scholarly journals Gastrointestinal Stromal Tumor Arising From a Gastric Duplication Cyst

2016 ◽  
Vol 3 (1) ◽  
pp. 175-177 ◽  
Author(s):  
Diego Cabrera Fernandez ◽  
Jorge Machicado ◽  
Giovanni Davogustto
Keyword(s):  
Gastrointestinal Stromal Tumor ◽  
Duplication Cyst ◽  
Stromal Tumor ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst

scholarly journals Gastric Duplication Cyst: A Rare Congenital Disease Often Misdiagnosed in Adults

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Jessica Falleti ◽  
Elena Vigliar ◽  
Pio Zeppa ◽  
Pietro Schettino ◽  
Vincenzo Napolitano ◽  
...  
Keyword(s):  
Chronic Hepatitis ◽  
Gastrointestinal Stromal Tumor ◽  
Duplication Cyst ◽  
Young Age ◽  
Stromal Tumor ◽  
Congenital Disease ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst ◽  
Gastrointestinal Duplication

Gastrointestinal duplication is a rare congenital disease which affected more commonly the ileum, while the stomach is rarely involved. Generally diagnosed in paediatric or young age, it could be difficult to suspect a gastrointestinal duplication in adults. Herein, we report a 55-year-old male with a gastric duplication cyst found on routinely checkup for chronic hepatitis and first misdiagnosed as a gastrointestinal stromal tumor (GIST); we also discuss its embryology.

Gastric Duplication Cyst Masquerading as a Gastrointestinal Stromal Tumor (GIST)

2016 ◽  
Vol 111 ◽  
pp. S1134
Author(s):  
Malav P. Parikh ◽  
Niyati Gupta ◽  
Sreelakshmi Panginikkod ◽  
Harsh Rawal ◽  
Venu Pararath Gopalakrishnan
Keyword(s):  
Gastrointestinal Stromal Tumor ◽  
Duplication Cyst ◽  
Stromal Tumor ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst

scholarly journals An Adult Gastric Duplication Cyst Mimicking a Gastrointestinal Stromal Tumor

2016 ◽  
Vol 55 (17) ◽  
pp. 2401-2404 ◽  
Author(s):  
Takenori Yoda ◽  
Makoto Furihata ◽  
Sayaka Nagao ◽  
Tomonori Wada
Keyword(s):  
Gastrointestinal Stromal Tumor ◽  
Duplication Cyst ◽  
Stromal Tumor ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst

scholarly journals Preoperative misdiagnosed gastrointestinal stromal tumor surgical “transferred” into gastric duplication cyst

2017 ◽  
Vol 74 (12) ◽  
pp. 1179-1182
Author(s):  
Ranko Lazovic ◽  
Brigita Smolovic ◽  
Ljiljana Vuckovic ◽  
Miodrag Radunovic
Keyword(s):  
Gastrointestinal Stromal Tumor ◽  
Duplication Cyst ◽  
Stromal Tumor ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst

scholarly journals A Case of Intrathoracic Gastric Duplication Cyst Detected on Prenatal Ultrasound Examination

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
Hisako Yagi ◽  
Yoshino Kinjyo ◽  
Yukiko Chinen ◽  
Hayase Nitta ◽  
Tadatsugu Kinjo ◽  
...  
Keyword(s):  
Cesarean Section ◽  
Cystic Lesion ◽  
Mass Effect ◽  
Posterior Mediastinum ◽  
Duplication Cyst ◽  
Elective Cesarean Section ◽  
Uneventful Recovery ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst ◽  
Elective Cesarean

A 37-year-old (G4P3) woman was referred to our hospital at 32 weeks of gestation for the evaluation of a fetus with an intrathoracic cystic lesion. Ultrasonography and magnetic resonance imaging revealed that a fetal cystic lesion without a mucosal layer was located in the posterior mediastinum. These findings were consistent with a bronchogenic cyst. At 38 3/7 weeks of gestation, an elective cesarean section was performed because of her previous cesarean section. A female neonate without any external anomalies, weighing 2,442 g, with Apgar scores of 8 and 9, and requiring no resuscitation was born. Four weeks after delivery, the neonate was admitted because of respiratory distress due to mass effect. At right lateral thoracotomy, a 105 × 65 mm of solitary smooth-walled cyst containing serosanguineous fluid was found in the posterior mediastinum, which was excised completely. Histologic examination revealed the diagnosis of the mediastinal gastric duplication cyst. The neonate made an uneventful recovery. Accurate diagnosis is not necessary, but detection and continuous observation are logical. Although gastric duplication, particularly intrathoracic, is a rare pathology, it should be considered in the differential diagnosis of any intrathoracic cyst.

scholarly journals Sarcomatoid Carcinoma Arising in a Gastric Duplication Cyst

2021 ◽  
Vol 8 (5) ◽  
pp. e00584
Author(s):  
Mohamed A. H. Ahmed ◽  
Kanchana Sanjeewani Liyanaarachchi ◽  
Shaun R. Preston ◽  
Madeleine Hewish ◽  
Izhar N. Bagwan
Keyword(s):  
Sarcomatoid Carcinoma ◽  
Duplication Cyst ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst

scholarly journals Gastric antral duplication cyst: A case report

2021 ◽  
Vol 61 (5) ◽  
pp. 287-90
Author(s):  
Kaniz Fathema ◽  
MD. Benzamin ◽  
Fahmida Begum ◽  
Fahmina Khanam ◽  
Md Mahamudul Hasan ◽  
...  
Keyword(s):  
Weight Loss ◽  
Alimentary Tract ◽  
Pancreatic Cyst ◽  
Clinical Course ◽  
Duplication Cyst ◽  
Ectopic Gastric Mucosa ◽  
Gi Tract ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst ◽  
Matters Of Concern

Alimentary tract duplications may be symptomatic or may be discovered incidentally. They are named for the organ with which they are associated.1 Congenital gastrointestinal (GI) tract duplication cysts are commonly located in the ileum (53%), mediastinum (18%), colon (13%), stomach (7%), duodenum (6%), rectum (4%), or oesophagus (2%)2. A single theory is insufficient to explain all types of duplications.3 Children may present with symptoms like vomiting, abdominal pain, lumps, or weight loss.4 The presence of ectopic gastric mucosa and the potential for malignancy remain matters of concern.2 Surgical management is essential for these rare cysts.5 We encountered a Bangladeshi boy with a gastric duplication cyst (GDC) that was pre-operatively diagnosed as a pancreatic cyst. A variety of imaging modalities failed to indicate GDC before the operation. Here we present the clinical course of the case and discuss the difficulties and problems in diagnosing GDC.

scholarly journals Gastric duplication cyst with localization in the pancreas in children

2020 ◽  
Vol 10 (1) ◽  
pp. 35-42
Author(s):  
Yurii Yu. Sokolov ◽  
Artem M. Efremenkov ◽  
Aleksandr P. Zykin ◽  
Elena L. Tumanova ◽  
Zhanna R. Omarova ◽  
...  
Keyword(s):  
Mucous Membrane ◽  
Clinical Observation ◽  
Abdominal Cavity ◽  
Clinical Manifestations ◽  
Duplication Cyst ◽  
The Body ◽  
Recurrent Bleeding ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst ◽  
Gastric Type

Introduction. Gastric duplication cyst is a rare clinical observation. More often, these cysts are localized in the fundus or body of the stomach and have a common muscle layers and blood supply. Even more rarely, duplication cysts are not anatomically connected to the stomach and are located in other parts of the abdominal cavity or in the retroperitoneal space. Cystic duplication of the gastrointestinal tract, which are localized in the pancreas, is extremely rare. The aim of the study is to demonstrate the possibility of using laparoscopy for this disease. Materials and methods. The paper describes three rare clinical observations of gastric duplication cyst topographically associated with the pancreas. In the first clinical observation, gastric duplication cyst was combined with mediastinal duplication cysts, an esophageal bronchial fistula, and extralobar pulmonary sequestrations. In the second observation, a duplication cyst had communication with the pancreatic duct system and was clinically manifested by recurrent bleeding. In the third case, a duplication cyst is diagnosed behind the body and tail of the pancreas. Results. In all cases, surgical treatment was carried out by the laparoscopic method, leading to complete recovery. Histological examination in all the described observations confirmed the gastric type of epithelium of the mucous membrane of the cysts. The article provides a review of the literature. Conclusion. Thus, the efficiency of laparoscopic interventions in children with gastric duplications topographically associated with the pancreas was demonstrated. The described rare clinical manifestations, a combination of defects, as well as the possible presence of heterotopy of the mucous membrane of the duplication cyst confirm the need for surgical correction of the disease.

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