scholarly journals Multiple Jejunoileal Atresia and Stenosis with Duplication Cyst in a Newborn

2018 ◽  
Vol 9 (3) ◽  
pp. 19
Author(s):  
Aditya Pratap Singh ◽  
Rajlaxmi Pardeshi ◽  
Ramesh Tanger ◽  
Maryem Ansari ◽  
Arun Kumar Gupta
Keyword(s):  
Congenital Anomaly ◽  
Duplication Cyst ◽  
Mesenteric Cyst ◽  
Bilious Vomiting ◽  
Jejunoileal Atresia

Jejunoileal atresia is a congenital anomaly that is characterized clinically by bilious vomiting and abdominal dis-tension. It has been associated with various other anomalies but its association with mesenteric cyst is rare. We are presenting a patient with antenatally diagnosed duplication cyst with multiple jejunoileal atresia and stenosis with possible etiology behind such an association.

scholarly journals Importance of the Ultrasonography in Diagnosis of Ileal Duplication Cyst

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Arzu Gebesce ◽  
Mevlit Korkmaz ◽  
Esengul Keles ◽  
Feride Korkmaz ◽  
Kamran Mahmutyazıcıoglu ◽  
...  
Keyword(s):  
Ovarian Cyst ◽  
Duplication Cyst ◽  
Mesenteric Cyst ◽  
Abdominal Ultrasonography ◽  
Antenatal Ultrasonography ◽  
Mesenteric Cysts ◽  
Abdominal Mri ◽  
Double Wall ◽  
Ileal Duplication ◽  
Gastrointestinal Duplication

Gastrointestinal duplication cysts are rare congenital anomalies that can be seen in anywhere of the gastrointestinal system from the mouth to the anus. These are prenatally diagnosed through antenatal ultrasonography. However, attention must be paid since these formations might be confused with ovarian or mesenteric cysts. Our patient, who had been diagnosed with ovarian cyst on the ultrasonography performed in another center and with mesenteric cyst based on the abdominal MRI carried out at fifth month of life, presented to our clinic with the only complaint of constipation at 9th month of life. The diagnosis was set through double wall appearance of duplication cyst on the abdominal ultrasonography. The patient’s cyst was resected.

2557 Duodenal Duplication Cyst—A Rare Congenital Anomaly

2019 ◽  
Vol 114 (1) ◽  
pp. S1406-S1407
Author(s):  
Eric O. Then ◽  
Carlos Flores ◽  
Andrew Ofosu ◽  
Vijay S. Are ◽  
Andrea Culliford ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Duplication Cyst ◽  
Rare Congenital Anomaly ◽  
Duodenal Duplication ◽  
Duodenal Duplication Cyst

scholarly journals Duodenal duplication cyst presenting as bilious vomiting in a neonate

2020 ◽  
Vol 61 ◽  
pp. 101617
Author(s):  
Bakhtawar Dilawar ◽  
La-Raib Hamid ◽  
Areeba Nadeem Pirzada ◽  
Muhammad Arshad
Keyword(s):  
Duplication Cyst ◽  
Duodenal Duplication ◽  
Bilious Vomiting ◽  
Duodenal Duplication Cyst

scholarly journals Imaging Findings of Duodenal Duplication Cyst Complicated with Duodenal Intussusception and Biliary Dilatation

2016 ◽  
Vol 2016 ◽  
pp. 1-3
Author(s):  
Eduardo Torres Diez ◽  
Raúl Pellón Dabén ◽  
Juan Crespo Del Pozo ◽  
Francisco José González Sánchez
Keyword(s):  
Congenital Anomaly ◽  
Magnetic Resonance ◽  
Duplication Cyst ◽  
Imaging Findings ◽  
Rare Congenital Anomaly ◽  
Biliary Dilatation ◽  
Long Period ◽  
Duodenal Duplication ◽  
Duodenal Duplication Cyst

Duodenal duplication cyst is an extremely rare congenital anomaly usually diagnosed in childhood. However, it may remain asymptomatic for a long period. In adults it usually manifests with symptoms related to complications as pancreatitis, jaundice, or intussusception. We present the radiology findings of a patient with a duodenal intussusception secondary to a duplication cyst. The usefulness of the magnetic resonance (MR) in this case is highlighted.

scholarly journals Intraluminal pyloric duplication cyst- a rare cause of non-bilious vomiting in a neonate: A case report

2021 ◽  
Vol 10 ◽  
pp. 44
Author(s):  
Ravi Patcharu ◽  
Jaiprakash Yadav ◽  
Karunesh Chand ◽  
Badal Parikh
Keyword(s):  
Gastric Outlet Obstruction ◽  
Hypertrophic Pyloric Stenosis ◽  
Outlet Obstruction ◽  
Stable Condition ◽  
Duplication Cyst ◽  
Cystic Mass ◽  
Difficult Case ◽  
Bilious Vomiting ◽  
Recurrent Vomiting ◽  
Lesser Curvature

Background: Duplications of the alimentary tract are rare congenital malformations, out of which, true pyloric duplications constitute only 2.2%. They present with non-bilious vomiting and mimic hypertrophic pyloric stenosis (HPS). Pyloric duplications that are intraluminal are not separately visible at laparotomy, making their diagnosis difficult.  Case presentation: Our case is a neonate with an intraluminal pyloric duplication cyst who presented with recurrent vomiting. The radiological evaluation suggested a duplication cyst medial to the second part of the duodenum towards the stomach’s lesser curvature with features of gastric outlet obstruction. Intraoperatively, a cystic mass of 1 x 2 cm intraluminally was found on opening the pylorus which was excised and pyloroplasty was done. Postoperatively the baby was discharged in a stable condition. Conclusion: Intraluminal pyloric duplication cysts are rare and the clinical presentation mimics HPS. They should be considered as a differential diagnosis in a neonate presenting with features of gastric outlet obstruction.

scholarly journals Mesenteric Cyst in Association with Type-II Jejunoileal Atresia

2016 ◽  
Vol 6 (1) ◽  
pp. 17
Author(s):  
Rajat Piplani ◽  
Samir Kant Acharya ◽  
Nidhi Sugandhi ◽  
Deepak Bagga
Keyword(s):  
Rare Case ◽  
Mesenteric Cyst ◽  
Type Ii ◽  
Review Of Literature ◽  
Jejunoileal Atresia

A rare case of type-II jejunoileal atresia with mesenteric cyst in a neonate is being reported here with a brief review of literature.

scholarly journals Caecal duplication cyst: rare case report with review of literature

2019 ◽  
Vol 6 (11) ◽  
pp. 4190
Author(s):  
Muthukumaran J. ◽  
Udhayasankar V.
Keyword(s):  
Congenital Anomaly ◽  
Rare Case ◽  
Alimentary Tract ◽  
Female Child ◽  
Duplication Cyst ◽  
Paediatric Surgery ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Rare Case Report ◽  
Surgery Department

Duplication cysts of the alimentary tract are very rare congenital anomaly. Out of all these cases, two-thirds of them manifest before the age of 2 years. They are common in ileum, but very rare in cecum. We hereby report a case of 6 years female child presented in paediatric surgery department with abdominal pain, diagnosed as duplication cyst with intussusceptions.

scholarly journals A case of an abdominal wall cystic urachal carcinoma in an unusual location

2017 ◽  
Vol 4 (3) ◽  
pp. 16
Author(s):  
Kyoungyul Kim ◽  
Minsun Jung ◽  
Dongyoung Lim ◽  
Young-Joon Ryu
Keyword(s):  
Abdominal Wall ◽  
Cystic Lesion ◽  
Surgical Excision ◽  
Duplication Cyst ◽  
University Hospital ◽  
Mesenteric Cyst ◽  
Malignant Neoplasms ◽  
Regional Lymph Nodes ◽  
Urachal Carcinoma ◽  
Urachal Remnant

A solitary cystic lesion in the abdominal wall is generally benign, such as an omental cyst, mesenteric cyst, enteric duplication cyst, cystic mesothelioma, or skin appendage tumor. Furthermore, most malignancies in the urachal remnant are intraperitoneal lesions, and generally develop on the anterior aspect of the bladder dome. Moreover, most urachal glandular malignant neoplasms are the mucinous cystic type. We report a cystic urachal adenocarcinoma that presented as an abdominal wall cystic lesion. A 42-year-old woman was admitted to Kangwon National University Hospital for a 5-cm palpable abdominal wall mass. Conservative surgical excision was performed with subsequent histological and immunohistochemical evaluations, but only a few non-mucinous invasive glands and finger-like growths were noted. During a 2-year period, the tumor recurred several times along the urachal tract and metastasized to the regional lymph nodes. Despite receiving chemotherapy, the patient died 2 years after the first surgery.

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