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タナカ リョウジロウ
Ryojiro Tanaka
田中 亮二郎 所属 川崎医科大学 医学部 臨床医学 小児科学 職種 特任教授 |
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| 論文種別 | 原著 |
| 言語種別 | 英語 |
| 査読の有無 | 査読あり |
| 表題 | Long-term follow-up of atypical membranoproliferative glomerulonephritis: are steroids indicated? |
| 掲載誌名 | 正式名:Pediatric nephrology (Berlin, Germany) 略 称:Pediatr Nephrol ISSNコード:0931041X/0931041X |
| 掲載区分 | 国外 |
| 巻・号・頁 | 21(2),pp.194-200 |
| 著者・共著者 | Teruo Fujita, Kandai Nozu, Kazumoto Iijima, Ichiro Kamioka, Kunihiko Yoshiya, Ryojiro Tanaka, Kiyoshi Hamahira, Koichi Nakanishi, Norishige Yoshikawa, Masafumi Matsuo |
| 発行年月 | 2006/02 |
| 概要 | 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. |
| DOI | 10.1007/s00467-005-2074-7 |
| PMID | 16247645 |