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| 저보체혈증을 동반하지 않은 제2형 막중식성 사구체신염 1례 |
| 김양욱 , 오경석 , 김인호 , 김영훈 , 주종은 |
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| Abstract |
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Membranoproliferative glomerulonephritis (NP GN) is a rare disease and has also been known as mesangiocapillary glomerulonephritis. Lobular glome rulonephritis or chonic Hypocomplementemic glomerulonephritis. By histo pathology, MPGN is divided into type I, II and III (variant) and MPGN type II is considerably less common than type I. Most of the patientsith it pres- ent with nephrotic syndrome and sernm complement may be reduced in 70 percent af them. On electron microscopic finding, it is characterized by the pres- ence of segmental or diffuse electron dense depositis. We report a case of MPGN type II without hypocomplementemia |
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