Porphyrias: a group of photosensitivity disorders resulting from an inherited or acquired defect in the enzymes required to produce adequate amounts of haem, with the subsequent accumulation of porphyrins
Main groups Phototoxic skin porphyria (e.g. erythropoietic protoporphyria) Blistering and fragility skin porphyrias Acute attack porphyrias (some with no skin involvement, some also cause blistering and fragility) Severe congenetial porphyria (e.g. congenital erythropoietic porphyria) Acute intermittent porphyria Most commonly presents in females around the age of 30 Enzyme deficiency - porphobilinogen deaminase Porphyrin accumulated - porphobilinogen Clinical p resentation Unlikely to actually present with cutaneous symptoms Porphyria cutanea tarda Most common type of porphyria Usually seen in middle aged men Commonly associated with liver disease, so often seen in those with haemochromatosis, hepatitis or alcohol misuse Enzyme deficiency - uroporphyrinogen decarboxylase Porphyrin accumulated - uroporphyrinogen Clinical p resentation Blistering lesions on sun exposed sites that heal with scarring and are associated with hyper pigmentation Also: hypertrichosis, solar urticaria, morphoea Investigations Bloods - porphyrin studies Woods lamp - urine shines pink instead of blue Management Establish and treat the underlying cause - alcohol, viral hepatitis, oestrogens, haemachromatosis Erythropeotic protoprophyria Most commonly seen in children Enzyme deficiency - ferrochelatase Porphyrin accumulated - protoporphyrin IX Clinical presentation There may be no evident rash but there will be burning and itching on the skin with sun exposure Typical presentation is child screaming when they are placed out in the sun Investigations Quantitative RBC porphyrins Flurocytes (patient, relatives) Management 6 monthy LFTs and RBC porphrins Visible light photoprotection measures Prophylactic TL-01 phototherapy Incipient liver failure - oral charcoal, cholestyramine, ASA synthase inhibition Liver failure - liver transplant Summary