Dermatological presentations of systemic disease Flashcards
Erythema nodosum
A: Inflammation of fat cells beneath the skin
Can be from autoimmune (IBD, Bachet’s), Drugs (OCP, sulphonamides), idiopathic, infection (strep, TB, hep C), malignancy, pregnancy, sarcoidosis
S: Red, tender nodules or lumps, usually on the shins
D: Underlying cause
T: Self-limiting, so focus on alternative cause. If it doesn’t improve potassium iodide can be given.
Pyoderma gangenosum
A: Neutrophilic disorder causing skin ulceration.
Thought to be autoimmune and associated with IBD, rheumatoid arthritis and haematological disorders (myeloma).
S: Begins as a small pustule then rapidly ulcerates. Ulcers rapidly grow in size and are usually painful with a purple border. Usually lower limbs.
D: Underlying cause
T: Topical or systemic steroids
Dermatitis Herpetiformis
A: Skin manifestation of coeliac disease.
S: Intensely itchy rash, commonly on extensor surfaces.
D: Skin biopsy shows IgA
T: Gluten free diet, dapsone for itching/blistering, steroids may be needed.
Erythema multiforme
A: Hypersensitivity reaction usually triggered by an infection. Herpes simplex and mycoplasma pneumonia are the commonest cause.
Other causes include drugs (antibiotics, sulphonamides), infection (EBV, hep B, histoplasmosis), lupus, malignancy, pregnancy, sarcoidosis.
S: Target lesions - well demarcated, round, pink, flat lesions, which become raised to form a plaque with a pale ring around the centre.
D: Clinical
T: Self-limiting
Acanthosis nigricans
A: Common causes include insulin resistance, obesity, PCOS and paraneoplastic (from GI malignancy).
S: Brown hyperpigmentation of the skin, commonly at groin or axilla.
D: Underlying cause
T: Underlying cause
Thrombophlebitis migrans
A: Paraneoplastic syndrome often from pancreatic or lung malignancy.
S: Recurrent thrombophlebitis.
Tender, palpable blood vessels with overlying redness and swelling.
D: Can be confirmed by Doppler studies, but investigation of malignancy is needed.
T: Rest, elevation, compression stockings, NSAIDs.
Lupus vulgaris
A: Persistent and progressive cutaneous manifestation of mycobacterium tuberculosis.
S: Small, sharply defined reddish-brown lesions with a gelatinous consistency.
D: Confirm with skin biopsy
T: TB treatment
Lupus pernio
A: Cutaneous manifestation of sarcoidosis
S: Large, bluish-red/purple nodules on face, hands or feet.
D: Skin biopsy shows granulomatous infiltration.
T: Sarcoidosis treatment.
Necrobiosis lipoidica
A: Rare skin disorder that affects the shins of insulin-dependent diabetics.
S: Yellow/brown, waxy patches on the shins. Typically painless and slowly growing.
D: -
T: Topical steroids, intralesional steroid injections, aspirin and dipyridamole, ciclosporin or PUVA treatment.
Granuloma annulare
A: Chronic skin disease caused by granulomatous inflammation occurring withing the dermis. Usually idiopathic but can be associated with autoimmune diseases (DM, thyroid, SLE) or malignancy.
S: Usually a ring of small, red papules over backs of forearms, hands or feet with a tendency to joints or knuckles. May be tender if knocked.
D: Skin biopsy can confirm if needed
T: Often resolve spontaneously. But can give topical, intralesional or systemic steroids, topical iniquimod or tacrolimus.