Abstract
Purpose: We present a series of male neonates with prenatally detected anterior urethral diverticula and discuss postnatal management. Materials and Methods: We retrospectively reviewed 3 cases of prenatally detected anterior urethral diverticula presenting between 1998 and 2005. Results: An anterior urethral cystic mass was identified prenatally in all 3 patients. One mass spontaneously ruptured prenatally. The patient underwent diverticulectomy and urethroplasty at age 6 months. Two patients had obstructive uropathy with oligohydramnios and were delivered at 32 weeks of gestation. Both cases were managed by urethrostomy and subsequent diverticulectomy and urethroplasty at age 6 months. Conclusions: Infravesical obstruction from a urethral diverticulum can be accurately identified and differentiated from other causes prenatally. Marsupialization is an excellent option for temporary urinary diversion when the clinical situation precludes primary excision and repair.
| Original language | English |
|---|---|
| Pages (from-to) | 2330-2332 |
| Number of pages | 3 |
| Journal | Journal of Urology |
| Volume | 177 |
| Issue number | 6 |
| DOIs | |
| State | Published - Jun 1 2007 |
Keywords
- diverticulum
- prenatal diagnosis
- urethra
- urethral obstruction
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