Quadricuspid Aortic Valve, Single Coronary Artery, Solitary Kidney and Oblique Facial Cleft. A Unique Constellation of Congenital Abnormalities: Case Report and Review of the Literature

2016 ◽  
Vol 7 (2) ◽  
Author(s):  
Rabah Al Mehisen ◽  
Ramy El Essely
2007 ◽  
Vol 22 (3) ◽  
pp. 235-237 ◽  
Author(s):  
Natalie F. Holt ◽  
Murali Sivarajan ◽  
Divakar Mandapati ◽  
Yevgeniy Printsev ◽  
John A. Elefteriades

2015 ◽  
Vol 25 (3) ◽  
pp. 72 ◽  
Author(s):  
Ketty Savino ◽  
Elisa Quintavalle ◽  
Giuseppe Ambrosio

2021 ◽  
Vol 27 (1) ◽  
Author(s):  
Juan Camilo Álvarez Restrepo ◽  
Susan Julieth Moreno Diaz ◽  
Sthepani Gómez Castro ◽  
Carlos Andres Riveros ◽  
Daniel Salazar Radi ◽  
...  

Abstract Background Ureteral inguinoscrotal hernias (UISH) are rare, associated in some cases with congenital abnormalities of the urinary tract. Their presentation is commonly asymptomatic, and diagnosis is mostly incidental. Case presentation A 65-year-old male patient presented to the emergency room with neurologic symptoms and an altered renal function. Further investigation revealed a ureteral paraperitoneal inguinoscrotal hernia with a pelvic ectopic solitary kidney and malrotation. Three days after hernia repair and placement of a ureteral JJ stent, the creatinine levels stabilized, and the patient was discharged. Conclusion This is the first reported case of a ureteral paraperitoneal inguinoscrotal hernia in a patient with a pelvic ectopic solitary kidney and malrotation. Currently, it is also the only case reported that has been managed by laparoscopy.


2010 ◽  
Vol 13 (3) ◽  
pp. E200-E201
Author(s):  
Amir K. Bigdeli ◽  
Eckehard Kilian ◽  
Andres Beiras-Fernandez ◽  
Ferdinand Vogt ◽  
Bruno Reichart ◽  
...  

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