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 ◽  
...  
2020 ◽  
Vol 4 (1) ◽  
pp. 451-453
Author(s):  
Wasif Mohammad Ali ◽  
Sheikh Saif Alim ◽  
Atia Zaka UR Rab ◽  
Imad Ali ◽  
Meraj Ahmad

Author(s):  
Shubham Satyaprakash Gupta ◽  
Sangita Jogdand Shinde ◽  
Raju K. Shinde ◽  
Shweta Pandey

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.


2020 ◽  
Vol 7 (11) ◽  
pp. 3782
Author(s):  
Shivakumar S. ◽  
Uday Kumar

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.


2021 ◽  
Vol 10 (21) ◽  
pp. 1633-1635
Author(s):  
Raju Kamlakarao Shinde ◽  
Harsh Dinesh Bhalsod ◽  
Sangita Jogdand Shinde

Cases of renal leiomyomas are fewer than 100 in the literature and therefore possess a diagnostic challenge.1 By definition, leiomyomas are benign soft tissue neoplasms.2 that arise from smooth muscle cells.3 The most common sites of origin are the uterus, intestines and skin.4 One of the more unusual types of leiomyomas are the ones arising from the kidneys. They account for about 1.5 % benign lesions of kidneys.5 The methods of detection are through discovery during autopsy, incidental discovery during imaging or by clinical diagnosis in symptomatic lesions.6 Prevalence based on incidental finding at the time of autopsy is 4.2 - 5.2 %.7 Creating a differential diagnosis between leiomyomas and other malignant lesions is only possible by histopathological examination.8 We hereby report a case of 26-year-old female who presented with pain in abdomen and on histopathological examination was diagnosed as a case of renal leiomyoma.


JMS SKIMS ◽  
2019 ◽  
Vol 22 (1) ◽  
Author(s):  
Jan Mohammad Rather ◽  
Sobia Manzoor ◽  
Rauf Ahmad Wani

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.


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