Peritoneal metastatic adenocarcinoma possibly due to a gastric duplication cyst: a case report and literature review
Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare. During a routine health checkup, a 28-year-old man underwent abdominal sonography followed by computed tomography (CT) with contrast agent, which revealed a cys...
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Published in | BMC gastroenterology Vol. 14; no. 1; p. 48 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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BioMed Central
19.03.2014
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Abstract | Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare.
During a routine health checkup, a 28-year-old man underwent abdominal sonography followed by computed tomography (CT) with contrast agent, which revealed a cystic lesion with no enhancement. Laparoscopic surgery showed a 10 × 10 cm cyst adhering to the gastric corpus. However, attempts to remove the lesion en bloc were unsuccessful, and the ruptured cyst had contaminated the peritoneal cavity. Gastric duplication was diagnosed from microscopic examination of the cyst. Seven months later, the patient suffered a progressive increase in ascites, and repeated cytological analysis showed small nests of adenocarcinoma cells, with primary lesion unknown. Diagnostic laparoscopy showed multiple white nodules scattered over the surface of the liver, greater omentum, and peritoneum. Biopsy of the omental nodules confirmed adenocarcinoma, while carcinomatosis was diagnosed in the peritoneum.
Clinical presentation and chronological developments indicated that the malignancy probably originated from the gastric duplication cyst. This case highlights the importance of accurate preoperative diagnosis and optimal surgical management for gastric duplication as well as considering the potential existence of malignant transformation during surgical evaluation of adult patients with gastric duplication cysts. |
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AbstractList | Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare.BACKGROUNDGastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare.During a routine health checkup, a 28-year-old man underwent abdominal sonography followed by computed tomography (CT) with contrast agent, which revealed a cystic lesion with no enhancement. Laparoscopic surgery showed a 10 × 10 cm cyst adhering to the gastric corpus. However, attempts to remove the lesion en bloc were unsuccessful, and the ruptured cyst had contaminated the peritoneal cavity. Gastric duplication was diagnosed from microscopic examination of the cyst. Seven months later, the patient suffered a progressive increase in ascites, and repeated cytological analysis showed small nests of adenocarcinoma cells, with primary lesion unknown. Diagnostic laparoscopy showed multiple white nodules scattered over the surface of the liver, greater omentum, and peritoneum. Biopsy of the omental nodules confirmed adenocarcinoma, while carcinomatosis was diagnosed in the peritoneum.CASE PRESENTATIONDuring a routine health checkup, a 28-year-old man underwent abdominal sonography followed by computed tomography (CT) with contrast agent, which revealed a cystic lesion with no enhancement. Laparoscopic surgery showed a 10 × 10 cm cyst adhering to the gastric corpus. However, attempts to remove the lesion en bloc were unsuccessful, and the ruptured cyst had contaminated the peritoneal cavity. Gastric duplication was diagnosed from microscopic examination of the cyst. Seven months later, the patient suffered a progressive increase in ascites, and repeated cytological analysis showed small nests of adenocarcinoma cells, with primary lesion unknown. Diagnostic laparoscopy showed multiple white nodules scattered over the surface of the liver, greater omentum, and peritoneum. Biopsy of the omental nodules confirmed adenocarcinoma, while carcinomatosis was diagnosed in the peritoneum.Clinical presentation and chronological developments indicated that the malignancy probably originated from the gastric duplication cyst. This case highlights the importance of accurate preoperative diagnosis and optimal surgical management for gastric duplication as well as considering the potential existence of malignant transformation during surgical evaluation of adult patients with gastric duplication cysts.CONCLUSIONSClinical presentation and chronological developments indicated that the malignancy probably originated from the gastric duplication cyst. This case highlights the importance of accurate preoperative diagnosis and optimal surgical management for gastric duplication as well as considering the potential existence of malignant transformation during surgical evaluation of adult patients with gastric duplication cysts. Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare. During a routine health checkup, a 28-year-old man underwent abdominal sonography followed by computed tomography (CT) with contrast agent, which revealed a cystic lesion with no enhancement. Laparoscopic surgery showed a 10 × 10 cm cyst adhering to the gastric corpus. However, attempts to remove the lesion en bloc were unsuccessful, and the ruptured cyst had contaminated the peritoneal cavity. Gastric duplication was diagnosed from microscopic examination of the cyst. Seven months later, the patient suffered a progressive increase in ascites, and repeated cytological analysis showed small nests of adenocarcinoma cells, with primary lesion unknown. Diagnostic laparoscopy showed multiple white nodules scattered over the surface of the liver, greater omentum, and peritoneum. Biopsy of the omental nodules confirmed adenocarcinoma, while carcinomatosis was diagnosed in the peritoneum. Clinical presentation and chronological developments indicated that the malignancy probably originated from the gastric duplication cyst. This case highlights the importance of accurate preoperative diagnosis and optimal surgical management for gastric duplication as well as considering the potential existence of malignant transformation during surgical evaluation of adult patients with gastric duplication cysts. Doc number: 48 Abstract Background: Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare. Case presentation: During a routine health checkup, a 28-year-old man underwent abdominal sonography followed by computed tomography (CT) with contrast agent, which revealed a cystic lesion with no enhancement. Laparoscopic surgery showed a 10 × 10 cm cyst adhering to the gastric corpus. However, attempts to remove the lesion en bloc were unsuccessful, and the ruptured cyst had contaminated the peritoneal cavity. Gastric duplication was diagnosed from microscopic examination of the cyst. Seven months later, the patient suffered a progressive increase in ascites, and repeated cytological analysis showed small nests of adenocarcinoma cells, with primary lesion unknown. Diagnostic laparoscopy showed multiple white nodules scattered over the surface of the liver, greater omentum, and peritoneum. Biopsy of the omental nodules confirmed adenocarcinoma, while carcinomatosis was diagnosed in the peritoneum. Conclusions: Clinical presentation and chronological developments indicated that the malignancy probably originated from the gastric duplication cyst. This case highlights the importance of accurate preoperative diagnosis and optimal surgical management for gastric duplication as well as considering the potential existence of malignant transformation during surgical evaluation of adult patients with gastric duplication cysts. |
ArticleNumber | 48 |
Author | Wu, Jing Tai, Weiping Su, Hui Chang, Hong Lin, Xiangchun Meng, Mingming Liu, Kuiliang Liu, Hong |
AuthorAffiliation | 1 Gastroenterology Department, Beijing Shijitan Hospital, Capital Medical University, No.10 Tieyi road, Haidian, Beijing 100038, People’s Republic of China 2 Pathology Department, Beijing Shijitan Hospital, Capital Medical University, No.10 Tieyi road, Beijing, Haidian 100038, People’s Republic of China |
AuthorAffiliation_xml | – name: 2 Pathology Department, Beijing Shijitan Hospital, Capital Medical University, No.10 Tieyi road, Beijing, Haidian 100038, People’s Republic of China – name: 1 Gastroenterology Department, Beijing Shijitan Hospital, Capital Medical University, No.10 Tieyi road, Haidian, Beijing 100038, People’s Republic of China |
Author_xml | – sequence: 1 givenname: Kuiliang surname: Liu fullname: Liu, Kuiliang – sequence: 2 givenname: Xiangchun surname: Lin fullname: Lin, Xiangchun – sequence: 3 givenname: Jing surname: Wu fullname: Wu, Jing – sequence: 4 givenname: Hong surname: Liu fullname: Liu, Hong – sequence: 5 givenname: Mingming surname: Meng fullname: Meng, Mingming – sequence: 6 givenname: Hui surname: Su fullname: Su, Hui – sequence: 7 givenname: Weiping surname: Tai fullname: Tai, Weiping – sequence: 8 givenname: Hong surname: Chang fullname: Chang, Hong |
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Cites_doi | 10.1016/S0022-3468(79)80583-7 10.1007/s002470050771 10.1097/00000658-195504000-00019 10.1002/bjs.18004619904 10.1007/BF02282353 10.1016/j.gcb.2008.01.014 10.1177/1066896906295777 10.1136/jcp.2003.013946 10.1148/radiographics.13.5.8210590 10.1016/j.suronc.2012.03.002 10.1097/00005176-199802000-00018 10.1002/jso.2930500417 10.1016/0022-3468(70)90194-6 10.1055/s-2004-821043 |
ContentType | Journal Article |
Copyright | 2014 Liu et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. Copyright © 2014 Liu et al.; licensee BioMed Central Ltd. 2014 Liu et al.; licensee BioMed Central Ltd. |
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Snippet | Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare.
During a routine... Doc number: 48 Abstract Background: Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also... Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare.BACKGROUNDGastric... |
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SubjectTerms | Adenocarcinoma - pathology Adenocarcinoma - secondary Adult Case Report Cysts - congenital Cysts - diagnosis Cysts - surgery Gastroenterology Humans Male Neoplasm Seeding Peritoneal Neoplasms - pathology Peritoneal Neoplasms - secondary Stomach - abnormalities Stomach - surgery Stomach Neoplasms - pathology Tomography, X-Ray Computed |
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Title | Peritoneal metastatic adenocarcinoma possibly due to a gastric duplication cyst: a case report and literature review |
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