Prenatal diagnosis and management of congenital subglottic stenosis associated with congenital esophageal atresia type C

Tomoyuki Sato, Masaki Nio, Hiromu Tanaka, R. Ohi

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Most patients with congenital esophageal atresia (EA) have congenital tracheobronchial abnormalities, which may cause respiratory distress, be difficult to treat and have a poor prognosis. The authors report a neonate with EA and congenital subglottic stenosis (SGS) who exhibited severe respiratory distress immediately after birth. After emergency endotracheal intubation with a narrow endotracheal tube, the authors performed total correction of EA and anterior cricoid split (ACS) on day 1 of age. The postoperative course was uneventful. Some reports have stated that it is difficult to make a prenatal diagnosis when SGS is associated with EA and tracheoesophageal fistula (TEF). The anterior cricoid split technique may be suitable for managing moderate SGS even in neonates with EA. Partial resection of the hypertrophic cricoid cartilage is considered effective in preventing restenosis.

Original languageEnglish
Pages (from-to)131-133
Number of pages3
JournalEuropean Journal of Pediatric Surgery
Volume18
Issue number2
DOIs
Publication statusPublished - 2008 Apr 1
Externally publishedYes

Keywords

  • Congenital esophageal atresia (EA)
  • Congenital subglottic stenosis (SGS)
  • Neonate
  • Prenatal diagnosis

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Surgery

Fingerprint Dive into the research topics of 'Prenatal diagnosis and management of congenital subglottic stenosis associated with congenital esophageal atresia type C'. Together they form a unique fingerprint.

Cite this