Dermatology - Skin & Systemic Disease Flashcards

1
Q

What is acanthosis nigricans?

A

Skin disorder characterised by hyperpigmentation** (darkening) and **hyperkeratosis (thickening) of the skin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What underlying malignant systemic disease can acanthosis nigricans indicate?

A

GI malignancy → especially stomach

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Acanthosis nigricans can be a sign of a benign underlying condition. What is the most common?

A

Obesity related - associated with insulin resistance (e.g. T2DM)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Give some other benign causes of acanthosis nigricans

A
  • Can be syndromic → Cushing’s disease, PCOS
  • Can be drug induced (e.g. insulin use, nicotinic acid, systemic steroids, hormone treatments)
  • Can be hereditary (autosomal dominant)
  • Can occur in healthy individuals, mainly African-American – most commonly velvety lesions over hands and feet
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Location of acanthosis nigricans?

A

Skin folds (axilla, groin, back of neck)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Presentation of acanthosis nigricans?

A
  • Often velvety texture
  • Can be papillomatoses (finger-like growths) and skin tags occur in surrounding skin
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is necrobiosis lipoidica?

A

A rare granulomatous skin disorder.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What systemic disease can necrobiosis lipoidica indicate?

A

Diabetes (insulin dependent)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Presentation of necrobiosis lipoidica?

A
  • One or more tender yellow/brown patches on lower legs for several months – years
  • Centre of patch is shiny, pale, thin with telangiectasia (visible blood vessels)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Management of necrobiosis lipoidica?

A

Doesn’t always require treatment but can use:

  • Topical steroids
  • Oral ciclosporin
  • Phototherapy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is granuloma annulare?

A

A common inflammatory skin condition typified clinically by annular, smooth, discoloured papules** and **plaques**, and **necrobiotic granulomas on histology.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Who is granuloma annulare most common in?

A

Most common in children, teenagers and young adults.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Pathophysiology of granuloma annulare?

A

Hypersensitivity reaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What systemic disease can granuloma annulare indicate?

A

Sometimes associated with diabetes** and **hyperlipidaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Describe the plaques in granuloma annulare

A

Smooth, discoloured, thickened, annular (round)

  • Affected areas only tender when knocked
  • Plaques tend to change appearance slowly
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Management of granuloma annulare?

A
  • Most often require no treatment as plaques disappear in several months without a scar
  • Can remain for years
  • Treatments include:
    • Steroids or imiquimod
    • Calcineurin inhibitors (tacrolimus)
    • Widespread → systemic immunosuppressants or phototherapy
17
Q

What is erythema nodosum?

A

An inflammatory disorder affected subcutaneous fat.

18
Q

Pathophysiology of erythema nodosum?

A

Hypersensitivity response (often due to recent infection in otherwise healthy individuals).

19
Q

What systemic disease can erythema nodosum indicate?

A

Infection, drugs and inflammatory diseases

20
Q

Who is erythema nodosum more common in?

A

Age 20-45 y/o.

More common in women.

21
Q

Give some diseases that can trigger erythema nodosum

A
  • Group A strep
  • primary TB
  • pregnancy
  • malignancy
  • IBD
  • chlamydia
  • leprosy
22
Q

Give some drugs that can trigger erythema nodosum

A

NSAIDs, amoxicillin, COP, sulfonamides

23
Q

Presentation of lesions of erythema nodosum?

A
  • Presents as tender red nodules on anterior shins (sometimes thighs and forearms).
  • Appear for 1-2 weeks which appear like bruises as they resolve
24
Q

Management of erythema nodosum?

A
  • Treat underlying infection
  • Bed rest, supportive bandages & anti-inflammatories
  • Normally subsides in 3-6 weeks
25
Q

What is pyoderma gangrenosum?

A

Auto-inflammatory disease – excessive immune response due to a neutrophil dysfunction (neutrophilic dermatosis) that presents as a rapidly enlarging, very painful ulcer.

26
Q

What age group does pyoderma gangrenosum typically affect?

A

>50 y/o

27
Q

What underlying disease can pyoderma gangrenosum be associated with?

A

Thought to be a reaction to a disease e.g.:

  • IBD
  • Rheumatoid arthritis
  • Myeloid blood disorders (leukaemia)
  • PAPA syndrome

BUT 50% of those affected don’t have these risk factors.

28
Q

Describe the lesion in pyoderma gangrenosum

A
  • Fast growing, highly painful ulcer
  • Purple, undermined borders
  • May be multiple ulcers (not gangrenous)
29
Q

Management of pyoderma gangrenosum?

A
  • Remove necrotic tissue and provide expert wound care
  • Avoid surgical debridement when ulcers are active as may lead to increased ulcer size
  • Abx not useful UNLESS 2ary infection
  • Steroids → given topically or systemically depending on size/spread