Skin Signs Of Systemic Disease Flashcards

1
Q

What is a leg ulcer

A

Open lesion between the knee and ankle joint that remains unhealed for at least 4 weeks

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2
Q

What is the most common cause of leg ulceration

A

Venous blood stasis

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3
Q

What causes arterial ulcers

A

Insufficient blood supply due to peripheral vascular disease

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4
Q

What causes venous ulceration

A

Increased hydrostatic pressure in the vessels

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5
Q

Where do the majority of venous ulcers occur

A

The gaiter area

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6
Q

Describe venous ulcers

A

Shallow exudative and warm

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7
Q

Give some signs of venous insufficiency

A

Ankle swelling
Varicose veins
Haemosiderin deposition
Venous eczema
Lipodermatosclerosis

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8
Q

What is lipodermatosclerosis

A

Inflammation and fibrosis of the subcutaneous fat layer, usually in the lower legs

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9
Q

How does lipodermatosclerosis present

A

Woody texture, skin appears hardened and reddish-brown

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10
Q

Where do arterial ulcers tend to affect

A

The foot

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11
Q

Presentation of arterial ulcers

A

Punched-out appearance, cold, white and shiny skin

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12
Q

Clinical signs or PAD

A

Absent peripheral pulses, delayed capillary refill, intermittent claudication

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13
Q

Investigations for leg ulcers

A

ABPI for arterial
Bloods
Patch testing for treatments
Biopsy to check for malignancy

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14
Q

Management of arterial ulcers

A

Managed by reducing modifiable risk factors

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15
Q

Management of venous ulcers

A

Compression stockings + elevation
De-sloughing if necessary
Control pain

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16
Q

Complications of leg ulceration

A

Infection
Contact allergy to dressings and topicals
Malignant transformation

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17
Q

What is epidermolysis bullosa

A

A group of inherited disorders with blister formation in response to mechanical trauma

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18
Q

What are the 3 main types of epidermolysis bullosa

A

Simplex, Junctional and dystrophic

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19
Q

Investigations for epidermolysis bullosa

A

Skin biopsy

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20
Q

Management of epidermolysis bullosa

A

Mainly supportive

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21
Q

Clinical presentation of epidermolysis bullosa

A

Skin blisters and erosions

22
Q

What is neurofibromatosis type 1

A

A genetic condition that causes tumours along the nervous system

23
Q

Inheritance in neurofibromatosis type 1

A

Autosomal dominant

24
Q

What causes neurofibromatosis type 1

A

Mutations in the NF1 gene

25
Main clinical sign of neurofibromatosis type 1
Cafe au lait macules
26
Other clinical signs of neurofibromatosis type 1
Plexiform neuroma, axillary or inguinal freckling, 2 or more lisch nodules
27
What mediates a type 1 allergic reaction
IgE
28
Routes of exposure that cause a type 1 allergic reaction
Skin contact, inhalation, ingestion and injection
29
Sensitisation stage of a type 1 allergy
Production of IgE by B cells in response to an initial allergen exposure Residual antibodies mind to circulating mast cells by Fc receptors
30
Allergic stage of a type 1 allergy
On re-exposure, allergen will bind to IgE coated mast cells, causing degranulation of histamine etc.
31
Clinical presentation of type 1 allergy
Urticaria, angioedema, wheezing, anaphylaxis
32
What are other names for urticaria
Hives, wheals, nettle rash
33
What is urticaria
Very itchy lesions which appear with 1 hour of interaction with an allergen
34
What is angioedema
Localised swelling of subcutaneous tissue or mucous membranes
35
Is angioedema pitting or non-pitting
Non-pitting
36
What investigations confirms anaphylaxis
Serum mast cell tryptase level
37
Testing for a type 1 allergy
Specific IgE bloodwork Prick testing Challenge test
38
What is used to manage anaphylaxis
Adrenaline autotinjector
39
What can be used to help asthma in patients with allergies
Mast cell stabiliser
40
Name one mast cell stabiliser
Sodium cromoglycate
41
Long term management of a type 1 allergy
Avoidance Antihistamines as first line Corticosteroids as second line
42
3 step plan for an acute allergic reaction
Chrophenamine at first sign of reaction Prednisolone if no resolution Adrenaline IV if symptoms get worse: become blue or collapse
43
What is the inheritance in tuberous sclerosis
Autosomal dominant
44
How is tuberous sclerosis characterised
By a range of benign tumours in various organ systems
45
Earliest cutaneous signs of tuberous sclerosis
Ash leaf macules
46
What are ash leaf macules
Depigmented macules
47
Other clinical signs of tuberous sclerosis
Shargreen patches and enamel pitting
48
How may an infant present with tuberous sclerosis
Seizures
49
Tumours seen in tuberous sclerosis
Periungual fibromas Facial angiofibromas Hamartomas/angiomyolipomas Bone cysts
50
What are periungual fibromas
Benign tumours around the nail