A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency

Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastrointestinal anomalies. The penile agenesis associa...

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Main Authors:	R. El Qadiry, A. Lalaoui, H. Nassih, A. Bourrahouat, I. Ait Sab
Format:	Article
Language:	English
Published:	Hindawi Limited 2020-01-01
Series:	Case Reports in Pediatrics
Online Access:	http://dx.doi.org/10.1155/2020/8826520

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spelling	doaj-4a16687c5ee14d07bc8af5004e1cd53e2020-12-07T09:08:26ZengHindawi LimitedCase Reports in Pediatrics2090-68032090-68112020-01-01202010.1155/2020/88265208826520A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal InsufficiencyR. El Qadiry0A. Lalaoui1H. Nassih2A. Bourrahouat3I. Ait Sab4Pediatric B Department–Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, MoroccoPediatric B Department–Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, MoroccoPediatric B Department–Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, MoroccoPediatric B Department–Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, MoroccoPediatric B Department–Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, MoroccoAphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastrointestinal anomalies. The penile agenesis associated with adrenal insufficiency has never been reported in an infant. We report a rare case of a newborn that was diagnosed as a case of aphallia with vesicorectal fistula and vesicoureteral reflux, complicated by adrenal insufficiency with salt-wasting crisis.http://dx.doi.org/10.1155/2020/8826520
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	R. El Qadiry A. Lalaoui H. Nassih A. Bourrahouat I. Ait Sab
spellingShingle	R. El Qadiry A. Lalaoui H. Nassih A. Bourrahouat I. Ait Sab A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency Case Reports in Pediatrics
author_facet	R. El Qadiry A. Lalaoui H. Nassih A. Bourrahouat I. Ait Sab
author_sort	R. El Qadiry
title	A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_short	A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_full	A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_fullStr	A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_full_unstemmed	A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency
title_sort	new presentation: aphallia, vesicoureteral reflux, rectovesical fistula, and adrenal insufficiency
publisher	Hindawi Limited
series	Case Reports in Pediatrics
issn	2090-6803 2090-6811
publishDate	2020-01-01
description	Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and gastrointestinal anomalies. The penile agenesis associated with adrenal insufficiency has never been reported in an infant. We report a rare case of a newborn that was diagnosed as a case of aphallia with vesicorectal fistula and vesicoureteral reflux, complicated by adrenal insufficiency with salt-wasting crisis.
url	http://dx.doi.org/10.1155/2020/8826520
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A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency

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