An association of non-specific signs: Described in Japan in 1967, Kawa
saki syndrome (adeno-cutaneo-mucosal syndrome) is an acute systemic va
sculitis oi unknown origin. The condition is specific to children with
characteristic fever cutaneo-mucosa involvement and cervical node enl
argement Cardiovascular complications predominate (myocarditis, perica
rditis and coronary aneurysms in 20% of the non-treated cases). Intrav
enous immunoglobulins is the preferred treatment. Specific cases in ad
ults: Sixty-four cases have been reported in adults. The main clinical
features are the same as in children, but digestive disorders, hepati
c involvement and joint disease are more frequent in adults. Severe co
mplications: As in children severe complications may occur. Four adult
s have developed coronary aneurysms, three have had aneurysms of visce
ral arteries and one died from encephalitis. (C) 1998, Masson, Paris.