilluminate

GI obstruction or bleeding if lipoma found in GI tract

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17
Q

What are the appropriate investigations for lipoma?

A

Mainly a clinical diagnosis
Can use CT/MRI/USS if doubt about diagnosis - show discrete, encapsulated, homogeneous mass with similar density to normal fat
Biopsy - histology consistent with lipoma

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18
Q

Define erythema nodosum

A

A common type IV hypersensitivity reaction leading to inflammation of subcutaneous fat, resulting in raised tender purple nodules often over the shins.

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19
Q

Summarise the aetiology of erythema nodosum

A

25% of cases have no identifiable cause

Infection:
Strep pyogenes (MOST COMMON CAUSE)
Tuberculosis
HIV
Chlamydia
Leprosy
EBV
Histoplasmosis

Systemic inflammation:
IBD
Sarcoidosis
Behcets disease

Drugs:
Sulphonamides
Amiodorone
Oral contraceptives

Pregnancy

Malignancies:
Haematological malignancies
Carcinoid tumours
Pancreatic cancer

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20
Q

Summarise the epidemiology of erythema nodosum

A

Peaks between 20-30 years old
More common in females
Associated with pregnancy

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21
Q

What are the presenting symptoms of erythema nodosum?

A

Bilateral, tender, red/purple erythematous nodules often on the shins
Lesions appear for 1-2 weeks and leave bruise-like discolouration as they resolve
Lesions do not ulcerate and resolve without atrophy or scarring
May be associated with fever, arthralgia
Fatigue
Anorexia
Weight loss

Symptoms of underlying cause:
GI symptoms (change in bowel habit, blood in stool, abdominal pain) - IBD, Behcets
Cough and SOB - TB

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22
Q

What are the signs on physical examination of erythema nodosum?

A

Bilateral, poorly defined, red/purple dome-shaped nodules most commonly on the shins
Occasionally appear on the thighs and forearms
Nodules are tender to palpation
Low-grade pyrexia
Joints may be tender and painful on movement

Signs of underlying CAUSE

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23
Q

What are the appropriate investigations for erythema nodosum?

A

Biopsy if uncertain of diagnosis

Investigations to identify the cause

Bloods:
FBC, ESR, CRP - suggestive of infection (often a leukocytosis)
Serum ACE - raised in sarcoidosis
Anti-streptolysin-O titres - check for streptococcal infection)
m ACE (raised in sarcoidosis)

Throat swab and cultures - check for streptococcous

Mantoux/Head skin testing - for TB

CXR - check for bilateral hilar lymphadenopathy or other evidence of TB, sarcoidosis or fungal infections

If suspect IBD, faecal calprotectin, colonoscopy

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24
Q

Define erythema multiforme

A

An acute hypersensitivity reaction often due to infections, mainly HSV and mycoplasma, leading to skin and mucosal inflammation. It is characterised by target lesions.

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25
Q

Explain the difference between erythema multiforme minor and major

A

Erythema multiforme minor NO mucosal involvement

Erythema multiforme major has 2+ mucosal sites involved

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26
Q

Summarise the aetiology of erythema multiforme

A

Precipitating factor only found 50% of the time

Usually due to a preceding infection
Most commonly HERPES SIMPLEX VIRUS and MYCOPLASMA PNEUMONIAE
Can also be due to:
HIV
EBV
CMV
Hep B
Herpes zoster
Sulphonamides
Penicillins
Anticonvulsants

Other precipitating factors:
Inflammatory - e.g. rheumatoid arthritis, SLE, sarcoidosis, ulcerative colitis
Malignancy - e.g. lymphomas, leukaemia, myeloma
Radiotherapy

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27
Q

Summarise the epidemiology of erythema multiforme

A
Can occur in any age group
More common in males
Peak incidence in 20s and 30s
20% of cases occur in children
Children often have more severe form
Recurrent in 30% of patients
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28
Q

What are the presenting symptoms of erythema multiforme?

A

Prodrome - fever, aches

Rapid onset over 24-48 hours
Symmetrical
Target lesions - central necrosis surrounded by erythematous rings
Tender, itchy, burning rash
Lesions start on hands and spread

Lesions may fade and leave pigmentation

Erythema multiforme major:
Painful, itchy, crusting, bleeding ulcerations on mouth

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29
Q

What are the signs on physical examination of erythema multiforme?

A

Classic target (bull’s eye) lesions with a rim of erythema surrounding a paler area
Vesicles/bullae
Urticarial plaques
Lesions are often symmetrical and distributed over the arms and legs including the palms, soles and extensor surfaces

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30
Q

What are the appropriate investigations for erythema multiforme?

A

Mainly a clinical diagnosis

FBC - elevated WCC
ESR/CRP - elevated
U&Es - may show elevated BUN, creatinine if dehydrated due to decreased fluid intake (painful ulcers involving mouth make this harder)
HSV serology
Cold-haemagglutination serology - positive if mycoplasma
Mycoplasma pneumoniae titre

Imaging – exclude sarcoidosis and atypical pneumonia
Skin biopsy – histology and direct immunofluorescence if in doubt about diagnosis

31
Q

Define molluscum contagiosum

A

Cutaneous disorder caused by pox virus resulting in pink, pearly, smooth papules with central umbilication, affecting children and immunocompromised adults mainly by direct skin to skin contact

32
Q

Summarise the aetiology of molluscum contagiosum

A

Caused by molluscum contagiosum virus, a type of pox virus
MCV 1 and 1v are seen in children as the result of child-to-child contact or fomites
MCV 2 is a sexually transmitted virus noted in the groin in adults or generalised in immunocompromised adults
MCV 3 is a rare subtype in any age group

33
Q

Summarise the epidemiology of molluscum contagiosum

A

Most commonly children - affects 5-12% of children
90% of patients are under 15 years old
More common in tropical climates

34
Q

What are the presenting symptoms of molluscum contagiosum?

A

Incubation period: 2-8 weeks
Usually ASYMPTOMATIC papules
Pearly, flesh coloured papules which form dome
There may be tenderness, pruritus and eczema around the lesion in 1/3rd of patients
Lesions last for around 8 months

35
Q

What are the signs on physical examination of molluscum contagiosum?

A

Firm, smooth, umbilicated papules
Usually 2-5 mm in diameter
In children: tends to occur on the trunk and the extremities
In adults: tends to occur on the lower abdomen, genital area and inner thighs (suggesting sexual contact)
Surrounding erythema, inflammation and swelling

36
Q

What are the appropriate investigations for molluscum contagiosum?

A

Mainly clinical diagnosis
Curretage biopsy - shows Henderson-Patterson bodies
Dermatoscopy

37
Q

Define cellulitis and erysipelas

A

A spreading acute bacterial skin infection usually caused by streptococcus pyogenes or staphylococcus aureus.

Cellulitis is a deep infection of the dermis and subcutaneous tissue.

Erysipelas is a superficial infection of the epidermis and superficial lymphatics.

38
Q

Summarise the aetiology and risk factors of cellulitis and erysipelas

A

Most common beta haemolytic group A streptococcus pyogenes or staphylococcus aureus

Risk factors:
Open wound - trauma, bite, wound, ulcer, cannula
Immunosuppression - diabetes, HIV, alcohol use

39
Q

Summarise the epidemiology of cellulitis and erysipelas

A

Common condition

More common in extremes of age or immunocompromised

40
Q

What are the presenting symptoms of cellulitis and erysipelas?

A
Lesion:
Red
Painful
Oedematous/swollen
Warm
Acute onset

Erysipelas - raised, well demarcated, prodrome of fever, malaise

41
Q

What are the signs on physical examination of cellulitis and erysipelas?

A

Erythematous, oedematous, tender rash on extremities or face
Cellulitis - poorly demarcated
Erysipelas - well demarcated, raised

42
Q

What are the appropriate investigations for cellulitis and erysipelas?

A

FBC - increased WBC
ESR/CRP - elevated
Blood culture
Wound swab and culture - MC&S

43
Q

What is the appropriate management of cellulitis and erysipelas?

A
Conservative:
Analgesia
Bed rest
Elevation
Draw around it to monitor spread or shrinkage
Fluids
Sterile dressings

Medical:
Antibiotics - oral flucloxacillin (IV if severe)
Vancomycin if MRSA

44
Q

What are the possible complications of cellulitis and erysipelas?

A

Sepsis
Necrotising fasciitis
Abscess
Local necrosis

45
Q

Summarise the prognosis of cellulitis and erysipelas

A

The prognosis of cellulitis is excellent.
Most episodes of cellulitis resolve with therapy, and major sequelae are absent
May leave residual damage to draining lymphatics and perhaps increase the likelihood of recurrence in the future

46
Q

Define pressure sores

A

Localised injury to the skin and/or underlying tissue usually over a bony prominence, as a result of pressure or of pressure in combination with shear.

47
Q

Summarise the aetiology and risk factors of pressure sores

A

Constant pressure limits blood flow to the skin leading to tissue damage
They occur as a result of pressure, friction and shear

Risk factors:
Elderly
Immobile
Impaired sensation
Diabetes
48
Q

Summarise the epidemiology of pressure sores

A

Very common in hospitals

Occurs more commonly in elderly

49
Q

What are the presenting symptoms and signs on physical examination of pressure sores?

A

Occurs mostly over bony prominences or body parts eg sacrum and heel
subjected to sustained localised pressure
Shallow open wound or tissue loss on areas of pressure
Tenderness and warmth around area
They may become infected leading to fevers, erythema and foul smell

50
Q

What are the appropriate investigations for pressure sores?

A

NO investigations necessary - Clinical diagnosis

Waterlow Score is used to predict risk of pressure sores in patients

51
Q

Define varicella-zoster

A

Infection with varicella-zoster virus (a type of herpesvirus HSV3) which causes chickenpox in the acute infection, remains dormant in the dorsal root ganglion and can reactivate in times of stress and shingles

52
Q

Summarise the aetiology of varicella-zoster

A

Caused by infection with HSV3 varicella-zoster virus
Spread by respiratory droplets and direct lesion contact
Primary infection causes chickenpox
VZV can remain dormant in the dorsal root or trigeminal ganglia for many years
When stressed, immunocompromised, increased age can reactivate to cause shingles

Chickenpox is contagious from 48 hours before until all vesicles have crusted

53
Q

Summarise the aetiology of varicella-zoster

A

Chickenpox - more common in children, peak 4-10 years old

Varicella peak >50 years old

54
Q

What are the presenting symptoms and signs on physical examination of varicella zoster?

A

Chickenpox:
Fever, headache, weakness
Flat, red, itchy spots on trunk, scalp and face which become elevated and then develop into fluid-filled vesicles
Crust over in 1-2 days

Shingles:
Pain, itching tingling in dermatomal lesion
Unilateral painful vesicular rash in dermatomal distribution

55
Q

What are the appropriate investigations for varicella zoster?

A
Mainly clinical diagnosis
Swab of lesion:
PCR - VZV DNA
Viral culture - positive VZV
Blood test for varicella antibodies

Histology of vesicle fluid - multinucleated giant cells

56
Q

What is the management of varicella zoster?

A

Chickenpox:
Supportive - analgesia, antihistamine, calamine lotion for anti-pruritic properties
Adults with chickenpox - oral acyclovir, valaciclovir or famciclovir if immunocompetent, IV if immunocompromised

Shingles:
Oral acyclovir

57
Q

What are the possible complications of varicella zoster?

A
Chickenpox:
Skin infection
Scarring
Pneumonia
Hepatitis
Encephalopathy
Meningitis

Shingles:
Postherpetic neuralgia
Herpes zoster ophthalmicus - can lead to blindness
Superinfection of skin lesions
Ramsay-Hunt syndrome - ear pain, hearing loss, tinnitus, facial weakness

58
Q

Summarise the prognosis of varicella zoster

A

Chickenpox is a self-limiting illness

59
Q

Define candidiasis

A
Candidal/yeast infection of the skin, most commonly caused by candida albicans
Infections include:
Oral candidiasis (oral thrush)
Angular cheilitis
Vulvovaginal candidiasis (genital infection in women)
Balanitis (penile infection)
Intertrigo (skin fold infections)
Napkin dermatitis (nappy or diaper rash)
Chronic paronychia (nail fold infection)
Onychomycosis (nail plate infection)
Chronic mucocutaneous candidiasis
60
Q

Summarise the aetiology of candidiasis

A

Most common causative agent is candida albicans
Often opportunistic infection in those who are immunocompromised when invasive candidiasis

Risk factors:
Diabetes mellitus
Antibiotics - causes destruction of other bacteria allowing candida overgrowth
Inhaled corticosteroids
Immunosuppresion - HIV, long-term corticosteroids, chemotherapy, radiotherapy
Extremes of age
High oestrogen - contraceptive pill, pregnancy
Warm climate
Underlying skin condition

61
Q

Summarise the epidemiology of candidiasis

A

40-70% of health children and adults

62
Q

What are the presenting symptoms and signs on physical examination of candidiasis?

A

White, fluffy, cottage cheese-looking plaques in mouth, buccal cavity etc
Can be scraped off which may cause pain and shows underlying red, inflamed mucosa which may bleed

Vulvovaginitis - dysuria, thick white discharge, itching

Oseophageal candidiasis - dysphagia, odynophagia, white plagues in oesophagus

Erythema, Maceration, Satellite pustules, soreness and pruritus

63
Q

What are the appropriate investigations for candidiasis?

A

Tissue swab - microscopy and culture
Blood culture
Candida PCR
Candida antigen testing

64
Q

Define epidermoid and pillar cysts

A

An epithelial-lined, keratinous, debris-filled cyst often caused by a blocked hair follicle

65
Q

Summarise the aetiology of epidermoid and pillar cysts

A

Occlusion of the pilosebaceous gland
Can be caused by traumatic insertion of epidermal elements into the dermis
Embryonic remnants

Epidermoid cyst - lined by epidermis-like cells
Pillar cyst - lined by cells which look like those found in hair roots

66
Q

Summarise the epidemiology of epidermoid and pillar cysts

A

Very common at any age

67
Q

What are the presenting symptoms of epidermoid and pillar cysts?

A

Non-tender, slow-growing, round, firm skin swelling
There are often multiple
Common on hair-bearing regions of the body - face, scalp, trunk or scrotum
May become red, hot and tender if there is superimposed infection or inflammation

68
Q

What are the signs on physical examination of epidermoid and pillar cysts?

A

Firm, round, tethered lump under the skin
Overlying skin punctum
May discharge granular creamy material that smells bad

69
Q

What are the appropriate investigations of epidermoid and pillar cysts?

A

None

Skin biopsy or FNA if needed to rule out other diagnosis

70
Q

Define urticaria

A

A red, erythematous, raised, blanching, oedematous rash, likely due to histamine from mast-cell degranulation

Acute - lasts <6 weeks - often due to hypersensitivity allergic reaction
Chronic - >6 weeks

71
Q

Summarise the aetiology of urticaria

A

Mast cell degranulation and activation leading to release of histamine
Causes capillary leakage, which causes swelling of the skin and vasodilation - erythematous appearance

ACUTE urticaria:
Idiopathic
Allergies (foods, insect bites, stings, drugs)
Viral or parasitic infections
Skin contact with chemicals
Hereditary causes (in some cases of angioedema)
Physical stimuli - scraping skin, very hot or cold temperatures

CHRONIC urticaria:
Chronic spontaneous urticaria - medication, stress, infections
Autoimmune
Idiopathic

72
Q

Summarise the epidemiology of urticaria

A

Lifetime prevalence for acute urticaria - 20%
Acute urticaria more common in children and adolescents
Chronic urticaria mainly affects adults and more often women
Acute urticaria more common than chronic

73
Q

What are the presenting symptoms and the signs on physical examination of urticaria?

A

Red, erythematous, oedematous, blanching, raised lesions on the skin
Well-demarcated
Wheals - itchy with central white papule

40% associated with angioedema - swelling of soft-tissue of eyes, face, tongue, lips

Urticaria: swelling involving the superficial dermis, raising the epidermis (itchy wheels)
Angioedema: deeper swelling involving the dermis and subcutaneous tissues (tongue, lips)
Anaphylaxis: bronchospasm, facial and laryngeal oedema, hypotension

Acute - symptoms develop quickly but normally resolve within 48 hours
Chronic - rash persists for > 6 weeks

74
Q

What are the appropriate investigations of urticaria?

A

Clinical diagnosis in acute
May later use patch testing to determine cause

Chronic requires further investigations to determine cause:
FBC, ESR/CRP, IgE receptor antibody positive in chronic autoimmune urticaria