| 단독 단백뇨로 발현된 단일신의 oligomeganephronia 1례 |
| 박소은, 이정원, 조수진, 유은선, 김혜순, 성순희, 이승주 |
1이화여자대학교 의과대학 소아과학교실
2이화여자대학교 의과대학 소아과학교실
3이화여자대학교 의과대학 소아과학교실
4이화여자대학교 의과대학 소아과학교실
5이화여자대학교 의과대학 소아과학교실
6이화여자대학교 의과대학 해부병리학교실
7이화여자대학교 의과대학 소아과학교실 |
| A Case of Oligomeganephronia of the Solitary Kidney, Presented with Isolated Proteinuria |
| Soeun Park, Jung Won Lee, Su Jin Cho, Eun Sun Yoo, Hae Soon Kim, Soon Hee Sung, Seung Joo Lee |
1Department of Pediatrics, Ewha Womans University, College of Medicine
2Department of Pediatrics, Ewha Womans University, College of Medicine
3Department of Pediatrics, Ewha Womans University, College of Medicine
4Department of Pediatrics, Ewha Womans University, College of Medicine
5Department of Pediatrics, Ewha Womans University, College of Medicine
6Department of Pathology, Ewha Womans University, College of Medicine
7Department of Pediatrics, Ewha Womans University, College of Medicine |
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| ABSTRACT |
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Oligomeganephronia is rare congenital anomaly characterized by striking reduction of the number of nephrons, which are markedly hypertrophied in renal hypoplasia. Since the first description of oligomeganephronia in bilateral renal hypoplasia in 1962, dozens of cases were reported. Van Acker reported the first case of oligomeganephronia developed in the solitary kidney and 8 cases were searched in the literature. We report a case of oligomeganephronia in the solitary kidney in 13 years old boy, presented with isolated proteinuria as a first case in Korea. (J Korean Soc Pediatr Nephrol 2002 ; 6:92-6) |
| Key words:
Oligomeganephronia | Solitary kidney | Proteinuria |
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