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논문 기본 정보

자료유형
학술저널
저자정보
박혜미 (Department of Pediatrics Samsung Medical Center Sungkyunkwan University School of Medicine Seoul Ko) 박성원 (Department of Pediatrics Gangseo MizMedi Hospital Seoul Korea)
저널정보
조선대학교 의학연구원 Medical Biological Science and Engineering Medical Biological Science and Engineering Vol.4 No.2
발행연도
2021.1
수록면
91 - 97 (7page)

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A lot of congenital anomalies are detected in fetus and newborn through the use of prenatal and postnatal ultrasonography. This study aimed to assess the renal duplication incidences in neonates and provide solutions that would help in managing these patients. From January 1, 2001 to December 31, 2010, we retrospectively analyzed 113 patients with neonatal duplication of the renal collecting system who were diagnosed prenatally and confirmed postnatally kidney ultrasonography at single center. In this case, the duplication of the renal collecting system is the most common congenital malformation of the urinary tract with an incidence of 0.12%, which is lower than the general incidence of 1%. Out of the total 113 patients, the incomplete duplication kidney findings were 85 patients (75%) and complete duplication kidney findings were 18 patients (15.9%). As to whether they had other congenital anomalies, 13 out of 85 patients had incomplete duplication of the kidney and all of 18 patient had complete duplication of kidney. In our study, if there are no accompanying complications, we suggest that observing ultrasonography is sufficient without other evaluation to detect whether they are complete or incomplete.

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