6- Dermatology (Blistering and Pigment disorders) Flashcards

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1
Q

Blistering disorders
Split into

A
  • Immunobullous disease
  • Blistering skin infections
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2
Q

Immunobullous disease

A

o Bullous pemphigoids
o Pemphigus vulgaris

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3
Q

Blistering skin infections

A

o Herpes simplex
o Porphyria cutanea tarda

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4
Q

Bullous pemphigoid
Background

A
  • Autoimmune
  • Blistering, itchy skin disorder usually affect elderly
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5
Q

Bullous pemphigoid pathophysiology

A

Pathophysiology
- Autoantibodies against antigens between the epidermis and dermis causing a sub-epidermal split in the skin

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6
Q

Bullous pemphigoid presentation

A

It usually starts with an itchy, raised rash. As the condition develops, large blisters can form on the skin. It may last a few years and sometimes causes serious problems, but treatment can help manage the condition in most cases.

  • Tense, fluid-filled blisters on an erythematous base
  • Lesions are often itchy
  • Preceded by non-specific itchy rash
  • Does not affect mucosal areas
  • Trunk and limbs
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7
Q

management of bullous pemphigoid

A

General
- Wound dressings
- Monitor for infection

Topical for localised disease
- Topical steroid

Oral for widespread disease
* Oral steroids
* Tetracycline and nicotinamide
* Immunosuppressive agents
* Azathioprine
* Mycophenolate mofetil
* Methotrexate

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8
Q

Pemphigus vulgaris
Background

A
  • Autoimmune
  • Blistering skin disorder which usually affects middle-aged people
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9
Q

Pathophysiology Pemphigus vulgaris

A
  • Autoantibodies against antigens with the epidermis causing intra-epidermal split in the skin
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10
Q

presentation pemphigus vulgaris

A
  • Flaccid easily ruptured blisters forming erosions and crusts
  • Lesions are painful
  • Usually affects mucosal area
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11
Q

management of pemphigus vulgaris

A

General measures
- Wound dressings
- Monitor for infection
- Good oral care

Oral therapies
- High dose oral steroids
- Immunosuppressives e.g. methotrexate, azathioprine, cyclophosphamide, mycophenolate mofetil

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12
Q

Bullous pemphigois vs pemphigus vulgaris

A

Types of blisters

Pemphigus is characterized by shallow ulcers or fragile blisters that break open quickly. Pemphigoid presents with stronger or “tense” blisters that don’t open easily.

Location: Initial site also varies; pemphigus vulgaris generally starts in the oral mucosa whereas bullous pemphigoid affects the extremities at onset. From onset, pemphigus vulgaris will spread widely to the face, scalp, flexural surfaces, and trunk; bullous pemphigoid moves inward to the flexural surfaces and trunk.23

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13
Q

Pigment disorders

A
  • Hypopigmentation -reduced
  • Depigmentation- complete loss
  • Hyperpigmentation – increased

Common conditions
- Vitiligo
- Melasma

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14
Q

Vitiligo
Background

A
  • Acquired depigmenting disorder
  • Complete loss of pigment cells -> melanocytes
  • Presents at any age
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15
Q

Pathophysiology of vitiligo

A
  • Autoimmune disorder where innate immune system causes loss of melancoytes, leading to loss of pigment
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16
Q

presentation of vitiligo

A
  • Single patch or multiple patches of depigmentation
  • Often symmetrical
  • Common sites are exposed areas
    o Face
    o Hands
    o Feet

Others
o Genitalia
o Body fold
- Favours sites of injury e.g. Koebner phenomenon

17
Q

management of vitiligo

A

Management
- Minimise skin injury e.g. cut, graze, sunburn -> trigger for new patch
- Topical treatments
o Steroids
o Calcineurin inhibitors e.g. tacrolimus
- Phototherapy e.g. UVB therapy
- Oral immunosuppressants e.g. methotrexate, ciclosporin and mycophenolate mofetil

18
Q

Melasma

Background

A
  • Acquired chronic skin disorder
  • Increased pigmentation in the skin -> hyperpigmentation
19
Q

melasma risk factors and causes

A
  • Genetic predisposition
  • Triggers
    o Sun exposure
    o Hormonal changes e.g. pregnancy and contraceptives
20
Q

Pathophysiology of melasma

A
  • Overproduction of melanin by melanocytes
21
Q

Presentation of melasma

A
  • Brown macule (freckle-like spots) or larger patches with an irregular border
  • Symmetrical distribution
  • Common sites
    o Forehead
    o Cutaneous upper lips
    o Cheeks
  • Others
    o Neck
    o Shoulders
    o Upper arms