scholarly journals Case Report: A Rare Case of Appendicitis Incarcerated in an Inguinal Hernia in an 8 Year Old Male Child

2018 ◽  
Vol 05 (01) ◽  
Author(s):  
Evangelos Blevrakis ◽  
Sofia Xenaki ◽  
Emmanuel Chrysos
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Rare Case ◽  
Male Child

scholarly journals Strangulated internal supravesical hernia associated with left inguinal hernia: A very rare case report of acute intestinal obstruction

2021 ◽  
pp. 102393
Author(s):  
El yamine othmane ◽  
Fatimazahra Bensardi ◽  
Abdessamad majd ◽  
El Bakouri Abdelilah ◽  
Bouali Mounir ◽  
...  
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Intestinal Obstruction ◽  
Rare Case ◽  
Acute Intestinal Obstruction ◽  
Rare Case Report

scholarly journals Giant interparietal inguinal hernia with undescended testis—A Rare case report

2018 ◽  
Vol 42 ◽  
pp. 4-6
Author(s):  
Anil Kumar ◽  
Shiv Shankar Paswan ◽  
Anita Paswan ◽  
Rekha Kumari ◽  
Vimal Bhandari
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Rare Case ◽  
Undescended Testis ◽  
Rare Case Report

scholarly journals LIPOSARCOMA OF SPERMATIC CORD PRESENTING AS INDIRECT INGUINAL HERNIA- A RARE CASE REPORT

2011 ◽  
Vol 01 (01/03) ◽  
pp. 63-65
Author(s):  
Padma Shetty K. ◽  
Harish S. Permi ◽  
Michelle Mathias ◽  
Kishan Prasad ◽  
Teerthanath S. ◽  
...  
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Spermatic Cord ◽  
Rare Case ◽  
Surgical Excision ◽  
Myxoid Liposarcoma ◽  
Clinical Findings ◽  
Inguinal Region ◽  
Indirect Inguinal Hernia ◽  
Rare Case Report

AbstractLiposarcoma in the inguinal region though rare are clinically significant lesions. Preoperative diagnosis is difficult since the clinical findings are very similar to that of inguinal hernia. We report a rare case of Liposarcoma of the spermatic cord in 85 year old male, clinically diagnosed as left sided indirect inguinal hernia. Surgical excision specimen showed multiple globular lipomatous masses which were yellowish and grey tan with areas of myxoid degeneration and necrosis seen. Microscopic examination showed adipocytes arranged in lobules with numerous blood vessels, lipoblasts and myxoid stroma confirming the diagnosis of myxoid liposarcoma. He is on regular follow up since two years without any recurrence or metastasis. Our case report highlights the importance of sampling and examination of fatty masses in the inguinal region to rule out the possibility of liposarcoma as they are mistaken for lipoma at surgery.

A rare case report of corrected transposition of the great arteries in association with tuberous sclerosis and cardiac rhabdomyomas

2013 ◽  
Vol 24 (5) ◽  
pp. 955-957
Author(s):  
Rajiv Garg ◽  
Bhavesh Thakkar ◽  
Nilesh Oswal
Keyword(s):  
Case Report ◽  
Tuberous Sclerosis ◽  
Rare Case ◽  
Male Child ◽  
Rare Association ◽  
Rare Case Report ◽  
Congenitally Corrected Transposition ◽  
Corrected Transposition

AbstractThe neuro-cutaneous syndrome tuberous sclerosis is commonly associated with rhabdomyomas in various organs including the heart. We are reporting a rare case of a 7-month old male child with congenitally corrected transposition of the great arteries associated with tuberous sclerosis and cardiac rhabdomyomas. To our knowledge, this rare association has not been reported so far.

scholarly journals A rare case of Amyand’s hernia with acute appendicitis in a 69-year-old woman: a case report

2020 ◽  
Vol 2 (4) ◽  
pp. 385-387
Author(s):  
Antonio Gligorievski ◽  
◽  
◽  
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Acute Appendicitis ◽  
Rare Case ◽  
Ct Scanning ◽  
Amyand’S Hernia ◽  
Hernia Sac ◽  
History Of ◽  
The Right ◽  
Surgical Clinic

Introduction: Amyand’s hernia is an extremely rare and atypical hernia that is difficult to diagnose clinically characterized by the herniation of the appendix into the inguinal sac. The aim of this report is to describe a case of Amyand’s hernia and highlights the importance of early CT scanning in reaching the exact and early diagnosis of Amyand’s hernia. Case report: We present a rare case of a 69-year-old female patient with a history of intermittent pain in the right inguinal region is see at the emergency surgical clinic. The patient underwent a CT scan of the abdomen and a small pelvis, and an inflamed appendix was diagnosed. The inflamed appendix is herniated in the inguinal hernia sac. Computed tomography was the only modality to diagnose the hernia sac contents preoperatively. Discussion: The reported incidence of Amyand’s hernia is less than 1% of all adult inguinal hernia cases. Acute appendicitis in Amyand’s hernia is even less common, with 0,1% of all cases of acute appendicitis. This hernia may be present without symptoms until the inflammation of the appendix may lead to incarceration, strangulation, necrosis, perforation, or rupture. Early symptoms include tenderness and inguinal swelling. Conclusions: Computer tomography helps make an accurate and timely diagnosis of Amyand’s hernia, thus avoiding complications from delayed surgery.

scholarly journals Dysembryoplastic neuropithelial tumor: a rare case report

2017 ◽  
Vol 5 (5) ◽  
pp. 2270
Author(s):  
Shailesh Thanvi ◽  
Hemant Jangid ◽  
Yogi Raj Joshi
Keyword(s):  
Young Adults ◽  
Case Report ◽  
Rare Case ◽  
Male Child ◽  
Adjuvant Chemoradiotherapy ◽  
Rare Entity ◽  
Intractable Seizures ◽  
Rare Case Report ◽  
Children And Young Adults ◽  
Space Occupying Lesion

Dysembryoplastic neuropithelial tumor (DNET) is a rare recently described, benign glioneural tumor frequently associated with intractable seizures in children and young adults which is important to recognise clinically and radiologically as it is surgically curable without need for adjuvant chemoradiotherapy. We hereby present a case report of a 10year old male child who presented with intractable seizures and right parietal space occupying lesion which was diagnosed DNET radiologically, treated by microsurgical excision and confirmed histopathologically as DNET, thus emphasising multidisciplinary role in management of this rare entity.

scholarly journals Rowell Syndrome in a 4-Year-Old Male Child: A Rare Case Report

2019 ◽  
Vol 3 (7) ◽  
pp. 224-226
Author(s):  
Sukhmani Brar ◽  
Jayati Batra ◽  
Balvinder Kaur Brar
Keyword(s):  
Case Report ◽  
Erythema Multiforme ◽  
Lupus Erythematosus ◽  
Rare Case ◽  
Male Child ◽  
Disease Entity ◽  
Middle Aged ◽  
Rare Case Report

Rowell syndrome is an unusual disease entity characterized by the occurrence of erythema multiforme(EM) in association with lupus erythematosus(LE). The syndrome occurs mostly in middle aged women. We are reporting this case in a 4 year old child.

scholarly journals Left sided obstructed Amyand’s hernia: a rare case report

2019 ◽  
Vol 6 (5) ◽  
pp. 1806
Author(s):  
Akash Agrawal ◽  
Palak Vora
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Rare Case ◽  
Perforated Appendicitis ◽  
Amyand’S Hernia ◽  
Right Colon ◽  
Rare Form ◽  
Hernial Sac ◽  
Rare Case Report ◽  
The Right

Amyand's hernia is a rare form of an inguinal hernia (less than 1% of inguinal hernias) which occurs when the appendix is a part of hernial sac. Because of anatomical position of the appendix, it is most commonly found in the right sided hernial sac and it can also be accompanied by the caecum and/or right colon. In rare case, Amyand’s hernia can appear on the left side also. Here we report a case of left sided amyand’s hernia with acute perforated appendicitis in a 58 years old male patient at GMERS hospital, Dharpur, Patan, Gujarat, India.

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