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Case Report
- Completely Isolated Enteric Duplication Cyst Presenting as an Inguinal Hernia.
- Jung Uee Lee, Jong Ok Kim, Say June Kim, Hye Jung Sul
- Korean J Pathol. 2010;44(2):204-206.
- DOI: https://doi.org/10.4132/KoreanJPathol.2010.44.2.204
- 3,372 View
- 31 Download
- 4 Crossref
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Abstract
PDF - Enteric duplication cysts are uncommon congenital anomalies whose embryogenesis remains unknown. We report here on an isolated enteric duplication cyst, that presents as an inguinal hernia. A 21-year-old woman was admitted with a month-long history of a palpable mass in the left groin. Radiologically, a computed tomography scan revealed a 3.5 x 2.5 cm sized cystic mass in subcutaneous layers of the left suprapubic area. Microscopically, the cystic wall resembled gut wall. The wall was composed of two distinct muscle layers with the presence of Auerbach's plexus. On examining the entire sections of the cyst wall very carefully, no epithelial lining was found on the inner surface. The submucosa was slightly fibrotic. The diagnosis was a completely isolated enteric duplication cyst.
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Citations
Citations to this article as recorded by
- A case of completely isolated advanced enteric duplication cyst cancer performed partial pancreatectomy
Shinsuke Nakashima, Terumasa Yamada, Go Sato, Takaaki Sakai, Yoshinao Chinen, Hiroaki Itakura, Ryo Kato, Masami Ueda, Yujiro Tsuda, Katsuya Ohta, Jin Matsuyama, Masakazu Ikenaga
International Journal of Surgery Case Reports.2019; 54: 83. CrossRef - A huge completely isolated duplication cyst complicated by torsion and lined by 3 different mucosal epithelial components in an adult
Ai Xiao-Ming, Lu Jin-Jing, Ho Li-Chen, Han Lu-Lu, Yue Xiong, Zhang Hong-Hai, Yang Nian-Yin
Medicine.2018; 97(44): e13005. CrossRef - An isolated intestinal duplication cyst masquerading as a mucinous cystic neoplasm of the pancreas
Evan Weitman, Sameer Al Diffalha, Barbara Centeno, Pamela Hodul
International Journal of Surgery Case Reports.2017; 39: 208. CrossRef - Isolated omental duplication cyst with respiratory epithelium & pancreatic glands: Case report & review of literature
Phuoc T. Nguyen, Novae B. Simper, Charles K. Childers
Journal of Pediatric Surgery Case Reports.2016; 11: 17. CrossRef
- A case of completely isolated advanced enteric duplication cyst cancer performed partial pancreatectomy
Original Article
- Mucinous Adenocarcinoma of Anal Ducts.
- Young Ha Oh, Wan Seop Kim, Eun Kyung Hong, Moon Hyang Park, Jung Dal Lee
- Korean J Pathol. 1996;30(9):843-850.
- 2,189 View
- 43 Download
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Abstract
PDF
- Anal duct carcinoma is a rare tumor, and accounts for less than 5 percent of all anal cancers, which typically present a long-standing perianal fistulas. Some authors suggest that the fistulous tracts are congenital duplications of the lower end of the hind gut lined by rectal mucosa which is prone to malignant change to mucinous adenocarcinoma. It is usually a well differentiated mucinous (colloid) adenocarcinoma. The prognosis after wide excision of the rectum is relatively good. Since 1985, we have had three cases of anal duct carcinoma with well differentiated mucinous adenocarcinoma involving the posterior wall of the anus. Two patients had a long history of perianal fistula with mucinous discharge. There was no spread to the regional lymph node except one patient who had regional lymph node metastasis, and post-operative chemotherapy and radiation therapy were then given. All patients have no evidence of any recurrent problem at 16 months to 3 years following the surgical treatment. Because of their rarity and the failure of recognition at an early stage, we are presenting three cases to emphasize the characteristic features of this insidious, slow-growing carcinoma.
Case Reports
- Retroperitoneal Duplication Cyst Associated with Heterotopic Pancreas: A case report.
- So Yeong Oh, Myoung Ja Chung, Dong Geun Lee, Ho Yeul Choi
- Korean J Pathol. 1998;32(9):687-690.
- 1,653 View
- 10 Download
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Abstract
- Occurrence of a retroperitoneal duplication cyst associated with a heterotopic pancreas is rare. We report a case of a retroperitoneal duplication cyst associated with a heterotopic pancreas. A 35-year-old male was admitted, presenting with back pain. A pelvic computed tomographic scan disclosed a 10 cm-sized cystic mass filling the lower pelvis and displacing the rectosigmoid colon anteriorly. Histologically, the cyst wall was lined partly by mucin-secreting columnar epithelium, showing atypical hyperplasia and partly by a gastric fundic-type and a colonic-like mucosa. Beneath the epithelium, organized bundles of smooth muscle were arranged in two layers analogous to smooth muscles layers of the bowel and a small piece of pancreatic tissue were present in the smooth muscle wall of the cyst.
- Gastric Duplication Associated with Marked Atypism: A case report.
- Hae Joo Nam
- Korean J Pathol. 1999;33(1):52-54.
- 1,571 View
- 13 Download
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Abstract
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- A case of gastric duplication associated with marked atypism in an adult is reported. The patient was a 62-year-old woman presenting a mass in left upper quadrant of abdomen. The mass was a closed gastric cyst located in the greater curvature, measuring 11 9 cm in diameter. The cyst had common muscular layer with stomach. It showed gray-white firm cystic wall with yellowish brown soft necrotic tissue. Microscopically, the cyst was lined by columnar mucin-secreting epithelium having marked cellular atypism. The cyst wall was supported by layers of smooth muscle, accompanied with severe fibrosis and chronic inflammation.
Original Article
- Gastric Duplication.
- Hee Na Kim, Chang Seok Kang, Sang In Shim, Sun Moo Kim
- Korean J Pathol. 1988;22(2):148-153.
- 1,615 View
- 13 Download
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Abstract
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- Gatric duplication is a rare congenital anomaly. Thus for about 90 cases of gastric duplication have been recorded in the literature. It is less frequent than small intestinal or eosphageal duplication, and accounts for only 3.8% of all gastrointestinal tract duplication. Most gastric duplications are seen during the first year of life. Palpable abdominal mass and gastric outlet obstruction in infancy are most common presentation. We experienced a case of non-communicating gastric duplication. A 12-year-old girl visited St. Mary's Hospital because of indigestion, intermittent vomiting, and left upper quandrant pain for about 40 days. She have had intemittent abdominal pain with concomitant increased level of amylase since 5 years old. Physical examination showed a hen's egg sized palpable mass on left upper quadrant of the abdomen. Upper GI series and barium enema revealed only indentation of duodenal C-loop, and sonogram and abdominal CT demonstrated isolated cystic mass along the greater curvature of gastric antrum. She had taken an operation under the impression of pancreatic pseudocyst. Operation revealed a cystic mass, located along the greater curvature. There was no pathologic change in the pancreas. Microscopic findings of the cyst wall revealed normal gastric mucosal lining and common muscle layer, shared with gastric antral muscle layer.
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