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Fetal and Pediatric Pathology Volume 41, 2022 - Issue 2
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Case Reports

Penile Agenesis with Urethrorectal Fistula and Vesicoureteral Reflux

Oumnia BencharefFaculty of Medecine and Pharmacy of Marrakech, Pediatric Surgery, Cadi Ayyad University, Marrakech, MoroccoCorrespondence[email protected]
,
Karima FouraijiFaculty of Medecine and Pharmacy of Marrakech, Pediatric Surgery, Cadi Ayyad University, Marrakech, Morocco
,
El Ouafi El Aouni KamiliFaculty of Medecine and Pharmacy of Marrakech, Pediatric Surgery, Cadi Ayyad University, Marrakech, Morocco
&
Mohamed Oulad SaiadFaculty of Medecine and Pharmacy of Marrakech, Pediatric Surgery, Cadi Ayyad University, Marrakech, Morocco
Pages 338-340 | Received 11 May 2020, Accepted 11 Jul 2020, Published online: 13 Aug 2020
 
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Abstract

Background

Penile agenesis occurs in 1 in 30 million births. The cause of this anomaly is the failure of development of genital tubercle. Case Report: A 1-day-old neonate was born with complete penile agenesis. Imaging investigations showed an ectopic urethral insertion in the anterior wall of the rectum, and a grade 3 left vesicoureteral reflux. Conclusion: Penile agenesis is a complex genital abnormality. It can be associated with urinary malformations that should be systematically investigated.

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