| Literature DB >> 1780740 |
E Santoli1, P Di Biasi, P Vanelli, C Santoli.
Abstract
Congenital tracheal obstruction, though not notably uncommon in infancy, is rarely due to isolated tracheomalacia, especially when characterized by complete absence of cartilaginous rings. A 5-year-old boy underwent successful tracheal resection and anastomosis following severe tracheal obstruction due to aplasia of cartilaginous rings.Entities:
Mesh：
Year: 1991 PMID： 1780740 DOI： 10.3109/14017439109099044
Source DB: PubMed Journal: Scand J Thorac Cardiovasc Surg ISSN： 0036-5580