scholarly journals Heterotopic gastric mucosa in jejunum: A rare case report.

JMS SKIMS ◽  
2019 ◽  
Vol 22 (1) ◽  
Author(s):  
Jan Mohammad Rather ◽  
Sobia Manzoor ◽  
Rauf Ahmad Wani
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Small Bowel ◽  
Gastric Mucosa ◽  
Rare Case ◽  
Incidental Finding ◽  
Congenital Disorder ◽  
Heterotopic Gastric Mucosa ◽  
Rare Case Report

Heterotopic gastric mucosa (HGM) has been described as an incidental finding in various parts of gastrointestinal tract. HGM of the small bowel is a congenital disorder with variable manifestations like bleeding, obstruction or perforation, penetration into adjacent organs, and fistulization. We present a case of a 55 year old female being evaluated for anemia associated with recurrent episodes of diarrhoea and dyspepsia. The cause was found to be HGM in thejejunum.

scholarly journals Mobile caecum as a content in recurrent incisional hernia an incidental finding: A rare case report

2021 ◽  
Vol 81 ◽  
pp. 105672
Author(s):  
Chinniahnapalaya Pandurangaiah Hariprasad ◽  
Rohit Gupta ◽  
Anil Kumar ◽  
Deepak Kumar Jha ◽  
Shiv Kishor ◽  
...  
Keyword(s):  
Case Report ◽  
Incisional Hernia ◽  
Rare Case ◽  
Incidental Finding ◽  
Rare Case Report

scholarly journals CASE REPORT : RARE CASE OF SMALL BOWEL OBSTRUCTION DUE TO MECKELS DIVERTICULUM

2021 ◽  
Vol 9 (06) ◽  
pp. 641-644
Author(s):  
Simranjit Kaur Dhadiala ◽  
◽  
Abhijit A. Whatkar ◽  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Rare Congenital Anomaly ◽  
Meckels Diverticulum ◽  
Male To Female

Meckels diverticulum is a rare congenital anomaly of gastrointestinal tract, seen in 2% of population. It was first described by Guilhemus Fabricus Hildonus in 1598. Meckels diverticulum is an anomaly derived from incomplete obliteration of omphalo-mesenteric duct. It is rarely seen in adults, with prevalence of male to female of 2:1. Complications associated with Meckels diverticulum are hemorrhage, inflammation and intestinal obstruction. We present to you a case of 17 year old male with unusual mechanism of small bowel obstruction due to Meckels diverticulum.

scholarly journals A Rare Case Report- An Incidental Finding of Isolated Unilocular Splenic Hydatid Cyst

2021 ◽  
pp. 259-265
Author(s):  
Shubham Satyaprakash Gupta ◽  
Sangita Jogdand Shinde ◽  
Raju K. Shinde ◽  
Shweta Pandey
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Unusual Case ◽  
Incidental Finding ◽  
Abnormal Uterine Bleeding ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Total Splenectomy ◽  
Splenic Hydatid Cyst

Splenic Hydatid Cyst is a very rare presentation with less than 5% of total incidences of Cystic Echinococcosis. It is usually due to spread of cysts from other regions leading to secondaries. Primary isolated splenic hydatid cyst without involvement of any other organs is even rarer. We report an unusual case of a female who presented as Abnormal Uterine Bleeding (AUB) with an incidental finding of Isolated Splenic Hydatid Cyst with absence of involvement of any other organ. Patient underwent laparotomy and total splenectomy was done. This case report targets to report a rare case of incidental finding of isolated unilocular hydatid cyst of spleen and describes its management.

scholarly journals Duplicated appendix with an acute abdomen in 16 years old female with both appendices inflamed: a rare case report

2020 ◽  
Vol 7 (11) ◽  
pp. 3782
Author(s):  
Shivakumar S. ◽  
Uday Kumar
Keyword(s):  
Case Report ◽  
Severe Pain ◽  
Rare Case ◽  
Incidental Finding ◽  
Iliac Fossa ◽  
Interesting Case ◽  
Ileocaecal Valve ◽  
Rare Congenital Anomaly ◽  
Pain Abdomen ◽  
Rare Case Report

Duplicated appendix is a rare congenital anomaly with incidence of 0.004-0.009% and its mostly an incidental finding on table, when one of them is acutely inflamed and very rarely both of them can be inflamed as in this case. Report a case of young girl who presented with complain of pain abdomen and vomiting in the last 2 days. Clinically patient was diagnosed to have acute appendicitis and on laparoscopy, patient had duplicated appendix one at the ileocaecal valve and the other 2cm away near the caecum with pus and faecolith. Histopathology confirmed appendicitis in the both appendices. Reported about this interesting rare case because even though the incidence of duplicated appendix is too low (0.004-0.009%), should always search for the missed appendix in patients who underwent appendicectomy earlier and complains of severe pain in right iliac fossa. Aim was to report such a rare interesting case and give a small gentle reminder to the surgeons as duplicated appendix even though rare but still a possibility.

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