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Archives of Disease in Childhood - Fetal and Neonatal Edition 1999;81:F134-F137; doi:10.1136/fn.81.2.F134
Copyright © 1999 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.
Arch Dis Child Fetal Neonatal Ed 1999;81:F134-F137 ( September )

Neonatal neuroblastoma

J Moppett, I Haddadin, A B M Foot, on behalf of the United Kingdom Children's Cancer Study Group

The Royal Hospital for Sick Children St Michael's Hill Bristol BS2 8BJ

Correspondence to: Dr J Moppett.

Accepted 17 March 1999

Over nine years, 33 children with neonatal neuroblastoma were registered with the UKCCSG (United Kingdom Children's Cancer Study Group). Tumours of all stages were found, but stage 4S disease predominated. Five tumours were detected prenatally by ultrasonography. Treatment varied according to tumour stage. The overall survival of the group was 91%. Ten children have had long term complications as a result of their disease, usually as a result of spinal tumour involvement. The good overall prognosis in this age group is encouraging, but the poor neurological outcome of patients with intraspinal extension is of concern.


Keywords: neurological outcome; tumour stage; neuroblastoma


© 1999 by Archives of Disease in Childhood

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This article has been cited by other articles:

  • Holzer, R, Franklin, R C G (2002). Congenital heart disease and neuroblastoma: just coincidence?. Arch. Dis. Child. 87: 61-64 [Abstract] [Full Text]  

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