Other inflammatory skin disease Flashcards

1
Q

What’s exanthem?

A

Exanthem is a widespread rash occurring on the outside of the body and usually occurring in children

Cause: toxins, drugs, or microorganisms, an autoimmune disease

Examples: varicella-zoster, Scarlet fever, measles, rubella etc..

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2
Q

What’s toxic epidermal necrolysis?

A

Toxic epidermal necrolysis (TEN)

  • a potentially life-threatening skin disorder
  • most commonly seen secondary to a drug reaction
  • the skin develops a scalded appearance over an extensive area
  • TEN is severe end of a spectrum of skin disorders which includes erythema multiforme and Stevens-Johnson syndrome
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3
Q

Features of Toxic Epidermal Necrolysis

A
  • systemically unwell e.g. pyrexia, tachycardic
  • positive Nikolsky’s sign: the epidermis separates with mild lateral pressure
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4
Q

Drugs known to induce TEN

A

Drugs known to induce TEN

  • phenytoin
  • sulphonamides
  • allopurinol
  • penicillins
  • carbamazepine
  • NSAIDs
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5
Q

Management of TEN

A
  • stop precipitating factor
  • supportive care, often in ICU
  • intravenous immunoglobulin used first-line
  • immunosuppressive agents (ciclosporin and cyclophosphamide)
  • plasmapheresis
  • analgesia

*opthalmological input may be needed - if eye involved

* burns unit may be required for specialised skin care

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6
Q

Spot diagnosis

A

Urticaria

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7
Q

Characteristics of urticaria

A

Urticaria is characterised by:

  • weals (hives)
  • angioedema

Weal (or wheal)→ a superficial skin-coloured or pale skin swelling, usually surrounded by erythema (redness). Usually very itchy, it may have a burning sensation.

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8
Q

Pathophysiology of urticaria

A
  • release of chemical mediators from tissue mast cells and circulating basophils
  • these chemical mediators include histamine, platelet-activating factor and cytokines
  • the mediators activate sensory nerves and cause dilation of blood vessels and leakage of fluid into surrounding tissues
  • Bradykinin release causes angioedema
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9
Q

Causes of urticaria

A

*Severe allergic urticaria may lead to anaphylactic shock (bronchospasm, collapse)

*A single episode or recurrent episodes of angioedema without urticaria can be due to an angiotensin-converting enzyme (ACE) inhibitor drug

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10
Q

Diagnosis of acute urticaria

A

Acute urticaria

  • short history of weals that last less than 24 hours, with or without angioedema
  • A thorough physical examination should be undertaken to look for underlying causes
  • skin prick tests and radioallergosorbent tests (RAST) or CAP fluoroimmunoassay may be requested if a drug or food allergy is suspected in acute urticaria
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11
Q

Weals vs fungal infection

A

WEALS: Oedamatous DERMAL in urticaria

Fungal: EPIDERMAL, scaly

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12
Q

Urticaria vs urticarial vasculitis

A
  • Urticaria: comes and goes quickly (lasts for 24-48 hours)
  • Urticarial vasculitis (looks like urticaria) but lasts for longer, has a bit of bruise; may affect any organ (as vasculitis) and requires biopsy
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13
Q

Classification of urticaria (timeframe)

A
  • Acute → less than 6 weeks
  • Chronic → more than 6 weeks (not associated with allergy)
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14
Q

Is urticaria associated with an allergy?

A

URTICARIA does not = allergy!

Urticaria may be a feature of anaphylaxis but not always

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15
Q

Management of urticaria

A

Non-sedating anti-histamine → x4 the usual dose cetirizine/loratadine

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16
Q

Describe the rash + diagnosis

A

Maculopapular rash (some flat some bumpy spots)

It’s characteristic of exanthem

*in children usually viral

*in adult e.g. drug reaction/ HIV seroconversion

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17
Q

Drugs known to (commonly) cause skin changes

A
  • sulphonamides
  • anticonvulsants
  • penicillins
  • allopurinol
  • NSAIDs

*it may be 1-2 weeks delay in between starting the drug and rash; even if the drug has been stopped

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18
Q

Describe + diagnose

A

Haemorrhagic crusting of the lips

Typical for Steven-Johnson syndrome

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19
Q

Features of Stevens-Johnson syndrome

A
  • prodrome of fever and respiratory symptoms
  • two or more mucosal sites
  • possible severe eye and oral involvement
  • non-specific or targetoid eruption
  • prolonged course
20
Q

What happens in SJS/TEN? (pathophysiologically)

A
  • Epidermal death → a bit like in burns
  • fluids, electrolytes, protein loss

*mortality is 35%

21
Q

What to do if we see cutaneous vasculitis?

A

As vasculitis may affect any other organ → check for other systems involvement (particularly kidney)

  • FBC
  • U&Es
  • BP
  • urinalysis
  • LFTs (as hepatitis can trigger)
  • anti-bodies (lupus, rheumatoid, connective tissue etc)
  • inflammatory markers (if only cutaneous disease these can be normal but if also systemic these will be raised)
22
Q

What’s that?

Causes, describe

A

Purpura (vasculitis eruption)

Causes: vasculitis, low platelets, meningitis, HSP etc.

Description: Shower of individual little spots, coalescence, non-bleaching

23
Q

Name these lesions (each picture)

What disease are these associated with?

A
24
Q

Name these lesions (each picture)

What disease are these associated with?

A
25
Q

Name these lesions (each picture)

What disease are these associated with?

A
26
Q

Spot diagnosis

A

Erythema Nodosum

  • tender lumps
  • inflammation of the fat
27
Q

Causes of Erythema Nodosum

A

NO - idiopathic

D - drugs: sulphonamides, amoxicillin

O - OCP

S - sarcoidosis

U - UC, Crohn’s, Behcet’s

M - microbiology - strep, TB, viral

28
Q

Causes of pyoderma gangrenosum

A
  • nose, legs but also other sides
  • Hx: pustule, a nodule that rapidly expands and ulcerates
  • often multifocal (separate bits that may join up)
  • very painful

Treatment: underlying cause, oral steroids

29
Q

Overview of dermatomyositis

A
  • an inflammatory disorder
  • symmetrical, proximal muscle weakness and characteristic skin lesions
  • may be idiopathic or associated with connective tissue disorders or underlying malignancy
  • screening for an underlying malignancy is usually performed following a diagnosis of dermatomyositis
  • polymyositis is a variant of the disease where skin manifestations are not prominent
30
Q

Skin features of dermatomyositis

A

Skin features

  • photosensitive
  • macular rash over back and shoulder
  • heliotrope rash in the periorbital region
  • Gottron’s papules - roughened red papules over extensor surfaces of fingers
  • ‘mechanic’s hands’: extremely dry and scaly hands with linear ‘cracks’ on the palmar and lateral aspects of the fingers
  • nail fold capillary dilatation
31
Q

Other features (than skin) of dermatomyositis

A
  • proximal muscle weakness +/- tenderness
  • Raynaud’s
  • respiratory muscle weakness
  • interstitial lung disease: e.g. Fibrosing alveolitis or organising pneumonia
  • dysphagia, dysphonia
32
Q

Ix of dermatomyositis

A
  • the majority of patients (around 80%) are ANA positive
  • around 30% of patients have antibodies to aminoacyl-tRNA synthetases (anti-synthetase antibodies), including:
    • antibodies against histidine-tRNA ligase (also called Jo-1)
    • antibodies to signal recognition particle (SRP)
    • anti-Mi-2 antibodies
33
Q

Spot diagnosis

A

Heliotrope rash → feature of dermatomyositis

34
Q

Spot diagnosis

A

Gottron’s papules → feature of dermatomyositis

35
Q

Management of dermatomyositis

A
  • Steroids
  • Check CK → if muscle involvement
  • Do other Ix → possible malignancy (another flashcard)
36
Q

Spot diagnosis

A

Erythema multiforme

  • target lesions (for true target lesions at least 3 colours in a single lesion)
  • viruses: herpes simplex virus (the most common cause), Orf*
  • idiopathic
  • bacteria: Mycoplasma, Streptococcus
  • drugs: penicillin, sulphonamides, carbamazepine, allopurinol, NSAIDs, oral contraceptive pill, nevirapine
  • connective tissue disease e.g. Systemic lupus erythematosus
  • sarcoidosis
  • malignancy
37
Q

Spot diagnosis

A

Inverse Flexural Psoriasis

  • scale is lost in moist flexural sites
  • fissure in the crease
  • usually in the natal cleft

Treatment: similar to psoriasis; mild- moderate topical steroids

(no vit D or tar as it will irritate delicate areas)

38
Q

Spot diagnosis

A

Tinea corporis

39
Q

Treatment for this

A

Do nothing - Seborrhagic keratoses

If not sure what’s that - refer to dermatology

  • well-demarcated
  • depressions on the surfaces
  • inclusion cysts (depigmentation)

Treat only if symptomatic: curettage, freeze

40
Q

Diagnosis?

(unwell patient)

A

Necrotising fascitis

41
Q

Diagnosis?

A

Superficial BCC

  • looks like a red scaly plaque with no characteristic features
  • biopsy it - to be sure

*this characteristic one - pearled age

* do not use cryotherapy for it

* imiquimod, incision, curettage used

42
Q

Treatment of acne in pregnancy

A
  • benzoyl peroxide - the only Rx to be used in pregnancy
  • the only other option - erythromycin
43
Q

Diagnosis?

A

It could be BCC or SCC

*rather SCC though due to keratin bits

44
Q

Treatment to it?

Clue: Pt can’t go to work

A

Eczema infected with impetigo (in this case impregnated contact dermatitis)

  • scaling
  • diffuse over palmar surfaces
  • golden crust

Treatment: oral antibiotics to cover strep and staph, potent topical steroid

Ix: swab, do a patch test (type IV delayed-type allergy)

45
Q

lady is well, no other symptoms

A

Rosacea

  • papules within redness

Treatment: oral tetracyclines, topical metronidazole

*but problem will be recurrent