Long-term follow-up of atypical membranoproliferative glomerulonephritis: are steroids indicated?

被引:3
作者
Fujita, T
Nozu, K
Iijima, K
Kamioka, I
Yoshiya, K
Tanaka, R
Hamahira, K
Nakanishi, K
Yoshikawa, N
Matsuo, M
机构
[1] Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Natl Ctr Child Hlth & Dev, Dept Nephrol, Setagaya Ku, Tokyo, Japan
[3] Hara Genitourinary Hosp, Dept Nephrol, Kobe, Hyogo, Japan
[4] Hyogo Prefectural Kobe Childrens Hosp, Dept Nephrol, Kobe, Hyogo, Japan
[5] Himeji Red Cross Hosp, Dept Pediat, Himeji, Hyogo, Japan
[6] Wakayama Med Univ, Dept Pediat, Wakayama, Japan
关键词
angiotensin-converting enzyme inhibitors; atypical membranoproliferative glomerulonephritis; prognosis; steroid therapy; typical membranoproliferative glomerulonephritis;
D O I
10.1007/s00467-005-2074-7
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Atypical membranoproliferative glomerulonephritis (MPGN) has been reported to have a good prognosis when treated with corticosteroids. However, this recommendation is based on uncontrolled trials and is associated with many complications. The purpose of our study is to determine whether steroid therapy is indicated for atypical MPGN. The cases of seven patients with atypical MPGN are reported in this study. Urinary abnormalities of five of them were detected by urine screening at school, of two because of macrohematuria. Hypocomplementemia was noted in six patients. All but one patient were treated without corticosteroids, and five with angiotensin-converting enzyme inhibitors (ACEI) and/or the Chinese herbal medicine Sairei-to (TJ-114). One patient recovered spontaneously from proteinuria and was therefore not treated, and one who developed severe proteinuria during observation was treated with corticosteroids. After an average follow-up period of 10.0 years, five patients showed normal urinary findings, one had hematuria and one proteinuria. At the most recent follow-up, the renal function of all patients remained within the normal range, and serum C3 had returned to normal levels in five out of six. These findings suggest that the indication of steroid therapy for atypical MPGN should be re-examined, since most of the patients with atypical MPGN seem to have an excellent prognosis without treatment with corticosteroids.
引用
收藏
页码:194 / 200
页数:7
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