| Literature DB >> 3351729 |
B A Michna1, N B McWilliams, T M Krummel, M A Hartenberg, A M Salzberg.
Abstract
Neuroblastoma and Hirschsprung's disease are considered aberrations of neural crest cell growth, migration, or differentiation. Their coexistence, however, is rare. We present the case of an only child with total colon Hirschsprung's disease diagnosed shortly after birth, who was found to have noncontiguous ganglioneuroblastomas without metastases at age 16 months. The spectrum of neural crest anomalies, long segment Hirschsprung's disease and multifocal neuroblastoma, in this child is unique and previously unreported.Entities:
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Year: 1988 PMID: 3351729 DOI: 10.1016/s0022-3468(88)80541-4
Source DB: PubMed Journal: J Pediatr Surg ISSN: 0022-3468 Impact factor: 2.545