13.02.26 Psoriasis clinic
Drugs
Topical
Phototherapy
Psoralen + UVA (PUVA)
Methotrexate
Cyclosporine
Retinoids
Acitretin
Biologicals
Anti-TNF
Etanercept
Infliximab
Golimumab
Anti-IL-12/23
Ustekinumab
PASI score - Out of 72
Side-effects of biologicals
Malignancy
Lymphomas
Possibly melanomas
NOT benign tumours
Infection
cf Surgery
Side-effects of other systemics
MTX
Liver fibrosis
cf Alcohol contraindicated
Skin lymphoma
Reactivation of latent TB
Check specifically for symptoms + do CXR before starting
Risk of downward trend in lymphocytes
Cyclosporine => Renal damage
Pityriasis rosea
URTI may precede all other symptoms in as many as 69% of patients
A single, 2- to 10-cm oval red "herald" patch appears, classically on the abdomen
May occur in a 'hidden' position and not be noticed
7-14 days after the herald patch, large patches of pink or red, flaky, oval-shaped rash appear on the torso
In 6% of cases an inverse distribution may occur, with rash mostly on the extremities
The more numerous oval patches generally spread widely across the chest first, following the rib-line in a characteristic "christmas-tree" distribution
Small, circular patches may appear on the back and neck several days later
It is unusual for lesions to form on the face, but they may appear on the cheeks or at the hairline
About one in four people with PR suffer from mild to severe symptomatic itching
The rash may be accompanied by low-grade fever, headache, nausea and fatigue
Erythema multiforme
Skin condition of unknown cause
Possibly mediated by deposition of immune complex (mostly IgM) in the superficial microvasculature of the skin and oral mucous membrane that usually follows an infection or drug exposure
Common disorder; Peak incidence in the second and third decades of life
Presentation
Mild, self-limited rash to severe, life-threatening erythema multiforme major that also involves mucous membranes
May be related to Stevens–Johnson syndrome
Often takes on the classical "target lesion" appearance, with a pink-red ring around a pale center
Resolution within 7–10 days is the norm
Causes
Bacteria
BCG vaccination, haemolytic Streptococci, legionellosis, leprosy, Neisseria meningitidis, Mycobacterium, Pneumococcus, Salmonella, Staph, Mycoplasma pneumoniae, Chlamydia
Fungal
Parasitic
Trichomonas species, Toxoplasma gondii
Viral
Especially Herpes simplex
Drug reactions
Antibiotics (including sulphonamides, penicillin), anticonvulsants (phenytoin, barbiturates), aspirin, antituberculoids, allopurinol
Physical factors
Radiotherapy, cold, sunlight
Others
Collagen diseases, vasculitides, non-Hodgkin lymphoma, leukaemia, multiple myeloma, myeloid metaplasia, polycythemia
Post-inflammatory change
Ehlers–Danlos syndrome
Group of inherited connective tissue disorders caused by a defect in the synthesis of collagen (Type I or III)
Severity of the mutation can vary from mild to life-threatening
There is no cure, and treatment is supportive
Close monitoring of the digestive, excretory and particularly the cardiovascular systems
Physical therapy, bracing, and corrective surgery may help with the frequent injuries and pain that tend to develop in certain types of EDS
Notes
Hydroxychloroquine
SLE
RA
Sjögren's
Porphyria cutanea tarda
Mycophenolate mofetil
For eczema, not psoriasis
Stopping and starting biologicals can => anti-drug antibodies
But must stop 1 month pre-surgery due to infection risk
DLQU index
Link between psoriasis + metabolic syndrome/weight gain