Miscellaneous Flashcards

1
Q

What is acanthosis nigricans?

A

Symmetrical, brown, velvety plaques, often found on the neck, axilla and groin.

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2
Q

What conditions is acanthosis nigricans associated with?

A
T2DM
GI cancer
Obesity
PCOS
Acromegaly
Cushing's disease
Hypothyroidism
Familial
Prader-Willi syndrome
COCP and nicotinic acid
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3
Q

What is the pathophysiology of acanthosis nigricans?

A

Increased insulin resistance –>
Hyperinsulinemia –> Stimulation of keratinocytes and dermal fibroblasts –> Proliferation via interation with insulin-like growth factor-1.

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4
Q

What is acne rosacea?

A

Chronic skin disease of unknown aetilogy.

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5
Q

What is the appearance of acne rosacea?

A

Typically affects the nose, cheeks and forehead
Flushing - first symtpom
Telangiectasia
Develops into persistent erythema with papules and pustules
Rhinophyma
Ocular involvement - blepharitis

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6
Q

What may exacerbate the symptoms of ace rosacea?

A

Sunlight

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7
Q

What is the treatment of acne rosacea?

A
Topical metronidazole
Topical brimonidine
Systemic abx: Oxytetracycline
Daily suncream
Comflage cream
Laser therapy
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8
Q

What is actinic (solar) keratoses?

A

A common pre-malignant skin lesion that develops as a consequence of chronic sun exposure.

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9
Q

How does actinic keratoses appear?

A

Small, crusty or scaly lesions
Pink, red, brown or skin colour
Typically on sun-exposed areas
Multiple lesions may be present

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10
Q

What is the management of actinic keratoses?

A
Sun avoidance, sun cream
Fluorouracil cream
Topical diclofenac
Topical imiquimod
Cryotherapy
Curettage and cautery
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11
Q

What is Bowen’s disease?

A

A type of intraepidermal squamous cell carcinoma.

More common in elderly females - 3% development into invasive cancer.

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12
Q

How does Bowen’s disease present?

A

Red, scaly patches

Often occur on sun-exposed areas

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13
Q

What are the management options of Bowen’s disease?

A

Topical 5-fluorouracil or imiquimod
Cryotherapy
Excision

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14
Q

What is a cherry haemangioma?

A

(Campbell de Moran spots)

Benign skin lesions which contain an abnormal proliferation of capillaries.

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15
Q

What are the features of a cherry haemangioma?

A

Erythmatous, papular lesion
Typically 1-3 mm in size
Non-blanching
Not found on the mucous membranes

Benign - no treatment required

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16
Q

What is chondrodermatitis nodularis helicis (CNH)?

A

Common and benign - development of a painful nodule on the ear.

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17
Q

What are the causes of chondrodermatitis nodularis helicis (CNH)?

A

Persistent pressure on ear
Trauma
Cold

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18
Q

What is the management of chondrodermatitis nodularis helicis (CNH)?

A
Reducing pressure on the ear: foam 'ear protectors' may be used during sleep
Cryotherapy
Steroid injections
Collage injections
Surgery
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19
Q

What is dermatitis herpetiformis?

A

An autoimmune blistering skin disorder associated with coeliac disease. Caused by IgA deposition in the dermis.

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20
Q

What is the presentation of dermatitis herpetiformis?

A

Itchy, vesicular skin lesions on the extensor surfaces (e.g. elbows, knees, buttocks)

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21
Q

How is dermatitis herpetiformis diagnosed?

A

Skin biopsy: direct immunofluorescence shows deposition of IgA in a granular pattern in the upper dermis

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22
Q

How is dermatitis herpetiformis managed?

A

Gluten-free diet

Dapsone

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23
Q

What is eczema herpeticum?

A

A severe primary infection of the skin by HSV 1 or 2.

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24
Q

Who does eczema herpeticum usually present in?

A

More commonly seen in children with atopic eczeema and often presents as a rapidly progressing painful rash.

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25
How does eczema herpeticum usually present?
Monomorphic punched-out erosions (circular, depressed, ulcerated lesions), usually 1-3mm in diameter.
26
What is the treatment f eczema herpeticum?
Potentially life-threatening, children should be admitted for IV aciclovir.
27
What is erythema ad igne?
Caused by over exposure to infrared radiation. Reticulated, erythmatous patches with hyperpigmentation and telangiectasia. (Typical history elderly woman who always sits next to an open fire) (Looks like mottled skin)
28
What is erythema ad igne a risk factor of?
Squamous cell skin cancer
29
What is erythema nodosum?
Inflammation of subcutaneous fat Typically causes tender, erythmatous, nodular lesions Typically occurs over the shins, may occur elsewhere Usually resolves within 6 weeks Lesions heal without scarring
30
What are the causes of erythema nodosum?
Infection - streptococci, TB, brucellosis Systemic disease - sarcoidosis, IBD, Behcet's Malignancy/lymphoma Drugs - penicillins, sulphonamides, COCP Pregnancy
31
What is erythrasma?
Generally asymptomatic, flat, slightly scaly, pink or brown rash usually found in the groin or axillae.
32
What causes erythrasma?
Overgrowth of the diphtheroid Coryneacterium minutissimum
33
How is erythrasma diagnosed?
Wood's light reveals a coral-red fluorescence
34
What is the treatment of erythrasma?
Topical miconazole or antibacterial are usually effective. | Oral erythromycin.
35
What is erythroderma?
A term used when more than 95% of the skin is involved in a rash of any kind. Extensive exfoliation may also occur.
36
What are the causes of erythroderma?
``` Eczema Psoriasis Drugs e.g. gold Lymphomas, leukaemias Idiopathic ```
37
What is erythrodermic psoriasis?
May result from progression of chronic disease to an exfoliative phase with plaques covering most of the body. Associated with mild systemic upset. May be triggered by withdrawal of systemic steroids.
38
What is granuloma annulare?
Quite large papular lesions that are often slightly hyperpigmented and depressed centrally Typically occur on the dorsal surfaces of the hands and feel and extensor aspects of arms and legs.
39
What are some associations of granuloma annulare?
Diabetes mellitus
40
What is hereditary haemorrhagic telangiectasia (HHT)?
(Osler-Weber-Rendu syndrome)
41
What is the inheritance pattern of HHT?
Autosomal dominant condition | 50% occur without fHx
42
What is the presentation of HHT?
Multiple telangiectasia over the skin and mucous membranes.
43
What are the diagnostic criteria for HHT?
Epistaxis Telangiectases Visceral lesions e.g. GI telangiectasia, pulmonary AVM, hepatic AVM, cerebral AVM, spinal AVM. Family history: 1st degree relative 2/4 - possible 3/4 - definitive diagnosis
44
What is hirsuitism?
Describes androgen-dependent hair growth in women
45
What is hypertrichosis?
Describes androgen-independent hair growth in women.
46
What are the causes of hirsuitism?
``` PCOS (most common) Cushing's syndrome CAH Androgen therapy Obesity: due to insulin resistance Adrenal tumour Androgen secreting ovarian tumour Drugs: phenytoin, corticosteroids. ```
47
What scoring system is used to assess hirsutism?
Ferriman-Gallwey score: | >15 moderate - severe
48
What is the management of hirsuitism?
Weight loss Cosmetic techniques COCP (Dianette) Topical eflornithine
49
What are causes of hypertrichosis?
Drugs: minoxidil, ciclosporin, diazoxide Congenital Porphyria cutanea tarda Anorexia nervosa
50
What is hyperhidrosis?
Excessive production of sweat
51
What are the management options of hyperhidrosis?
Topical aluminium chloride Iontophoresis Botulinum toxin Surgery
52
What are keloid scars?
Tumour-like lesions that arise from the connective tissue of a scan and extend beyond the dimensions of the original wound.
53
What are predisposing factors to developing a keloid scar?
Ethnicity: darker skin Younger adults Common sites: sternum, shoulder, neck, face, extensor surface of limbs, trunk.
54
What is the treatment of keloid scars?
Intra-lesional steroids e.g. triamcinolone | Excision
55
What formulation of ketoconazole be used?
Only topical due to risk of heptic toxicity systemically
56
What is koebner phenomenon?
Typically in psoriasis, describes the formation of psoriatic skin lesions on parts of the body that aren't typically where a person with psoriasis experiences lesions, following an injury.
57
What conditions is Koebner phenomenon associated with?
``` Psoriasis Vitiligo Warts Lichen planus Lichen sclerosus Molluscum contagiosum ```
58
What is Lentigo maligna?
A type of melanoma in-situ. Typically progresses slowly but may at some stage become invasive causing lentigo meligna melanoma.
59
What is Leukoplakia?
Premalignant condition which presents as white, hard spots on the mucous membranes of the mouth, More common in smokers.
60
What are the differentials for Leukoplakia?
Candidiasis | Lichen planus
61
How is the diagnosis for Leukoplakia made?
Biopsies
62
What is lichen planus?
A skin disorder of unknown aetiology, most probably immune-mediated
63
What are the features of lichen planus?
Itchy, papular rash most common on the palms, soles, genitalia and flexor surfaces of the arms. Often polygonal in shape, with 'white-lines' pattern on the surface (Wickham's striae) Koebner pnenomenon may be seen Oral involvement (50%) Nails - thinning of nail plate, ridging.
64
What drugs can cause lichen planus eruptions?
Gold Quinine Thiazides
65
What is the management of Lichen Planus?
Potent topical steroids Benzydamine mouthwash Extensive - oral steroids or immunosuppression.
66
What is Lichen sclerosus?
Inflammatory condition usually affecting the genitalia and more common in elder females. Leads to atrophy of the epidermis and white plaques forming.
67
What are the features of lichen sclerosus?
Itch | White lesions, typically on genitalia.
68
How is lichen sclerosus diagnosed?
Clinical grounds | Biopsy can be performed
69
What is the management of lichen sclerosus?
Topical steroids and emollients
70
What is a potential complication of lichen sclerosus?
Increased risk of vulval cancer
71
What is the differential diangosis for lichen sclerosus?
VIN or cancer
72
What are indications for a biopsy in lichen sclerosus?
``` Unsure diagnosis Suspicion of neoplastic change Poor response to treatment Extragenital LS Pigmented areas ```
73
What is a lipoma?
A common, benign tumour of adipocytes.
74
What is the pathophysiology of a lipoma?
Generally found in subcutaneous tissues | May occur in deeper tissues, malignant transformation to liposarcoma is rare.
75
What are the features of a lipoma?
Smooth, mobile, painless lump.
76
What is the management of a lipoma?
May be observed, if diagnosis uncertain or compressing on surrounding structures then may be removed.
77
What are the features of a liposarcoma?
``` Features suggestive or sarcomatous change: Size > 5cm Increasing size Pain Deep anatomical location ```
78
What are Milia?
Milia are small, benign, keratin-filled cysts that typically appear around the face. They may appear at any age but they are more common in newborns.
79
What is mycosis fungoides?
A rare form of T-cell lymphoma affecting the skin
80
What are the features of mycosis fungiodes?
Itchy, red patches | Lesions tend to be of different colours in contrast to eczema/psoriasis where there is greater homogenicity
81
What is nickel dermatitis?
A common cause of allergic contact dermatitis, type 4 hypersensitivity reaction.
82
How is nickel dermatitis diagnosed?
Skin patch test
83
What is Pellagra?
A disease caused by nicotinic acid deficiency
84
What are the features of pellagra?
Dermatitis (brown scaly rash) Diarrhoea Dementia, depression Death if not treated
85
What are the causes of pellagra?
Isoniazid therapy | More common in alcoholics
86
What is Polymorphic eruption of pregnancy?
A pruritic condition associted with last trimester Lesions in abdominal striae Periumbilical area often spared
87
What is the management of polymorphic eruption of pregnancy?
Emollients | Mild potency topical steroids and oral steroids
88
What is porphyria cutanea tarda?
Most common hepatic porphyria. Due to an inherited defect in uroporphyrinogen decarboxylase or caused by hepatocyte damage e.g. alcohol, hepatitis C, oestrogen.
89
What are the features of Porphyria cutanea tarda?
Photosensitive rash with blistering and skin fragility on the face and dorsal aspect of hands. Hypertrichosis (excessive hair growth) Hyperpigmentation
90
What are the investigations of porphyria cutanea tarda?
Urine: elevated uroporphyrinogen and pink fluorescence of urine under Wood's lamp Serum iron ferritin level is used to guide therapy
91
What is the management of porphyria cutanea tarda?
Chloroquine | Venesetion - preferred if iron ferritin is above 600 ng/ml
92
What is a port wine stain?
Vascular birthmarks, tend to be unilateral. | Deep red or purple in colour
93
What is the prognosis of port wine stain?
Do not spontaneously resolve, often darken and become raised over time.
94
What is the treatment of port wine stains?
Cosmetic camouflage | Laser therapy
95
What are the causes of pruritis?
``` Liver disease Iron deficiency anaemia Polycythaemia Chronic kidney disease Lymphoma Hyper/Hypothyroidism Diabetes Pregnancy 'Senile' pruritis Urticaria Skin disorders: eczema, scabies, psoriasis, pityriasis rosea ```
96
When pruritis is caused by liver disease, what other features may be present?
History of alcohol excess Stigmata of chronic liver disease: spider naevi, bruising, palmar erythema, gynaecomastic. Evidence of decompensation ascites, jaundice, encephalopathy.
97
When pruritis is caused by iron deficiency anaemia, what other features may be present?
Pallor | Other signs: kolionychia, atrophic glossitis, post-cricoid webs, angular stomatitis.
98
When pruritis is caused by polycythaemia, what other features may be present?
Pruritis - 'after warm bath' Ruddy complexion Gout Peptic ulcer disease
99
When pruritis is caused by chronic kidney disease, what other features may be present?
Lethargy & pallor Oedema & weight gain Hypertension
100
When pruritis is caused by lymphoma, what other features may be present?
Night sweats Lymphadenopathy Splenimegaly, hepatomegaly Fatigue
101
What is pyoderma gangrenosum?
A rare condition causing large, painful sores (ulcers) to develop on the skin.
102
What are the features of pyoderma gangrenosum?
Typically on the lower limbs Initially small red papule Later deep, red, necrotic ulcer with a violeceous border Systemic symptoms: fever, myalgia
103
What are the causes of pyoderma gangrenosum?
``` Idiopathic - 50% IBD: UC or Crohn's RA, SLE Myeloproliferative disorders Lymphoma, myeloid leukaemias Monoclonal gammopathy (IgA) Primary biliary cirrhosis ```
104
What is the management of pyoderma gangrenosum?
Oral steroids | Other immunosuppresive therapy e.g. ciclosporin and infliximab.
105
What is a pyogenic granuloma?
Relatively common benign skin lesion. | Eruptive haemangioma
106
What are the causes of pyogenic granuloma?
Unknown | Linked with trauma, pregnancy, common in young women
107
What are the features of pyogenic granuloma?
Most common on the head/neck, upper trunk and hands. Initially small red/brown spot, rapidly progresses to form raised, red/brown lesions which are spherical in shape Lesions may bleed profusely or ulcerate
108
What is the management of a pyogenic granuloma?
Those associated with pregnancy may spontaneously resolve | Others may persist, removal may include curettage, cauterisation, cryotherapy and excision.
109
Give and example of a retinoid and what it can be used in the treatment of?
Isotretinoin Used in the treatment of severe acne. 2/3 of patients have long-term remission or cure following a course.
110
What are some of the adverse effects of isotretinoin?
``` Teratogenicity: 2 x forms of contraception Dry skin, eyes and lips/mouth Low mood Raised triglycerides Hair thinning Nose bleeds Intracranial hypertension c.i. tetracyclines Photosensitivity ```
111
What are salmon patches?
Salmon patches are a kind of vascular birthmark which can be seen in around half of newborn babies, they are pink and blotchy and found on the forehead, eyelids and nape. Usually fade over time.
112
What is a sebaceous cyst?
Encompasses epidermoid and pilar cysts. Due to proliferation of epidermal cells within the dermis. Contain a punctum. Excision of the cyst wall is necesssary to prevent recurrence.
113
What is seborrhoeic keratoses?
Benign epidermal skin lesions seen in older people
114
What are the features of seborrhoeic keratoses?
Large variation in colour from flesh to light-brown to black Stuck-on appearance Keratotic plugs may be seen on the surface
115
What is the management of seborrhoeic keratoses?
Reassurance that benign | Removal - curettage, cryosurgery, shave biopsy.
116
What are the differentials for Shin lesions?
Erythema nodosum Pretibial myxoedema Pyoderma gangrenosum Necrobiosis lipoidica diabeticorum
117
What is erythema nodosum?
Swollen fat under the skin, causing red bumps and patches. Symmetrical, erythematous, tender, nodules which head without scarring. (Often on the shins)
118
What are the most common causes of erythema nodosum?
Streptococcal infection, sarcoidosis, inflammatory bowel disease and drugs (penicillins, sulphonamides, COCP)
119
What is pretibial myxoedema?
Symmetrical, erythmatous lesions seen in Graves' disease | Shiny, orange peel skin
120
What is Necrobiosis Lipoidica Diabeticorum?
Shiny, painless areas of yellow/red skin typically on the shin of diabetics Often associated with telangiectasia
121
What are the three key skin malignancies?
Basal cell carcinoma Squamous cell carcinoma Malignant Melanoma
122
What is Kaposi sarcoma?
Tumour of vascular and lymphatic endothelium Purple cutaneous nodules Associated with immunosuppresion and HIV related disease
123
What is a dermatofibroma?
Benign lesion Firm elevated nodules Usually a history of trauma Lesion consists of histocytes, blood vessels and fibrotic changes
124
What skin disorders are associated with pregnancy?
Atopic eruption of pregnancy Polymorphic eruption of pregnancy Pemphigoid gestationis
125
What is atopic eruption of pregnancy?
Eczematous, itchy red rash. | No specific treatment is neeeded.
126
What is polymorphic eruption of pregnancy?
Pruritic condition assocaited with last trimester Lesions appear in abdominal striae Emolients, mild potency topical steroids, oral steroids
127
What is pemphigoid gestationis?
Pruritic blistering lesions Often develop in peri-unbilical region, spreads to trunk, back, buttocks and arms. Usually presents in 2-3rd treimester and rarely seen in 1st pregnancy Oral corticosteroids are usually required
128
What skin disorders are associated with SLE?
``` Photosensitive 'butterfly' rash Discoid lupus Alopecia Livedo reticularis: net-like rash Characteristic nasolabial sparing ```
129
What are the skin types?
Fitzpatrick Classification I: Never tans, always burns (often red hair, freckles, and blue eyes) II: Usually tans, always burns III: Always tans, sometimes burns (usually dark hair and brown eyes) IV: Always tans, rarely burns (olive skin) V: Sunburn and tanning after extreme UV exposure (brown skin, e.g. Indian) VI: Black skin (e.g. Afro-Caribbean), never tans, never burns
130
What are spider naevi?
(Spider angiomas) Describe a central red papule with surrounding capillaries. Blanch upon pressure Upper body.
131
How can spider naevi be differentiated from telangiectasia?
Pressing on them Spider naevi fill from the centre Twelangiectasia from the edge
132
What diseases are spider naevi seen in?
Liver disease Pregnancy COCP (10-15% of people will have one or more, common in childhood)
133
What are strawberry naevus?
(Capillary haemangioma) are usually not present at birth but may develop rapidly in the fist month of life. Erythmatous, raised and multilobed tumours. Typically increase in size until around 6-9 months before regressing over next few years.
134
What infants are more likely to have a strawberry naevus?
10% white infants Females Premature Mothers had chorionic villous sampling
135
What are the potential complications or strawberry naevus?
``` Mechanical e.g. obstructing visual fields or airway Bleeding Ulceration Thrombocytopaenia Cosmetic ```
136
What is the treatment of strawberry naevus if it is obstructive?
Propranolol
137
What is Tinea?
Dermatophyte fungal infections Tinea capitis - scalp Tinea corporis - trunk, legs or arms Tinea pedis - feed
138
What is Tinea capitis?
Scalp ringworm Cause of scarring alopecia mainly seen in children, if untreated a raised, pustular, spongy/boggy mass called a kerion may form.
139
What is tinea corporis?
Ringworm Causes (Trichophyton species) Well-defined annular, erythematous lesions with pustules and papules
140
What is the treatment of tine corporis (ringworm)?
Oral fluconazole
141
What is toxic epidermal necrolysis?
A potentially life-threatening skin disorder that is most commonly seen secondary to a drug reaction. Skin appears a scalded appearance over an extensive area. (TEN can be seen as severe end of a spectrum of skin disorders which includes erythema multiforme and SJS)
142
What are the features of toxic epidermal necrolysis?
Systemically unwell e.g. Pyrexia, tachycardia | Positive Nikolsky's sign: epidermis separates with mild lateral pressure
143
What drugs are known to induce toxic epidermal necrolysis?
``` Phenytoin Sulphonamides Allopurinol Penicillins Carbamazepine NSAIDs ```
144
What is the management of toxic epidermal necrolysis?
Stop precipitating factor Supportive care, often in ICE Intravenous immunoglobulin has been shown to be effective and now is commonly used first-line Other treatment options include: immunosuppressive agents (ciclosporin and cyclophosphamide), plasmapheresis
145
What are the large vessel vasculitides?
Temporal arteritis | Takayasu's arteritis
146
What are the medium vessel vasculitidis?
Polyarteritis nodosa | Kawasaki disease
147
What are the small vessel vasculitides?
ANCA-associated vasculitides (Wegener's, Churg-Strauss, microscopic polyangiitis) Henoch-Schonlein purpura Cryoglobulinaemic vasculitis
148
Where is venous ulceration most typically seen?
Above the medial malleolus
149
What are the investigations of leg ulcers?
Ankle-brachial pressure index (ABPI) | A 'normal' ABPI may be regarded as between 0.9-1.2
150
What is the management of venous leg ulcers?
Compression bandaging | Oral pentoxifylline
151
How can the rash seen in acne rosacea differentiate from the rash seen in SLE?
In SLE papules and pustules are rarely seen but in AR they are common
152
What antibody is most likely to be seen in dermatitis herpetiformis?
Anti-tissue transglutaminase antibody | Assocaited with coeliac disease