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복막투석 환자에서 비강 내 Staphylococcus aureus의 보균과 복막염 및 출구감염증에 대한 연구
김치원 ( Chi Weon Kim ),오윤규 ( Yun Kyu Oh ),오국환 ( Kook Hwan Oh ),나기영 ( Ki Young Na ),임춘수 ( Chun Soo Lim ),김연수 ( Yon So Kim ),채동완 ( Dong Wan Chae ),안규리 ( Curie Ahn ),한진석 ( Jin Suk Han ),김성권 ( Suhng Gwon Ki 대한신장학회 2006 Kidney Research and Clinical Practice Vol.25 No.6
전은실,김정훈,소영,이상구,조윤숙,김연수,안규리,한진석,김성권,이정상,이현순 대한내과학회 1997 대한내과학회지 Vol.53 No.3S
유육종증에서 사구체신염의 발생은 매우 드물며, 가장 흔히 동반되는 막성신염도 현재까지 20예에 불과하였다. 또한 막성신염의 일부에서 신부전이 동반된 반면 적절한 치료방법은 아직 확립되지 않다. 저자들은 국내에서 유육종증에 동반된 막성신염을 처음으로 경험하였고, 스테로이드 치료후 단백뇨의 관해를 경험하였기에 문헌고찰과 함께 이를 보고하는 바이다. Glomerulonephritis associated with sarcoidosis is very rare and membranous nephropathy is known as the most common form of glomerulonephritis in sarcoidosis. There has been no report of glomerulonephritis associated with sarcoidosis yet in Korea. A 39-year-old woman was admitted to Seoul National University Hospital in July 1993 for pretibial pitting edema and foamy urine. In October 1992, she developed pretibial pitting edema and 1cm sized painless hard skin nodules on left buttock and right breast. At admission, she had nephrotic range proteinuria and right hilar mass. Renal biopsy and mediastinoscopic lymph node biopsy showed membranous nephropathy and noncaseating granulomatous inflammation. Therefore, she diagnosed as membranous nephropathy associated with sarcoidosis and treated with oral prednisolone. Hilar mass was disappeared 1 months after steroid therapy started and proteinuria decreased to nonnephrotic range 4 months later and subsided in March 1996. We report the first case in Korea who was diagnosed as membranous nephropathy associated with sarcoidosis and was responded well to steroid.