Literature DB >> 16937046

Spontaneous remission of therapy-resistant minimal change nephritis in an adult woman 12 years after onset of the disease.

Anton Raml1, Martin Sedlak, Bernhard Schmekal, Ulrike Stuby, Georg Syre', Georg Biesenbach.   

Abstract

A 23-year old woman was admitted to our hospital because of severe edema due to steroid resistant minimal change nephritis (MCN). The diagnosis was proven by renal biopsy nine years ago. At that time, steroid therapy led to a complete remission. Seven years later, patient was 22 years old, a relapse with severe nephrotic syndrome occurred. The diagnosis MCN was confirmed by a second renal biopsy. A combined therapy with prednisolone and cyclosporine A (CSA) led only to a partial reduction of protein excretion, the edema did not disappear. After 3 months, patient declined further therapy with CSA. On admission to our hospital, one year later in December 2000, the woman showed a severe nephrotic syndrome with edema and fluid lung, despite high doses of furosemide. Urinary protein excretion was 12.5 g/day, serum creatinine was increased to 1.4 mg/dl, the serum protein was reduced to 47 g/l. A repeated renal biopsy confirmed again the diagnosis MCN. Once again, a steroid bolus monotherapy over 4 weeks and an immunosuppressive therapy with CSA over 6 weeks had no effect on proteinuria. Further therapy regimes with mofetil mycophenolat, azathioprine, chlorambucil and cyclophosphamide over a period of 6-12 weeks of each regime was not well tolerated, proteinuria remained high with > 10 g/day. Moreover the patient suffered from severe edema despite furosemide infusions. Therefore, an additional mechanical ultrafiltration was performed 2-4 times monthly. Three months after the last immunosuppressive therapy the edema disappeared spontaneously, the diuretic therapy could be stopped. Serum creatinine was 0.8 mg/dl, protein in urine was still high with 9.8 g/day but serum protein for the first time was normal with 65 g/l. Three months later, the protein excretion was reduced to 0.48 g/l, and all other laboratory data were normal. Meanwhile, the woman has now enjoyed a complete second spontaneous remission for a period of three years.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16937046     DOI: 10.1007/s10354-005-0250-9

Source DB:  PubMed          Journal:  Wien Med Wochenschr        ISSN: 0043-5341


  16 in total

1.  Identification of an electron densification of the glomerular basement membrane in renal biopsy specimens.

Authors:  Shigeru Sato; Masamichi Ishizaki; Akira Shimizu; Mohammad Ghazizadeh; Hiroshi Kitamura; Akiko Adachi; Yoshihiro Sasaki; Wei Dai; Kyoko Wakamatsu; Yuichi Sugisaki
Journal:  Med Electron Microsc       Date:  2003-06

2.  Long-term cyclosporine therapy for pediatric nephrotic syndrome: a clinical and histologic analysis.

Authors:  M J Gregory; W E Smoyer; A Sedman; D B Kershaw; R P Valentini; K Johnson; T E Bunchman
Journal:  J Am Soc Nephrol       Date:  1996-04       Impact factor: 10.121

3.  Histopathological atlas of renal diseases: Minimal Change disease and focal glomerulosclerosis.

Authors:  Franco Ferrario; Maria Pia Rastaldi
Journal:  J Nephrol       Date:  2005 Jan-Feb       Impact factor: 3.902

4.  Long-term outcome of adult-onset minimal-change nephropathy.

Authors:  S K Mak; C D Short; N P Mallick
Journal:  Nephrol Dial Transplant       Date:  1996-11       Impact factor: 5.992

Review 5.  Is there really an increase in non-minimal change nephrotic syndrome in children?

Authors:  Guido Filler; Elizabeth Young; Pavel Geier; Blair Carpenter; Alfred Drukker; Janusz Feber
Journal:  Am J Kidney Dis       Date:  2003-12       Impact factor: 8.860

6.  Intravenous pulse cyclophosphamide--is it effective in children with steroid-resistant nephrotic syndrome?

Authors:  Hammad O Alshaya; Jaudah A Al-Maghrabi; Jameela A Kari
Journal:  Pediatr Nephrol       Date:  2003-09-17       Impact factor: 3.714

7.  Long-term ciclosporine A treatment in adults with minimal change nephrotic syndrome or focal segmental glomerulosclerosis.

Authors:  T H Ittel; W Clasen; M Fuhs; J Kindler; M J Mihatsch; H G Sieberth
Journal:  Clin Nephrol       Date:  1995-09       Impact factor: 0.975

Review 8.  Pathology of minimal change nephropathy and segmental sclerosing glomerular disorders.

Authors:  Alexander J Howie
Journal:  Nephrol Dial Transplant       Date:  2003-08       Impact factor: 5.992

Review 9.  Immune dysregulation in minimal change nephropathy.

Authors:  Peter W Mathieson
Journal:  Nephrol Dial Transplant       Date:  2003-08       Impact factor: 5.992

10.  Idiopathic minimal change nephrotic syndrome in older adults: steroid responsiveness and pattern of relapses.

Authors:  Kai-Chung Tse; Man-Fei Lam; Pok-Siu Yip; Fu-Keung Li; Bo-Ying Choy; Kar-Neng Lai; Tak-Mao Chan
Journal:  Nephrol Dial Transplant       Date:  2003-07       Impact factor: 5.992

View more
  1 in total

1.  Spontaneous remission of adult-onset minimal change nephrotic syndrome associated with influenza B infection: a case report.

Authors:  Ayumi Haruki; Eiji Ishikawa; Kan Katayama; Takayasu Ito; Takuya Hiramoto; Mika Fujimoto; Tomohiro Murata; Masaaki Ito
Journal:  BMC Nephrol       Date:  2018-07-04       Impact factor: 2.388

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.