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Review
. 2014 Feb 19:2014:bcr2013202231.
doi: 10.1136/bcr-2013-202231.

Fetal ascites and hydrometrocolpos due to persistent urogenital sinus and cloaca: a rare congenital anomaly and review of literature

Affiliations
Review

Fetal ascites and hydrometrocolpos due to persistent urogenital sinus and cloaca: a rare congenital anomaly and review of literature

Aruna Nigam et al. BMJ Case Rep. .

Abstract

Fetal ascites can occur due to many heterogeneous disorders. Its association with hydrometrocolpos because of persistent urogenital sinus and cloaca is extremely rare. A 29-year-old primigravida presented at 32 weeks of gestation with ultrasonographic evidence of fetal ascites, a cystic pelvic mass, hydronephrosis and oligohydramnios. Fetal ascites in this case was due to fetal urine draining through fallopian tubes into the abdomen as a result of vesicovaginal fistula and distal vaginal atresia. The antenatal ultrasound results along with autopsy findings are discussed. Though rare, a persistent urogenital sinus is to be suspected in isolated fetal ascites cases where the viral tests are negative and there is no evidence of cardiac anomalies as this is a treatable anomaly if diagnosed at early gestational age.

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Figures

Figure 1
Figure 1
Antenatal ultrasound of fetus showing bilobed cystic structure in the lower abdomen with ascites.
Figure 2
Figure 2
Antenatal ultrasound of fetus showing bilobed cystic structure in the lower abdomen with dilated renal calyces.
Figure 3
Figure 3
External appearance of fetus showing enlarged abdomen, short limbs and congenital talipes varus.
Figure 4
Figure 4
Enlarged clitoris and labia with no perineal opening.
Figure 5
Figure 5
Fetal autopsy showing enlarged uterus and tubes with ascites.
Figure 6
Figure 6
Demonstration of infant feeding tube going into the cut dome of the bladder and coming out through vaginal incision.

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References

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