Duplication of the esophagus has a range of macroscopic appearances from complete (very rare) to partial cystic duplication (esophageal duplication cyst). It is the second most common gastrointestinal tract duplication after that of the ileum.
A complete duplication is a rare malformation and is also often associated with a gastric duplication (also rare). A partial duplication is more common. As a congenital abnormality, it is usually identified soon after birth, if symptomatic.
Presentation of large duplication cysts usually occurs in the newborn or infant, with symptoms referable to pressure on the adjacent lung or esophagus, leading to:
- respiratory difficulties
Smaller cysts can be asymptomatic and are usually found incidentally at imaging.
The duplicated segment has a thick wall of smooth muscle and is lined with alimentary tract mucosa. The lining mucosa may be the same as that in the segment it parallels, or may be similar to the mucosa lining some other portion of the alimentary tract - frequently, gastric mucosa, in which case peptic ulceration of the duplication is a common finding.
Most often, duplications are spherical cysts that rarely make an impression on the esophagus and are usually located in the right hemithorax.
On plain chest radiographs, they are usually seen as rounded fluid / soft tissue density posterior mediastinal masses.
In cystic esophageal duplication, the esophagogram shows the esophagus to be displaced to the side opposite the mass (i.e. contralaterally).
Duplication cysts appear as sharply marginated masses with homogeneous fluid density. No enhancement is visible after intravenous contrast administration.
MRI demonstrates features of a cyst. Signal characteristics therefore include:
- T1: low signal
- T2: high signal
- T1 C+ (Gd): no solid enhancement
- neoplasms arising from the sympathetic chain: ganglioglioma, ganglioneuroma, etc
- the distinction between this entity and esophageal duplication cysts is often impossible on imaging alone, and can only be settled by obtaining histology, which is not normally done
- furthermore, in asymptomatic patients the distinction is of no real clinical relevance
- pericardial cyst
- neurenteric cyst
- pulmonary sequestration
- anterior meningocele
- 1. Berrocal T, Madrid C, Novo S et-al. Congenital anomalies of the tracheobronchial tree, lung, and mediastinum: embryology, radiology, and pathology. Radiographics. 24 (1): e17. doi:10.1148/rg.e17 - Pubmed citation
- 2. Jeung MY, Gasser B, Gangi A et-al. Imaging of cystic masses of the mediastinum. Radiographics. 2002;22 Spec No (suppl 1): S79-93. Radiographics (full text) - Pubmed citation
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