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PMID: 7472988 Published · ppublish English Case Reports Journal Article

The complete spectrum of neurocristopathy in an infant with congenital hypoventilation, Hirschsprung's disease, and neuroblastoma.

Journal of pediatric surgery ·Vol. 30 ·No. 8 ·1995-08-00 ·Pages 1218-21

Stovroff M, Dykes F, Teague WG

Abstract

Neuroblastoma, Hirschsprung's disease, and central hypoventilation (Ondine's curse) are considered aberrations of neural crest cell growth, migration, or differentiation, and as such are considered to be under the general heading of neurocristopathy. Their combined occurrence in a newborn infant presenting with total colonic aganglionosis, central hypoventilation, and multifocal neuroblastoma had not been reported previously. A 2.3-kg white full-term girl required endotracheal intubation because of persistent apnea in the first hours of life. She had progressive abdominal distension and failure to pass meconium; a barium enema was performed, which showed microcolon with meconium pellets at the distal ileum. During laparotomy the distal ileum was found to be obstructed with inspissated meconium; an ileostomy and appendectomy were performed. The resected specimens were aganglionic. An additional 20 cm of aganglionic ileum was removed, and a normally innervated ileostomy was constructed. Numerous attempts at extubation failed because of apnea. The results of an extensive apnea workup, including electroencephalogram, magnetic resonance imaging (MRI), bronchoscopy, and pH probe study, were normal. Sleep studies showed congenital central hypoventilation syndrome, and the patient underwent a tracheostomy. At 3 months, an abdominal ultrasound examination performed within a septic workup showed a right suprarenal mass extending across the midline. Thoracic and abdominal MRI scans showed large bilateral adrenal and posterior mediastinal masses. The serum catecholamines and ferritin level were markedly elevated, suggestive of neuroblastoma. In light of the child's multiple problems, the family chose to forgo further workup (including a tissue biopsy) and therapy. In the following 2 months her tumor load rapidly progressed, and she died of respiratory insufficiency.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Adrenal Gland Neoplasms/complications,congenital Colonic Diseases/complications,congenital,surgery Female Follow-Up Studies Hirschsprung Disease/complications,surgery Humans Ileal Diseases/etiology Infant, Newborn Intestinal Obstruction/etiology Meconium Mediastinal Neoplasms/complications,congenital Neural Crest/pathology Neuroblastoma/complications,congenital Sleep Apnea Syndromes/complications,congenital,surgery Tracheostomy
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Stovroff M
Division of Pediatric Surgery, Emory University School of Medicine, Atlanta, GA 30322, USA.
Dykes F
Teague W G
Article Info
Journal
Journal of pediatric surgery
Abbr.
J Pediatr Surg
ISSN
0022-3468
Published
1995-08-00
Pages
1218-21
Language
English
Region
United States
NLM ID
0052631
Subset
IM
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