Abstract
Urethral duplication is an uncommon clinical finding, and classification systems have been described to explain the clinical findings. Urethral triplication is an extremely uncommon diagnosis, with few published case reports. We present the rare case of an infant noted to have a bifid urinary stream and found to have urethral triplication on voiding cystourethrography.
References
Effmann EL, Lebowitz RL, Colodny AH (1976) Duplication of the urethra. Radiology 119:179–185
Williams DI, Kenawi MM (1975) Urethral duplications in the male. Eur Urol 1:209–215
Psihramis KE, Colodny AH, Lebowitz RL et al (1986) Complete patent duplication of the urethra. J Urol 136:63–67
Toguri AG, Churchill BM, Rabinowitz R (1977) Y-type urethral triplication. J Urol 118:684
Zimmerman H, Mildenberger H (1980) Posterior urethral duplication and triplication in the male. J Pediatr Surg 15:212–214
Zattoni F, Gennari T, Rovasio A (1982) Y-type urethral triplication. Br J Urol 54:195
Forgaard DM, Ansell JS (1966) Trifurcation of the anterior urethra: a case report. J Urol 95:785–787
Woodhouse CR, Williams DI (1979) Duplications of the lower urinary tract. Br J Urol 51:481
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Hirselj, D.A., Lowe, G.K. & Jayanthi, V.R. Urethral triplication with meatuses terminating on the penis: a rare case presenting with bifid urinary stream. Pediatr Radiol 39, 1227–1229 (2009). https://doi.org/10.1007/s00247-009-1345-z
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DOI: https://doi.org/10.1007/s00247-009-1345-z