Actinic prurigo (AP) belongs to the group of idiopathic photodermatose
s sharing a predilection for occurring more commonly in females, and t
here is much controversy as to whether it is only a more severe form o
f polymorphous light eruption (PMLE) or whether it is a distinct entit
y in its own right. The condition is characterised by intensely itchy
papules, plaques and nodules, along with excoriations and scars usuall
y starting before puberty, and predominantly involves the sun-exposed
areas although it may also affect covered sites. Seasonal exacerbation
s at the beginning of spring with improvement in the fall are typical,
although the lesions frequently do not clear completely in the winter
. The disorder may run a chronic course and persist into adulthood, bu
t often spontaneous resolution occurs in late adolescence. Diagnosis i
s predominantly based on the clinical features, cutaneous irradiation
tests and histology often being normal or non-specific. HLA typing has
also been performed in both PMLE and AP patients, showing a strong as
sociation between HLA-DR4, in particular with the DRB10407 subtype, a
nd AP; no HLA association has been found in PMLE. This HLA association
is likely to be of pathogenic significance and strongly suggests a cr
itical role for MHC-restricted antigen presentation in the development
of photosensitivity AP.