Hydrocolpos should be considered systematically when an abdominopelvic cystic mass is diagnosed in a female fetus. Because the prognosis and neonatal management of isolated hydrocolpos with spontaneous resolution differs greatly from that of hydrocolpos associated with a cloacal
CASE REPORTS Case 1A 37-year-old woman with three previous normal pregnancies underwent ultrasound examination at 33 weeks' gestation. An anechoic pelvic mass of 10 × 6 × 5 cm behind the fetal bladder was seen (Figure 1a). Further examination revealed pyelectasis of the left kidney (12-mm dilatation of the renal pelvis), right kidney agenesis and a single umbilical artery. Magnetic resonance imaging (MRI) was performed at 34 weeks. T1-weighted (TORSO coil; field of view (FOV) 36 × 36; 5.0 ThK/2.5 sp; FSE TR 8000 TE 125) and T2-weighted (TORSO coil; FOV 42 × 42; 5.0 thK/0.5 sp; FSPGR/60TR 150 TE min) sequences were obtained on a Sygma 1.5-T SYS-GEMS unit, in the frontal, coronal and sagittal planes. A cystic mass between the bladder and rectum was identified, which appeared hyperintense on T2 sequences and hypointense on T1 sequences. Visualization of a fluid-filled uterus above the mass (Figure 1b) led to the diagnosis of hydrometrocolpos. Pyelectasis was thought to have resulted from compression by the cystic mass. Cloacal malformations were ruled out because the T1 sequence showed normal intrarectal meconium and neither digestive dilatation nor enterolithiasis. At 36 weeks, worsening pyelectasis prompted us to deliver the 2600-g girl by Cesarean section. She was transferred to a pediatric surgery center and the hydrocolpos resolved spontaneously on the day after delivery. Ultrasound examination revealed heterogeneous mostly fluid materials in the pelvic collection, and moderate pyelectasis of the left kidney that disappeared on day 2. The final diagnosis was hydrometrocolpos due to an imperforate hymen, and it evacuated spontaneously after birth. The infant underwent surgical intervention at 2 months of age for an ovarian hernia. Vaginoscopy at that time showed a normal vagina and a single uterine cervix, but the hymen opening was very small and difficult to see. Uterine malformation (the incidence of which is known to be increased in women with renal agenesis) could not be ruled out.
Case 2A 30-year-old woman in her first pregnancy was diagnosed with polyhydramnios at 27 weeks. No fetal abnormalities were observed, diabetes mellitus was ruled