Complete duplication of the urinary bladder: An extremely rare congenital anomaly
oleh: Vishal Gajbhiye, Sasanka Nath, Priya Ghosh, Argha Chatterjee, Dipanjan Haldar, Sukanta K Das
| Format: | Article |
|---|---|
| Diterbitkan: | Wolters Kluwer Medknow Publications 2015-01-01 |
Deskripsi
A case of complete bladder duplication with urethra duplication, diphallus, anorectal malformation and rightsided renal agensis with ipsilateral gonadal agenesisis was reported because of its rarity. Possible deranged embryology resulting in these anomalies has been reviewed with relevant hypothesis. The patient underwent several investigations and undergoing multistage surgical intervention.