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.

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 Primary duodenal tuberculosis - A rare case report

2018 ◽  
Vol 8 (2) ◽  
pp. 1419-1421
Author(s):  
Mukesh Prasad Sah ◽  
Santosh Gautam ◽  
Chitra Raj Sharma ◽  
Dewan Saifuddin Ahmed
Keyword(s):  
Weight Loss ◽  
Case Report ◽  
Rare Case ◽  
Abdominal Tuberculosis ◽  
Mucosal Ulceration ◽  
Pain Abdomen ◽  
Rare Case Report ◽  
Gastroduodenal Tuberculosis ◽  
Duodenal Tuberculosis

Gastroduodenal tuberculosis is uncommon even in parts of world where tuberculosis is endemic and accounts for 2.3 % of abdominal tuberculosis. We present here a case of duodenal tuberculosis who presented with vomiting, pain abdomen and weight loss. Duodenoscopy revealed mucosal ulceration and nodularity with marked enlarged and erythematous surrounding folds. Histopathology of duodenum showed features of tuberculosis. 

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 Nevus sebaceous of Jadassohn of face with infundibular and keratinous cyst in an adolescent Arab male-a rare case report

2018 ◽  
Vol 6 (3) ◽  
pp. 1033
Author(s):  
Scott Arockia Singh M. ◽  
Paul Raphel ◽  
Sneha Devadas ◽  
Siny Vellukara Sasidharan
Keyword(s):  
Case Report ◽  
Skin Lesion ◽  
Rare Case ◽  
Medical Literature ◽  
Interesting Case ◽  
Malignant Change ◽  
Excision Biopsy ◽  
Rare Case Report ◽  
The Face ◽  
Nevus Sebaceous

Nevus Sebaceous of Jadassohn is rare hamartomatous skin lesion. We report an interesting case of an Adolescent Arab male 18yr old, who presented to us with a velvety plaque of 7cm length in his left preauricular area. Excision biopsy revealed Nevus sebaceous of Jadassohn with infundibular and keratinous cyst. The lesion is present since birth started as a tiny lesion and grown to the current size. No such large sized lesion on the face has ever been reported in the medical literature till date. We advise an early excision as they have strong potential for malignant change.

Fibromatosis of the Appendix Presenting with Right Iliac Fossa Mass: a Rare Case Report

2021 ◽  
Author(s):  
Anjali Bhartiya ◽  
Brij B. Agarwal ◽  
Neeraj Dhamija ◽  
Arupparna Sengupta
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Iliac Fossa ◽  
Rare Case Report

scholarly journals Renal Leiomyoma – A Rare Case Report

2021 ◽  
Vol 10 (21) ◽  
pp. 1633-1635
Author(s):  
Raju Kamlakarao Shinde ◽  
Harsh Dinesh Bhalsod ◽  
Sangita Jogdand Shinde
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Histopathological Examination ◽  
Incidental Finding ◽  
Benign Lesions ◽  
Diagnostic Challenge ◽  
Rare Case Report ◽  
Incidental Discovery ◽  
Malignant Lesions

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.

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