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Cancer Control. 2016 Apr;23(2):170-4. doi: 10.1177/107327481602300213.

Pathology Report: Presacral Noncommunicating Enteric Duplication Cyst.

Cancer control : journal of the Moffitt Cancer Center

Shabnam Seydafkan, David Shibata, Julian Sanchez, Nam D Tran, Marino Leon, Domenico Coppola

Affiliations

  1. Department of Anatomic Pathology, Moffitt Cancer Center, Tampa, FL 33612, USA. [email protected].

PMID: 27218796 DOI: 10.1177/107327481602300213

Abstract

BACKGROUND: Gastrointestinal (GI) tract duplication cysts or enteric duplication cysts are rare congenital malformations sometimes found on the mesenteric aspect of segments of the alimentary tract. Enteric duplication cysts are lined by normal GI epithelium and may be classified as foregut, mid-gut, and hindgut cysts. Except in very rare cases of retroperitoneal enteric duplication cysts, these cysts communicate with the GI tract and share a common blood supply. Concurrent congenital malformations are not uncommon and malignant transformation within enteric duplication cysts has also been reported.

METHODS: We describe a case of a noncommunicating enteric duplication cyst in a 52-year-old woman.

RESULTS: The patient presented with a presacral cystic mass requiring frequent drainage procedures that was primarily believed to be of neural origin. Upon resection, the lesion contained heterotopic tissue, including ciliated bronchial epithelium, squamous and transitional epithelia, and pancreatic and gastric tissue. Focal, low-grade intestinal adenoma was present, but malignancy was not detected in this case.

CONCLUSION: To our knowledge, this is the sixth reported case of a noncommunicating enteric duplication cyst in the English medical literature.

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