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DOI: 10.1055/a-2094-9279
Endoscopic resection for an esophageal inclusion cyst
Supported by: 1·3·5 project for disciplines of excellence, West China Hospital, Sichuan University ZYJC21011
A 24-year-old woman complained of intermittent dysphagia for 2 years. She reported a previous medical history of asthma, hyperthyroidism, and myocarditis. Physical examination revealed no special abnormalities. Computed tomography detected a 5.2 × 4.2-cm mass with a clear boundary in the esophagus ([Fig. 1 a]). Endoscopy showed a large lesion 30–34 cm from the incisors ([Fig. 1 b]). Endoscopic ultrasonography confirmed the hypoechoic lesion with hyperechoic foci, originating from the submucosal layer ([Fig. 1 c]). Endoscopic resection was performed for this patient ([Fig. 2], [Video 1]). After submucosal injection at 3 cm proximal to the lesion, a mucosal incision was made using a dual knife. A submucosal tunnel was subsequently created. When the lesion was partially exposed with an insulated-tip knife, it ruptured suddenly and yellow milky fluid flowed out, suggesting an esophageal cyst. The top layer of the cyst was resected using the dual knife. Then, the remaining rest cyst wall was destroyed using electrocoagulation forceps and anhydrous alcohol. The mucosa beyond the cyst was also removed using a snare. There was no bleeding or perforation during the procedure. Histopathology showed a pseudostratified ciliated columnar epithelium-lined cyst wall and no cartilage or bilayer smooth muscle, confirming it was esophageal inclusion cyst. The patient recovered uneventfully. During 2 months of follow-up, the patient reported no further discomfort; endoscopy also showed complete healing of the wound ([Fig. 3]).




Video 1 Endoscopic resection for an esophageal inclusion cyst.
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Esophageal cysts are rare, with an incidence of one in 8200 [1]. Compared with duplication and bronchogenic cysts, an inclusion cyst is characterized by the absence of bilayer smooth muscle and cartilage [2]. All these esophageal cysts are usually benign and asymptomatic, but they may cause dysphagia. In addition, malignant transformation of esophageal cysts has also been reported [3]. Removal of esophageal cysts usually completely relieves symptoms or complications. The key point is to completely remove the entire cyst wall to prevent recurrence.
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Competing interests
The authors declare that they have no conflict of interest.
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References
- 1 Vougiouklakis T, Mitselou A, Dallas P. et al. Inclusion cyst of esophagus: Case report and review of the literature. Exp Oncol 2003; 25: 22-24
- 2 Kolomainen D, Hurley PR, Ebbs SR. Esophageal duplication cyst: case report and review of the literature. Dis Esophagus Off J Int Soc Dis Esophagus 2017; 11: 62-65
- 3 Wan Abdul Rahman WF, Mutum SS, Fauzi MH. Keratinous inclusion cyst of oesophagus: unusual finding. BMJ Case Rep 2013; 2013: bcr2013010172
Corresponding author
Publication History
Article published online:
15 June 2023
© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
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References
- 1 Vougiouklakis T, Mitselou A, Dallas P. et al. Inclusion cyst of esophagus: Case report and review of the literature. Exp Oncol 2003; 25: 22-24
- 2 Kolomainen D, Hurley PR, Ebbs SR. Esophageal duplication cyst: case report and review of the literature. Dis Esophagus Off J Int Soc Dis Esophagus 2017; 11: 62-65
- 3 Wan Abdul Rahman WF, Mutum SS, Fauzi MH. Keratinous inclusion cyst of oesophagus: unusual finding. BMJ Case Rep 2013; 2013: bcr2013010172





