Article

Neonatal genital reconstruction in penile agenesis by anterior sagittal anorectovaginourethroplasty.

Department of Pediatric Surgery, V.S. Hospital, Ahmedabad, India.
Pediatric Surgery International (Impact Factor: 1.06). 12/2003; 19(9-10):689-92. DOI: 10.1007/s00383-003-1042-1
Source: PubMed

ABSTRACT Penile agenesis is a rare anomaly, occurring once in every 30 million births. Early gender reassignment and genital reconstruction helps the family to accept the child's altered gender and to reduce psychological problems. In the past, multiple operations were carried out to form feminized external genitalia. This report describes a single-stage gender reassignment and genital reconstruction by anterior sagittal anorectovaginourethroplasty in a neonate with penile agenesis.

1 Follower
 · 
121 Views
  • [Show abstract] [Hide abstract]
    ABSTRACT: In view of the rarity of the lesion, we describe 3 cases of aphallia associated with genitourinary and nongenitourinary anomalies. One case was associated with an anorectal malformation, whereas 2 had a normal anal opening. One patient with a normal anal opening had an associated rectal-urethro-fistula. Development of the phallus, clinical presentation of aphallia, associated anomalies, and an outline of the management is discussed along with a review of the literature.
    Journal of Pediatric Surgery 01/2010; 45(1):E13-6. DOI:10.1016/j.jpedsurg.2009.10.057 · 1.31 Impact Factor
  • Source
    [Show abstract] [Hide abstract]
    ABSTRACT: Aphallia or penile agenesis is an extremely rare congenital anomaly with an estimated incidence rate of 1 in 10 to 30 million births. We report a rare case of aphallia with right kidney hypoplasia and left kidney dysplasia in a 10-day old Iranian-Azeri male. The patient had creatinine rise and renal failure due to dysplastic left kidney and hypoplastic right kidney 􀁄􀁑􀁇􀀃􀁈􀁛􀁓􀁌􀁕􀁈􀁇􀀃􀁒􀁑􀀃􀂿􀁉􀁗􀁋􀀃􀁇􀁄􀁜􀀃􀁒􀁉􀀃􀁄􀁇􀁐􀁌􀁖􀁖􀁌􀁒􀁑􀀑􀀃􀀷􀁋􀁈􀁕􀁈􀀃􀁚􀁈􀁕􀁈􀀃􀁒􀁑􀁏􀁜􀀃 six cases of renal malformation associated with aphallia in the literature review. Three of the cases were complicated by Potter sequence and one of them was accompanied by chronic renal failure. Our case had a unique presentation because of bilateral renal malformation and subsequent renal failure without the Potter sequence.
    Archives of Iranian medicine 03/2015; 18(4):257 – 259. · 1.11 Impact Factor
  • Source
    [Show abstract] [Hide abstract]
    ABSTRACT: Aphallia or penile agenesis is an extremely rare congenital anomaly with an estimated incidence rate of 1 in 10 to 30 million births. We report a rare case of aphallia with right kidney hypoplasia and left kidney dysplasia in a 10-day old Iranian-Azeri male. The patient had creatinine rise and renal failure due to dysplastic left kidney and hypoplastic right kidney and expired on fifth day of admission. There were only six cases of renal malformation associated with aphallia in the literature review. Three of the cases were complicated by Potter sequence and one of them was accompanied by chronic renal failure. Our case had a unique presentation because of bilateral renal malformation and subsequent renal failure without the Potter sequence.
    04/2015; 18(4):257-259.

Preview

Download
0 Downloads