Volume 1, Issue 1 (3-2015)                   CJP 2015, 1(1): 0 | Back to browse issues page

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Akhavan Sepahi M, Movahedi Z, Sadati A, Shokrollahi M R. Prenatal diagnosis and postnatal findings of cloacal malformation: a case report. CJP 2015; 1 (1) :31-34
URL: http://caspianjp.ir/article-1-30-en.html
Pediatrics Medicine Research Center , akhavansepahim@yahoo.com
Abstract:   (7805 Views)

Introduction: Cloacal malformation is an extremely rare fetal pathological condition but an important anomaly that presents as a variety of defects. It predominantly affects females, with prevalence of 1 in 50,000 births.

Prenatal ultrasonography usually showed oligohydramnios and the fetus having a large cystic mass in the lower abdomen with a single septum, bilateral hydronephrosis, ambiguous genitalia and a single umbilical artery. Postnatal finding including ambiguous genitalia and rectal atresia with a single perineal opening. 

Case report: The purpose of this case series was to illustrate characteristic prenatal sonographic features of cloacal malformation by using imaging from 3 cases seen in all academic centers to augment published data. The imaging feature common to all cases was a central cystic pelvic mass containing a characteristic fluid-fluid level.

Conclusions: The children were followed at regular intervals by an urologist, surgeon and nephrologist throughout life. Medical teams were committed to providing long-term care for children with cloacal anomalies.

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Type of Study: case report | Subject: Special

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