Myocarditis and coronary dilatation in the 1st week of life: neonatal incomplete Kawasaki disease?

Details

Serval ID
serval:BIB_20DC4CBD6297
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
Title
Myocarditis and coronary dilatation in the 1st week of life: neonatal incomplete Kawasaki disease?
Journal
European journal of pediatrics
Author(s)
Bolz D., Arbenz U., Fanconi S., Bauersfeld U.
ISSN
0340-6199
Publication state
Published
Issued date
1998
Peer-reviewed
Oui
Volume
157
Number
7
Pages
589-91
Language
english
Notes
Publication types: Case Reports ; Journal Article - Publication Status: ppublish
Abstract
Acute heart failure in the early neonatal period is rare. Normally it is due to asphyxia, severe septicaemia, a congenital heart malformation or a viral myocarditis. Kawasaki disease (KD) as a cause of an neonatal myocarditis is not an established diagnosis. KD is a vasculitis of still unknown origin occurring predominantly in infants and preschool children. KD before the age of 3 months is rare. There are only few reports about KD in the 1st month. We present a newborn who showed the cardiac symptoms of KD in the 1st week of life with coronary dilatation and myocarditis. CONCLUSION: The diagnosis of incomplete KD should be considered not only in infants but also in newborns with signs of myocarditis and coronary abnormalities. Therapy with gammaglobulins may prevent the sequelae of coronary involvement.
Keywords
Coronary Disease, Humans, Infant, Newborn, Male, Mucocutaneous Lymph Node Syndrome, Myocarditis
Pubmed
Web of science
Create date
25/01/2008 11:06
Last modification date
20/08/2019 13:57
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