Journal List > Korean J Obstet Gynecol > v.55(12) > 1088578

Park, Cho, Ji, Jeong, Chun, Jeon, and Nam: A case of prenatal diagnosis of congenital thoracic kidney in the third trimester with congenital diaphragmatic hernia

Abstract

Congenital thoracic kidney is a rare congenital malformation, caused by renal malpositioning during embryogenesis or congenital diaphregmatic hernia with herniation of kidney. Prenatal diagnosis of congenital thoracic kidney has been only rarely reported, underlying congenital diaphragmatic hernia should always be suspected in cases of congenital thoracic kidney. We present a case in which the prenatal diagnosis of an ectopic intrathoracic kidney was made on routine anatomical survey at 29 weeks' gestation.

Figures and Tables

Fig. 1
Transverse sonograms of the fetal thorax on prenatal sonographic examination at 29 weeks demonstrate the ectopic kidney (K) in the left hemithorax, compressed left lung (L), mild right shift of the heart (H).
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Fig. 2
Coronal sonographic view of the fetus. Color Doppler imaging demonstrates the left renal artery entering the thorax to feed the ectopic intrathoracic kidney (white arrow), and normal right renal artery entering the right kidney (hollowed arrow).
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Fig. 3
Intrathoracic kidney with congenital diaphragmatic hernia on postnatal X-ray (white arrows).
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Fig. 4
Left thoracic kidney on thoracoscopy (white arrows). D, diaphragm; L, left lung; K, left kidney.
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