In current textbooks of dermatology, lichen amyloidosus is said to be
a papular, intensely pruritic type of amyloidosis of unknown aetiology
. When this concept was developed, there was no way of discriminating
between the different types of amyloid. It is now known that amyloid i
n lichen amyloidosus is not derived from immunoglobulins or serum prot
eins, as it is in systemic amyloidoses, but from keratin peptides of n
ecrotic keratinocytes. Even several years ago, chronic scratching was
invoked as a possible cause of damage to keratinocytes in lichen amylo
idosus. In support of this hypothesis, four cases are presented. Apart
from amyloid in the papillary layer, all biopsy specimens revealed hi
stopathological signs of chronic scratching (epithelial hyperplasia wi
th hypergranulosis and compact orthokeratosis, coarse collagen in vert
ical streaks in the stratum papillare), such as are also found in prur
igo nodularis and lichen simplex chronicus. Lichen amyloidosus is cons
idered to be a variant of these conditions. Just as in prurigo nodular
is and lichen simplex chronicus, pruritus seems to be the cause and no
t a symptom of the papular skin lesions. Consequently, treatment of li
chen amyloidosus should not be directed at removing amyloid, but at im
proving the pruritus.