Congenital Vascular Anomalies Causing Tracheoesophageal Compression
- 1 February 1984
- journal article
- research article
- Published by American Medical Association (AMA) in JAMA Otolaryngology–Head & Neck Surgery
- Vol. 110 (2) , 82-87
- https://doi.org/10.1001/archotol.1984.00800280016006
Abstract
• Congenital vascular anomalies of the great vessels causing marked tracheoesophageal compression are rare. Notable symptoms usually manifest in the neonatal period and include stridor, repeated cyanotic attacks, recurrent pneumonia, and dysphagia. Although the diagnosis can often be made from barium swallow studies, the preoperative examination should nevertheless include an endoscopy. This is essential if the degree of tracheomalacia is to be adequately assessed and other tracheobronchial abnormalities are to be identified. Possible airway problems can then be anticipated, thus minimizing postoperative respiratory difficulties. (Arch Otolaryngol 1984;110:82-87)This publication has 2 references indexed in Scilit:
- THORACIC SURGERY FOR INFANTSThe Journal of Thoracic and Cardiovascular Surgery, 1964
- Surgical Relief for Tracheal Obstruction from a Vascular RingNew England Journal of Medicine, 1945