Mesangioproliferative glomerulonephritis with IgM deposition: Clinical characteristics and outcome

被引:23
作者
Little, MA [1 ]
Dorman, A [1 ]
Gill, D [1 ]
Walshe, JJ [1 ]
机构
[1] Beaumont Hosp, Dept Nephrol, Dublin 9, Ireland
关键词
D O I
10.1081/JDI-100100886
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The significance of IgM on immunofluorescence in renal biopsy specimens remains unclear. This retrospective case study was conducted to define the clinical features, response to therapy and outcome of patients with Mesangioproliferative Glomerulonephritis (MGN) with diffuse IEM deposition. Of 1919 native renal biopsies performed over a ten-year period, 139 (7.2%) had light microscopic features of MGN and manifested IgM as the dominant immunoglobulin. When exclusion criteria (more than a trace of IgA or IgG, segmental IgM, evidence of SLE, vasculitis. FSGS or Alport's syndrome and pregnant patients) were applied, 60 patients (3.1%) remained. Follow-up data were available for 54 cases with a mean age of 26.5 years (range 1.7-63). Mean follow-up period was 7.4 years (range 4.7-22.2). Forty-one per cent presented with nephrotic syndrome (NS), 26% with asymptomatic proteinuria (>250mg/24hr), 18% with macroscopic hematuria and 15% with isolated microscopic hematuria. Twenty-one percent of patients were hypertensive at presentation. Creatinine was initially <120(mol/L in all but one patient. Only four patients (7.4%), all nephrotic, suffered a decline in renal function despite treatment; all 4 developed ESRF after a mean of 5.6 years (range 2-8.3). Two of these were subsequently re-biopsied and found to have FSGS. No patients with isolated microscopic / macroscopic hematuria or asymptomatic proteinuria suffered a decline in renal function. Protein excretion rate fell into the normal range in 63% of those receiving steroids, with 82% becoming steroid dependent. Of those treated with cyclosporine (48%) or cyclophosphamide (52%) only 9.5% and 14.5% respectively remained in prolonged remission after discontinuing treatment. Tt is concluded that MGN with IgM deposition carries a very favorable prognosis except in patients with NS who develop FSGS. However there is a high incidence of steroid dependence and resistance in the proteinuric group.
引用
收藏
页码:445 / 457
页数:13
相关论文
共 24 条
[1]   Childhood IgM nephropathy: Comparison with minimal change disease [J].
AlEisa, A ;
Carter, JE ;
Lirenman, DS ;
Magil, AB .
NEPHRON, 1996, 72 (01) :37-43
[2]  
[Anonymous], 1981, KIDNEY INT, V20, P765
[3]  
BHASIN HK, 1978, LAB INVEST, V39, P21
[4]   IMMUNOPATHOLOGIC STUDY OF MINIMAL CHANGE GLOMERULAR-DISEASE WITH MESANGIAL IGM DEPOSITS [J].
CAVALLO, T ;
JOHNSON, MP .
NEPHRON, 1981, 27 (06) :281-284
[5]  
COHEN AH, 1978, LAB INVEST, V38, P610
[6]   MONONUCLEAR CELL SUBSETS IN IGM MESANGIAL PROLIFERATIVE GLOMERULONEPHRITIS - A COMPARATIVE-STUDY WITH MINIMAL CHANGE NEPHROTIC SYNDROME AND IMMUNONEGATIVE MESANGIAL PROLIFERATIVE GLOMERULONEPHRITIS [J].
DELMORAL, RG ;
GOMEZMORALES, M ;
CORTES, V ;
AGUAYO, ML ;
GIGOSOS, RL ;
LARDELLI, P ;
NAVAS, A ;
ANEIROS, J ;
AGUILAR, D .
NEPHRON, 1993, 65 (02) :215-221
[7]   Plasmapheresis in the treatment of steroid-resistant focal segmental glomerulosclerosis in native kidneys [J].
Feld, SM ;
Figueroa, P ;
Savin, V ;
Nast, CC ;
Sharma, R ;
Sharma, M ;
Hirschberg, R ;
Adler, SG .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 32 (02) :230-237
[8]   CLINICAL-SIGNIFICANCE OF IGM MESANGIAL DEPOSITS IN THE NEPHROTIC SYNDROME [J].
GONZALO, A ;
MAMPASO, F ;
GALLEGO, N ;
QUEREDA, C ;
FIERRO, C ;
ORTUNO, J .
NEPHRON, 1985, 41 (03) :246-249
[9]  
HALL C, 1997, SOC DGH NEPHR 21 NOV
[10]   MESANGIAL PROLIFERATIVE GLOMERULONEPHRITIS WITH IGM DEPOSITS - CLINICOPATHOLOGIC ANALYSIS AND EVIDENCE FOR MORPHOLOGIC TRANSITIONS [J].
HIRSZEL, P ;
YAMASE, HT ;
CARNEY, WR ;
GALEN, MA ;
GRAEBER, CW ;
JOHNSON, KJ ;
KENNEDY, TL ;
LAPKIN, RA ;
MCLEAN, RH ;
ROSENWORCEL, E ;
ROWETT, DA .
NEPHRON, 1984, 38 (02) :100-108