scholarly journals Incarcerated inguinal hernia in infancy associated with testicular infarction: Case report and review of the literature

2013 ◽  
Vol 7 (5-6) ◽  
pp. 367 ◽  
Author(s):  
Fahad Alyami ◽  
Thomas Whelan

One of the most common urgent urologic problems seen in young patients in the emergency department is the acute scrotum. Testicular infarction from an incarcerated inguinal hernia is an unusual presentation and often not considered in the initial evaluation. Herein, we present an interesting case of a 28 day old boy who presented with an acute scrotum and was found to have a testicular infarction and an incarcerated inguinal hernia. The management of similar cases in young males may vary depending on which surgical service is consulted initially and a scrotal ultrasound should be done without any delay.

2021 ◽  
Vol 2021 (2) ◽  
Author(s):  
Gregory M Taylor ◽  
Christian C Strachan

Abstract One of the most common urological emergencies encountered in pediatric patients in the emergency department (ED) is the acute scrotum. We present the case of a 4-month-old male that presented to our community ED with scrotal swelling and vomiting of 16-hours duration. He was diagnosed with a functional testicular torsion from an incarcerated inguinal hernia, transferred to a hospital with pediatric urological capabilities and was taken to the operating room ~2 hours later. His hospital course was unremarkable, and he was discharged on day 3, having made a full recovery without any loss of bowel or testicle. There have only been a handful of cases in the literature of a pediatric patient presenting with a functional testicular torsion as a result of spermatic cord compression from an indirect inguinal hernia, with no reported cases of complete salvage at nearly 18 hours since symptom onset.


2015 ◽  
Vol 2015 ◽  
pp. 1-3
Author(s):  
Reza Khorramirouz ◽  
Amin Bagheri ◽  
Alireza Aalam Sahebpour ◽  
Abdol-Mohammad Kajbafzadeh

Inguinal hernia with acute appendicitis known as Amyand’s hernia is uncommon. It may clinically manifest as acute scrotum, inguinal lymphadenitis, or strangulated hernia. The presentation of Amyand’s hernia with acute scrotum has been rarely described. Also, the manifestation of infarcted omentum in the inguinal hernia has been described in one case previously. However, the coexistence of perforated appendix with infarcted omentum in the hernia sac which manifests acute scrotum has not been described previously. Herein, we described a case of a 5-year-old boy, admitted with right tense, painful, and erythematous scrotum in the emergency room. The diagnosis of herniated appendicitis was performed preoperatively by ultrasound. Moreover, the ischemic omentum was confirmed during surgery.


2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Marc Najjar ◽  
Marc Mandel

Leiomyomas are common benign gynecologic tumors occurring in up to 30% of women. Round ligament leiomyomas however are very rare and, if symptomatic, can present as an inguinal hernia. We report the case of a 47-year-old woman who presented with an irreducible inguinal mass consistent with an incarcerated hernia. Intraoperatively, the mass was found to be a round ligament leiomyoma, a diagnosis that was confirmed by histopathology following excision of the mass. Although rare, round ligament leiomyomas should be part of the differential diagnosis of an inguinal hernia in females.


2021 ◽  
Vol 28 (4) ◽  
pp. 157-160
Author(s):  
Yoo Kyung Choi ◽  
Yo Han Ho

Testicular torsion in neonates is a urologic emergency with an incidence of 6.1 per 100,000 live births. Incarcerated inguinal hernia is also an emergency with an incidence of approximately 6% to 31% in children with inguinal hernia. Functional testicular torsion from an incarcerated inguinal hernia is a rare event in children, often not considered in the initial evaluation. A 19-day-old newborn boy was admitted to our neonatal intensive care unit after visiting a primary clinic. He presented with inconsolable crying and right scrotal swelling. Upon initial physical examination, a hard palpable mass and swelling was found in the inguinoscrotal region, accompanied with redness and warmth of the scrotum. Scrotal ultrasound with color Doppler showed inguinal hernia with strangulation and scanty blood flow to the testis. The patient underwent a right orchiectomy and partial resection of the affected small bowel. Surgical findings confirmed a testicular torsion and incarcerated inguinal hernia with testis with small bowel necrosis. Here, we report a rare case of a newborn with functional testicular torsion as a result of prolonged spermatic cord compression due to incarcerated inguinal hernia.


2020 ◽  
Vol 31 (2) ◽  
pp. 187-189
Author(s):  
AB Vico Aria ◽  
SC Alonso García ◽  
S Calzado Baeza ◽  
M Martín Díaz ◽  
F Herrera Fernández

Resumen Antecedentes: la enfermedad hidatídica es una antropozoonosis causada en la mayoría de las ocasiones por el cestodo Echinococcus granulosus (EG), caracterizada por la aparición de quistes que pueden desarrollarse en diversos órganos, fundamentalmente en hígado y pulmones. Sin embargo, la aparición de estos quistes a nivel inguinal es muy infrecuente, con muy pocos casos registrados en la literatura científica. Objetivo: presentar el caso de un paciente diagnosticado de hernia inguinal incarcerada secundaria a hidatidosis peritoneal difusa. Caso clínico: varón de 27 años e intervenido de forma urgente por tumoración inguinal irreductible y dolorosa de 24 horas de evolución. En quirófano se evidencia una hernia inguinal indirecta con presencia de saco herniario que contenía epiplón sin signos de sufrimiento y en su parte distal una tumoración, pétrea y adyacente al teste derecho, la cual fue extirpada en su totalidad. El paciente fue estudiado tras los hallazgos quirúrgicos y anatomopatológicos que informaron de lesión pseudoquística y granulomatosa, por lo que se realizó una tomografía computarizada (TC) que informó de una hidatidosis peritoneal difusa. Conclusión: la presentación de la enfermedad hidatídica peritoneal como una hernia inguinal complicada es extremadamente rara.


2021 ◽  
Vol 13 (1) ◽  
pp. 98-103
Author(s):  
Agnieszka Pawłowska-Kamieniak ◽  
Paulina Krawiec ◽  
Elżbieta Pac-Kożuchowska

Acute pancreatitis (AP) appears to be rare disease in childhood. In children, it has a different aetiology and course, and requires different management than in adult patients. The diagnosis of AP is based on at least two of the three criteria, which include typical clinical symptoms, abnormalities in laboratory tests and/or imaging studies of the pancreas. There are many known causes leading to AP in children including infections, blunt abdominal trauma, genetic factors, gallstone disease, metabolic disorders, anatomical defects of the pancreas, systemic diseases, as well as drugs, including antiepileptic drugs, and especially preparations of valproic acid. In our study, we present four cases of young patients diagnosed with acute pancreatitis as a complication of valproic acid therapy and we present a review of the literature. We believe that the activity of pancreatic enzymes should be monitored in children treated with valproate preparations in the case of clinical symptoms suggesting AP.


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