An extremely rare case of diphallia with high anorectal malformation with perineal lipoma
Diphallia is a very rare congenital anomalies occurs 1: 5-6 Million live birth. Associated anomalies like imperforate anus, vertebral deformities, double bladder, exstrophy of the cloacae, and duplication of the recto sigmoid may occurs in association with this. Amongst all anorectal malformations i...
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Veröffentlicht in: | Pediatric Urology Case Reports 2021-05, Vol.8 (3), p.59-61 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Diphallia is a very rare congenital anomalies occurs 1: 5-6 Million live birth. Associated anomalies like imperforate anus, vertebral deformities, double bladder, exstrophy of the cloacae, and duplication of the recto sigmoid may occurs in association with this. Amongst all anorectal malformations is a common congenital anomaly that can occur in association with diphallia. Here we are presenting a neonate with double functional penis, partial scrotal dysraphism, high anorectal malformations, presence of spina bifida occulta and a perineal lipoma successfully managed by us at our center. Key Words: Diphallia, anorectal malformations, neonate |
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ISSN: | 2148-2969 2148-2969 |
DOI: | 10.14534/j-pucr.2021267549 |