Dermatology Flashcards
(170 cards)
What is bullous pemphigoid
Autoimmune sub-epidermal condition characterised by large, tense blisters found on the limbs, trunks and flexors
Bullae/erosions may be also found on oral/genital mucosa
What autoantibodies are present in bullous pemphigoid
BP antigen II and I
Treatment of bullous pemphigoid
Steriods
Supportive measures
Risk factors for developing bullous pemphigoid
Previous chronic inflammatory skin conditions (e.g. lichen planus or psoriasis)
Drugs
- furosemide
- antibiotics
- NSAIDs
Neurological disease
- PD
- dementia
- Epilepsy
Causes of bullous eruptions
Congenital
Strep infection
Staph scalded skin syndrome
TEN
Diabetic bullae
CKD
Haemodialysis
Barbituate overdose
Immunological
What is erythema multiforme?
Presents as eruptions of multiple lesions, which are maculopapular, target shaped rashes but can appear in various forms (hence the name multiforme)
Where can erythema multiforme occur?
Anywhere on the body
Palms
Soles
Oral mucosa
What may there be a history of with erythema multiforme?
Viral illness
Where does the rash usually start and spread with eyrthema multiforme?
Starts distally
Spreads proximally
What is Koebeners phenomenon?
Lesions appearing on areas of previous skin trauma
Differentials of erythema multiforme
Insect bites
SJS
TEN
Drug eruption
Dermatitis
Bullous pemphigoid
Pemphigus
Dermatitis herpetiformis
What is neurofibromatosis?
A genetic condition characterised by lesions of the skin, CNS and skeleton
Types of neurofibromatosis
Type I
Type II
Schwannomatosis
Genetics of neurofibromatosis type I
Autosomal dominant inherited disorder
Caused by mutation in the neurofibromin gene (NF1) on chromosome 17
Presentation of NF1
Often presents in first year of life and increase in number with age
Leads to multiple tumours that grow along the NS anywhere in the body
Skin lesions
- multiple neurofibromas (skin coloured lesions) and cafe au lai macules
- freckling, particularly in skin folds
Neuro dermatofibromas arise from nerve trunks and can cause paraesthesia when pressed
Lisch nodules (seen on eye with slit lamp)
Short stature
Macrocephaly
Around 30% develop
- Mild learning disability
- Acoustic neuromas
- epilepsy
Rare assosiation of NF1
Phaechoromocytoma
Main difference NF2 vs NF1
CNS tumours being more characteristic than skin lesions
Presentation of NF2
Bilateral acoustic neuromas are characteristic
Meningiomas
Glial cell tumours
Usually present with deafness in their 20s; tinnitus, veritgo
Genetics of NF2
Mutation found on chromosome 22
Can be autosomal dominance or de novo (up to 50%)
Treatment of acoustic neuroma
Surgical excision
Mean survival from diagnosis of NF2
15 years
What is schwannomatosis?
Occurence of multiple tender cutaneous schwannomas without the vestibular neuroma assosiated with NF2
Often a very large tumour load requiring assessment with MRI
Is life expectancy affected in schwannomatosis?
No
Which NF is more common?
Type 1