DERMATOLOGY Flashcards
What are the common complications of seborrheoci dermatitis?
Otitis externa and blepharitis
Referral criteria to dermatology for acne?
Acne conglobate
Nodulo-cystic acne
Mild-mod acne not responded to 2 completed courses of Tx
Mod-sev acne not responded to a Tx including an oral antibiotic
Acne with scarring
Acne with persisting pigmentary changes
Acne causing persistent psychological distress
Which bacteria contributes to the development of acne?
Propionibacterium acnes
What drugs exacerbate psoriasis?
BB
Lithium
Antimalarials
NSAIDs
ACEi
Infliximab
Withdrawal of systemic steroids
What is hidradenitis suppurativa?
A chronic painful inflammatory skin disorder
Characterised by the development of inflammatory nodules, pustules, sinus tracts, and scars in intertriginous areas
Suspect in pts with recurrent furuncles or boils
Whats the most common site for hidradenitis suppurativa?
The armpit
Which drugs can cause erythema multiforme?
Penicillin
Sulphanoamides
Carbamazepine
Allopurinol
NSAIDs
COCP
Nevirapine
How long does it take the rash from pityriasis rosea to resolve?
6-12 weeks
Features of SCC?
typically on sun-exposed sites such as the head and neck or dorsum of the hands and arms
rapidly expanding painless, ulcerate nodules
may have a cauliflower-like appearance
there may be areas of bleeding
What virus causes molluscum contagious?
Pox virus
Does bullous pemphigoid or pemphigus vulgaris cause mucosal involvement?
Pemphigus vulgaris
What is pyoderma gangrenosum?
A rare, non-infectious inflammatory skin condition that cause very painful skin ulceration, usually on the legs
Causes of pyoderma gangrenosum?
Idiopathic 50%
IBD
RA, SLE
Haematological - lymphoma, myeloid leukaemias, myeloproliferative disorders etc
GPA
PBC
How does pyoderma gangrenosum present?
Sudden small red bump -> skin breaks down revealing a deep, necrotic, painful ulcer with purple edges
Bleeds easily if touched
May also cause fever and myalgia
What is this?
Pyoderma gangrenosum
What is hereditary haemorrhagic telangiectasia also known as?
Osler-Weber-Rendu syndrome
What are the 4 main diagnostic criteria for hereditary haemorrhagic telangiectasia?
Spontaneous, recurrent epistaxis
Telangiectasia at multiple sites - lips, oral cavity, fingers, nose
Visceral lesions: GI telangiectasia, hepatic AVM< cerebral AVM etc
First degree FHx of HHT
Most likely dermatological cancer when on immunosuppressives e.g. following renal transplantation?
SCC
What causes vitiligo?
Autoimmune condition causing loss of melanocytes and consequent depigmenattion of the skin
What conditions is vitiligo associated with?
Any autoimmune e..g T1DM, addisons, autoimmune thyroid, pernicious anaemia, Alopecia areata
Age of onset typical for vitiligo?
20-30