Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios

Objective: To present female pseudohermaphroditism in a prenatally diagnosed cloacal malformation. Case report: A 29-year-old, primigravid woman referred for counseling at 17 weeks of gestation because of oligohydramnios and an intra-abdominal cyst in the fetus. The woman was not exposed to any viri...

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Main Authors: Chih-Ping Chen (Author), Chen-Yu Chen (Author), Jun-Wei Su (Author), Wayseen Wang (Author)
Format: Book
Published: Elsevier, 2013-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Chih-Ping Chen  |e author 
700 1 0 |a Chen-Yu Chen  |e author 
700 1 0 |a Jun-Wei Su  |e author 
700 1 0 |a Wayseen Wang  |e author 
245 0 0 |a Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios 
260 |b Elsevier,   |c 2013-12-01T00:00:00Z. 
500 |a 1028-4559 
500 |a 10.1016/j.tjog.2013.10.021 
520 |a Objective: To present female pseudohermaphroditism in a prenatally diagnosed cloacal malformation. Case report: A 29-year-old, primigravid woman referred for counseling at 17 weeks of gestation because of oligohydramnios and an intra-abdominal cyst in the fetus. The woman was not exposed to any virilizing agent during this pregnancy. She did not undergo any assisted reproductive technology for this pregnancy. Level II ultrasound showed a singleton with fetal biometry equivalent to 16 weeks, oligohydramnios, hydrometrocolpos, dilated bladder, and bilateral hydronephrosis. A diagnosis of cloacal malformation was made. The parents elected to terminate the pregnancy at 18 weeks of gestation. A 196-g fetus was delivered with a distended abdomen, a phallus-like structure, a small perineal opening below the phallus-like structure, and an imperforate anus. At birth, the fetus was misdiagnosed as a male with an imperforate anus and a perineal fistula. Cytogenetic analysis of the cord blood revealed a karyotype of 46,XX. Array comparative genomic hybridization analysis of the fetal tissues revealed no genomic imbalance. The phallus-like structure was an enlarged clitoris and contained accessory phallic urethra. Conclusion: Prenatal diagnosis of cloacal malformation with ambiguous genitalia should be paid attention to avoid misdiagnosis of a male with an imperforate anus and a perineal fistula. Cytogenetic analysis is helpful to determine the sex under such circumstances. 
546 |a EN 
690 |a cloacal malformation 
690 |a clitoris 
690 |a female pseudohermaphroditism 
690 |a prenatal diagnosis 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
655 7 |a article  |2 local 
786 0 |n Taiwanese Journal of Obstetrics & Gynecology, Vol 52, Iss 4, Pp 571-574 (2013) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1028455913001848 
787 0 |n https://doaj.org/toc/1028-4559 
856 4 1 |u https://doaj.org/article/4fb62c5a3a40474bafafb7dd005df6a7  |z Connect to this object online.