KAWASAKI-DISEASE IN A SUDANESE FAMILY

Authors
Citation
A. Elamin, KAWASAKI-DISEASE IN A SUDANESE FAMILY, Annals of tropical paediatrics, 13(3), 1993, pp. 263-268
Citations number
NO
Categorie Soggetti
Pediatrics,"Tropical Medicine
ISSN journal
02724936
Volume
13
Issue
3
Year of publication
1993
Pages
263 - 268
Database
ISI
SICI code
0272-4936(1993)13:3<263:KIASF>2.0.ZU;2-H
Abstract
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.