Case report: Antenatal MRI diagnosis of esophageal duplication cyst

Abstract Esophageal duplication cysts are classified as a subgroup of foregut duplication cysts. They are very rare and are predominantly detected in children. Antenatal detection is very rare. We report a case of an esophageal duplication cyst that was accurately identified antenatally by USG and MRI.

right paravertebral gutt er in the upper thorax and was prevertebral in the lower thorax.There was no spinal abnormality, and no intraspinal extension was seen.A radiological diagnosis of esophageal duplication cyst was made.
One week later the fetus was delivered by an elective Caesarean section.The neonate had persistent tachypnea.No cardiac anomaly was seen on echocardiography.A CT scan of the thorax was performed and the scannogram showed a right-sided mediastinal opacity [Figure 3A].Axial sections showed an elongated, cystic lesion in the posterior mediastinum, extending from the thoracic inlet into the abdominal cavity up to the L 1 level [Figure 3B-D].The lesion was in the right paravertebral gutt er in the upper thorax and was prevertebral in the lower thorax and upper abdomen.It was posterior to the esophagus in the lower thorax.No spinal anomalies were present.
On the Þ ft h day of life, the neonate underwent a right anterolateral thoracotomy.The cyst was dissected from the adjacent tissues and totally excised.The child recovered uneventfully.Histopathological examination showed gastric-type mucosa with well-developed submucosa, muscularis propria, and serosa [Figure 4].There was no cell atypia to suggest malignancy.These Þ ndings conÞ rmed the radiological diagnosis.

Discussion
Several theories have been proposed to explain the origin Article published online: 2021-07-31 of duplications in the gastrointestinal tract. [1]The 'split notochord theory' postulated by Bentley and Smith is the most accepted explanation for foregut duplications. [1,5]uring the third week of intrauterine life the notochord fuses with the embryonic ectoderm and at about the fourth week, the endoderm separates from the notochord.Duplication cysts and vertebral defects can occur if adhesions or a neuroenteric band persist aft er this separation. [5]When foregut cysts are associated with vertebral anomalies they are called neuroenteric cysts.Pathologically, mediastinal cysts are called esophageal duplication cysts if they are close to the esophageal wall; are covered by two muscle layers; and if the lining is squamous, columnar, cuboid, pseudostratiÞ ed, or ciliated epithelium. [3,6] esophageal duplication cyst commonly presents with respiratory distress in infancy and childhood.It may be asymptomatic in adulthood or may present with dysphagia. [1]Bleeding can occur within the cyst when there is gastric mucosa.The cyst may enlarge in size due to retention of secretions and produce mass eff ect.Sometimes cysts may be complicated by malignant transformation or ulceration or they may rupture, with consequent mediastinitis and peritonitis. [7] 495 duplications reviewed by Nawaz et al, [1] and Stringer et al, [8] midgut duplications accounted for 50%, foregut duplications for 36%, and hindgut duplications for 12% of cases.Esophageal duplications accounted for 19%. [8]On  antenatal USG, esophageal duplication cysts are seen as posterior mediastinal cysts and appear as smooth, spherical, or tubular structures with well-deÞ ned walls.There may be layering of debris or septal folds within the cyst.The two layers of the wall-an inner echogenic mucosal layer and a hypoechoic outer muscular layerare seen in 50% of lesions postnatally. [7]The cyst may be thoracoabdominal if very large.Antenatal MRI is very useful for further evaluation as it can show abdominal extension bett er.Because of the watery content of the cyst it appears hyperintense on T2W images. [2]A right-sided or posteroinferior mediastinal location favors the diagnosis of an esophageal duplication cyst. [2]The wall is relatively thicker than that of a bronchogenic cyst. [2]Continuity with the spine, if present, can also be demonstrated by MRI.
Postnatal chest radiographs may show a posterior mediastinal opacity.CT scan helps in delineating the size, location, extent, and the anatomic association of the mass to other organs.The adjacent lung can also be assessed on CT scan.MRI is also useful in characterizing the cyst and for ruling out spinal communications.The diff erential diagnoses include other foregut cysts, e.g., bronchogenic cyst and neuroenteric cyst. [2,9]Bronchogenic cysts are usually located around the tracheobronchial tree.Neuroenteric cysts have some communication with the spine.A well-deÞ ned, circular vertebral defect in the midst of a complex vertebral anomaly favors the diagnosis of a neuroenteric cyst [10] ; this defect represents a connecting stalk between the mediastinal cyst and the intraspinal extension.Some authors advocate only observation in smaller and asymptomatic cysts. [2]However, because of the potential for complications, complete excision of the cyst is the treatment of choice. [1]

Figure 4 :
Figure 4: Histopathologic section of the cyst wall shows gastric-type mucosa (arrows) with a thick muscular layer (arrowheads)