Ewha Med J.  2016 Oct;39(4):118-121. 10.12771/emj.2016.39.4.118.

A Patient with IgA Nephropathy: 5 Years after Complete Remission of Minimal Change Nephrotic Syndrome

Affiliations
  • 1Department of Internal Medicine, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, Korea. wondoful1958@paik.ac.kr

Abstract

A 37-year-old male patient was admitted with generalized edema as the main symptom. A blood test confirmed hypoalbuminemia and hyperlipidemia, and a urine test confirmed severe albuminuria. A renal biopsy was conducted, which revealed a diagnosis of minimal change disease. Although the patient experienced complete remission of minimal change nephrotic syndrome after oral prednisolone and cyclophosphamide treatment, he is readmitted due to bilateral leg edema 5 years later since minimal change nephrotic syndrome was completely cured. The patient is diagnosed with IgA nephropathy. Although the exact mechanisms of IgA nephropathy in this patient remain unclear, this case represents an extremely rare development, and is separate from the remission of minimal change nephrotic syndrome.

Keyword

Nephrotic syndrome; Lipoid nephrosis; IgA glomerulonephritis

MeSH Terms

Adult
Albuminuria
Biopsy
Cyclophosphamide
Diagnosis
Edema
Glomerulonephritis, IGA*
Hematologic Tests
Humans
Hyperlipidemias
Hypoalbuminemia
Immunoglobulin A*
Leg
Male
Nephrosis, Lipoid*
Nephrotic Syndrome
Prednisolone
Cyclophosphamide
Immunoglobulin A
Prednisolone

Figure

  • Fig. 1 Renal biopsy (H&E, ×400). (A) The H&E stained section (first biopsy) shows segmental sclerosis with increased dense eosinophilic mesangial matrix. (B) The second H&E stained section (second biopsy) demonstrates mesangial expansion with foamy cell collection. (C) The last periodic acid-Schiff (PAS) stained slide shows slight mesangial proliferation.

  • Fig. 2 Electron microscope findings (×400). (A, B) Initial biopsy reveals no definite electron-dense deposits. (C) The second biopsy shows a small electron-dense deposit at the mesangium with slight mesangial proliferation.

  • Fig. 3 Immunofluorescence (×400). The IgA immunofluorescence test reveals diffuse mesangial reactivity with 3+ intensity.


Reference

1. Kikuchi M, Yumura W, Sugino N. Definition and classification of nephrotic syndrome. Nihon Rinsho. 1984; 42:1346–1351.
2. Sung JH, Hwang EA, Jin KB, Kwak JH, Han SY, Park SB, et al. Clinical pathologic study on adults idiophathic nephritic syndrome in Korea. Korean J Nephrol. 2007; 26:61–69.
3. Nolasco F, Cameron JS, Heywood EF, Hicks J, Ogg C, Williams DG. Adult-onset minimal change nephrotic syndrome: a longterm follow-up. Kidney Int. 1986; 29:1215–1223.
4. Shin YT, Oh SM, Na KR, Kim JH, Hwang PJ, Kim JS, et al. Clinical characteristics of minimal change nephrotic syndrome in adults. Korean J Nephrol. 1998; 17:46–52.
5. Fujimoto S, Yamamoto Y, Hisanaga S, Morita S, Eto T, Tanaka K. Minimal change nephrotic syndrome in adults: response to corticosteroid therapy and frequency of relapse. Am J Kidney Dis. 1991; 17:687–692.
6. Chang KJ, Park SB, Kim HC. Long-term follow-up of adultonset minimal change nephrotic syndrome. Korean J Nephrol. 2003; 22:185–194.
7. Kida H, Iida H, Dohi K, Nakamoto Y, Mizumura Y, Takeuchi J. Period of freedom from relapse as an indication of cure in minimal change nephrotic syndrome in adults. Nephron. 1977; 19:153–157.
8. Kim YS, Suh WK, Lee TW, Ihm CG, Kim MJ. Clinical characteristics and therapeutic response of adult-onset minimal change disease. Korean J Nephrol. 1987; 6:276–282.
9. Shin DH, Kim JH, Kim JY, Noh YJ, Moon SY, Kim JG, et al. A case of adult-onset minimal change nephrotic syndrome relapsed after 15-year of complete remission. Korean J Nephrol. 2003; 22:608–611.
10. Cho MH, Hong EH, Lee TH, Ko CW. Pathophysiology of minimal change nephrotic syndrome and focal segmental glomerulosclerosis. Nephrology (Carlton). 2007; 12:Suppl 3. S11–S14.
11. Barratt J, Feehally J. IgA nephropathy. J Am Soc Nephrol. 2005; 16:2088–2097.
12. Donadio JV, Grande JP. IgA nephropathy. N Engl J Med. 2002; 347:738–748.
13. Oberweis BS, Mattoo A, Wu M, Goldfarb DS. Minimal change disease and IgA deposition: separate entities or common pathophysiology? Case Rep Nephrol. 2013; 2013:268401.
Full Text Links
  • EMJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr