Kawasaki disease (mucocutaneous lymph node syndrome) is an acute infla
mmatory multisystem disease of children. The acute phase of the diseas
e is characterized by high grade fever, conjunctivitis, exanthematous
skin rash and non-suppurative lymph node enlargement. The subacute pha
se follows with the manifestations of arthritis, myocarditis and throm
bocytosis. The disease is self-limiting in most children but is associ
ated with coronary artery aneurysms in 15-20% of cases. The aetiology
is unknown, but results of epidemiological studies suggest that an uni
dentified infectious agent might be the causative factor. Since the fi
rst description of the disease by the Japanese doctor, Tomisaku Kawasa
ki, in 1967 and his report for the English literature in 1974, thousan
ds of cases have been reported worldwide. The highest prevalence is fo
und in Japan and among the Japanese in Hawaii, followed by the United
States. Although the disease was first reported in Africa in 1979, to
date only four cases have been reported there. The following account r
eviews the literature and describes the manifestations of Kawasaki dis
ease as seen in two siblings in Khartoum, Sudan.