scholarly journals Triple intussusception involving heterotopic pancreatic tissue: a case report

2009 ◽  
Vol 3 (1) ◽  
Author(s):  
N Sautot-Vial ◽  
H Steyaert
2014 ◽  
Vol 2014 ◽  
pp. 1-3
Author(s):  
Parkash Mandhan ◽  
Amer Al Saied ◽  
Mansour J. Ali

Congenital diaphragmatic hernia is a common developmental anomaly encountered by paediatric surgeons. It is known to be associated with extradiaphragmatic malformations, which include cardiac, renal, genital, and chromosomal abnormalities. Herein, we report a newborn born with concurrent congenital diaphragmatic hernia, Meckel’s diverticulum, and heterotopic pancreatic tissue. This is the first case report of such a triad with description of possible mechanisms of the development.


2014 ◽  
Vol 3 (3) ◽  
pp. 262-265 ◽  
Author(s):  
Rohit Mehra ◽  
Aswini K. Pujahari ◽  
Shyam S. Jaiswal

Suizo ◽  
2021 ◽  
Vol 36 (1) ◽  
pp. 97-103
Author(s):  
Miyuki KAINO ◽  
Seiji KAINO ◽  
Shun HATANAKA ◽  
Wakana GOMA ◽  
Eisaburo HIDEURA ◽  
...  

2020 ◽  
Vol 12 (1) ◽  
pp. 45-47
Author(s):  
Pezhman Alavinejad ◽  
Amir Hossein Sina ◽  
Damoon Dehnavi ◽  
Morteza Nayebi

Heterotopic pancreatic tissue, known as pancreatic rest, is a pancreatic tissue that lacks anatomic and vascular continuity with the main body of the pancreas. Common locations for this tissue include the stomach, duodenum, jejunum, Meckel diverticulum, and ileum. In this report, we present a case of a patient whose pancreatic rest was diagnosed primarily during the investigation of dysphagia with solid foods and it was located in the mid esophagus as an unusual location.


2021 ◽  
pp. 4-5
Author(s):  
B. Santhi ◽  
M. Annapoorani ◽  
Sharada bhavana

A Rare case of heterotopic pancreatic tissue of ileum causing acute intestinal obstruction has been described with a brief review of literature. A 42 yr old male patient presented to the emergency department with features of acute intestinal obstruction. After evaluation patient was taken up for emergency laparotomy which revealed a band to be arising from ileum. Furthermore, there was a small growth in the ileal wall at the site of origin of the band. Hence resection of the growth was done and followed by ileoileal anastomosis. Later on, histopathological examination of the growth revealed it to be heterotopic pancreatic tissue. Heterotopic pancreatic tissue is often an incidental nding encountered in upper gastrointestinal tract during endoscopy and surgeries. But Symptomatic ectopic pancreas of ileum is relatively rare and they very rarely present with acute symptoms as in this case


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