Pseudoexstrophy associated with penile duplication and hypospadias: A case report and literature review

Bladder exstrophy is a rare developmental anomaly. Four principle variants of bladder exstrophy have been described and they themselves are rarer than the bladder exstrophy. Authors describe the management of a case of pseudoexstrophy type of variant in a 9 month old male child with penile duplication with torsion and coronal hypospadias. The rectal fascial defect was repaired without osteotomy as the distance between two pubic bones was <4 cm (3.1 cm). Genital reconstruction with excision of duplicate atrophic penile shaft and repair of coronal hypospadias with detorsion of the functional penile shaft could be accomplished. The patient had good outcome in terms of cosmesis and urinary stream. Total of 18 cases of the pseudoexstrophy have been described till date. Pseudoexstrophy of bladder is a very rare condition and can simultaneously present with other defects like omphalocele, anorectal malformations, pouch colon, multiple or solitary urogenital anomalies. The principles of correction though remain same with correction of abdominal wall defect with or without osteotomy depending upon severity of pubic diastasis. Other anomalies can undergo treatment as per standard protocol.

[1]  F. Ehsani,et al.  Pseudo-Exstrophy of Bladder with Unilateral Renal Agenesis: A Rare Combination of two Anomalies. , 2016, Journal of clinical and diagnostic research : JCDR.

[2]  R. Chadha,et al.  Congenital Pouch Colon associated with Pseudoexstrophy: Report of Two Cases , 2016, APSP journal of case reports.

[3]  A. Sudo,et al.  Staged management of pseudoexstrophy with omphalocele and wide pubic diastasis , 2014 .

[4]  J. Gearhart,et al.  Variants of the exstrophy complex: a single institution experience. , 2005, The Journal of urology.

[5]  S. Ojha,et al.  Pseudoexstrophy with Epispadias , 2005, Urologia Internationalis.

[6]  R. Hitchcock,et al.  Left-sided gastroschisis and pseudoexstrophy: a rare combination of anomalies , 2004, Pediatric Surgery International.

[7]  J. Mahajan,et al.  Pseudoexstrophy associated with megalourethra. , 2002, Journal of pediatric surgery.

[8]  J. A. Daia Fraser syndrome with bladder pseudoexstrophy. , 2001, Saudi medical journal.

[9]  L. Kasat,et al.  Pseudoexstrophy of the bladder: a rare variant , 2001, Pediatric Surgery International.

[10]  S. Pandit,et al.  Pseudoexstrophy in a female child , 2001, Indian journal of pediatrics.

[11]  D. Coplen,et al.  Congenital short colon with imperforate anus (pouch colon) , 2000, Pediatric Radiology.

[12]  J. Mahajan,et al.  Pseudoexstrophy associated with congenital pouch colon. , 1998, Journal of pediatric surgery.

[13]  R. Weiss,et al.  Pseudoexstrophy of the bladder: case report and literature review. , 1997, Journal of pediatric surgery.

[14]  R. Rızalar,et al.  A pseudoexstrophy with penile anomaly. , 1997, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

[15]  B. Churchill,et al.  Duplicate bladder exstrophy: a new variant of clinical and embryological significance. , 1990, The Journal of urology.

[16]  W. Sieber,et al.  Congenital short colon with imperforate anus: a definitive surgical cure. , 1982, Journal of pediatric surgery.

[17]  S. Živković Variations in the bladder exstrophy complex associated with large omphalocele. , 1977, The Journal of urology.

[18]  J. Johnston The genital aspects of exstrophy. , 1975, The Journal of urology.

[19]  E. Muecke,et al.  Variations in exstrophy of the bladder , 1962 .

[20]  J. H. Hejtmancik,et al.  Pseudo-exstrophy of bladder. , 1954, The Journal of urology.