| Literature DB >> 17594109 |
A Espeso1, S Verma, P Jani, H Sudhoff.
Abstract
Foregut duplication cysts are rare congenital anomalies of enteric origin. The diagnosis is usually made in infancy. We report the unusual case of a 71-year-old female presenting to the ENT department with shortness of breath and stridor due to an oesophageal reduplication cyst. The presentation, diagnosis and management of this potential pitfall for the unwary are outlined.Entities:
Mesh:
Year: 2007 PMID: 17594109 DOI: 10.1007/s00405-007-0364-3
Source DB: PubMed Journal: Eur Arch Otorhinolaryngol ISSN: 0937-4477 Impact factor: 2.503