Passmedicine Flashcards
Erythema ab igne
Overexposure to infrared radiation
Features include reticulated, erythematous patches with hyperpigmentation and telangiectasia
If cause not treated then pt may go on to develop SCC
Linchen planus
Itchy papular rash - palms, soles, genitalia, flexor surfaces of arms.
Wickham’s striae - ‘white lace’ pattern on surface
Koebar phenomenon may be present - new skin lesions appearing at site of trauma
Oral involvement (50%). Nails - thinning of plate, longitudinal ridging
Gold, quinine, thiazides
Topical steroids. Oral steroids / immunosuppression if extensive.
Hereditary Haemorrhagic Telangiectasia
Autosomal dominant (20% no FHx)
Multiple telangiectasia over the skin and mucous membranes
2 (possible) / 3 (definite):
Epistaxis
Telangiectases
FHx (1st degree relative)
Visceral lesions e.g. GI telangiectasia, pulmonary / cerebral / hepatic / spinal AVM
Vitiligo
Autoimmune condition - loss of melanocytes and depigmentation of the skin
20-30 years
Well demarcated patches of depigmentation, peripheries mostly affected, Koebner phenomenon
Associated conditions - T1DM, Addison’s, pernicious anaemia, autoimmune thyroid disorders, alopecia areata
Sun block, camouflage make up, sun block (early), topical tacrolimus and phototherapy
Dermatitis herpetiformis
Autoimmune blistering skin disorder - IgA deposition in a granular pattern in the dermis
Associated with coeliac disease
Itchy, vesicular lesions on the extensor surfaces
Skin biopsy
Gluten free diet, dapsone
Hypertrichosis
Androgen-independent hair growth
Causes:
Drugs - minodixil, ciclosporin, diazoxide
Congenital hypertrichosis lanuginosa, congenital hypertrichosis terminalis
Porphyria cutanea tarda
Anorexia nervosa
Pytyriasis rosea
Acute, self limiting rash. Tends to affect young adults.
Herald patch (usually on trunk) followed by erythematous, oval, scaly patches (longitudinal diameters running parallel to the lines of Langerhan)
Usually disappears after 4-12 weeks
Herpes hominus virus 7 may play a role
Bullous pemphigoid
Autoimmune condition
Sub-epidermal blistering
Common in elderly patients
Features - itchy tense blisters typically around flexures, heal without scarring, mouth usually spared
Skin biopsy - immunofluorescence shows IgG and C3 at the dermoepidermal junction
Oral corticosteroids
Type 1 Hypersensitivity
Antigen reacts with IgE bound to mast cells
Anaphylaxis, atopy
Type 2 Cell bound
IgG or IgM reacts with antigen bound to cell surface
Autoimmune haemolytic anaemia, ITP, goodpasture’s, pernicious anaemia, acute haemolytic transfusion reactions, rheumatic fever, pemphigoid vulgaris / bullous pemphigoid
Type 3 Immune complex
Free antigen and antibody (IgA, IgG) combine
Serum sickness, SLE, post-streptococcal GN, extrinsic allergic alveolitis
Type 4 Delayed hypersensitivity
T cell mediated
TB / TB skin reactions, graft versus host disease, allergic contact dermatitis, scabies, extrinsic allergic alveolitis, MS, GBS
Type 5
Antibodies recognise and bind to cell surface receptors either stimulating them or blocking ligand binding
Graves’ disease, Myasthenia gravis
Pityriasis vesicolour
Superficial cutaneous fungal infection caused by Malassezia furfur
Features - most commonly affects trunk, patches may be hypopigmentates / pink / brown (may be more noticeable following a suntan), scale is common, mild pruritus
Healthy individuals, immunosuppression, Cushing’s, malnutrition
Topical antifungal (ketoconazole shampoo if extensive). Oral itraconazole.
Necrobiosis lipoidica diabeticorum
Shiny, painless areas of yellow / red skin typically on the shin of diabetics
Often associated with telangiectasia