2011China Practical MedicineRequires access

Clinical and pathological analysis of 15 cases IgA nephropathy with manifestation of nephritic Syndrome in Children

FU Li-la

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Abstract

Objective To analyse clinncal and pathologic features of immunoglobulina nephropathy(IgAN) with manifestation of nephritic syndrome in children.Methods A retrospective review of 62 cases of primary IgAN within 6 years(2000~2006) were conducted based on renal biospy,tosummarize clinical manifestactions and pathological features of IgAN with manifestation of nephritic syndrome.Results According to WHO pathological changes of 1 case was grade II(6.7%),1 case with nephritis nephropathy;8 cases were grade III(53.3%),all cases with nephritis nephropathy.5 cases were grade IV(33.3%),2 cases with simple nephropathy,3 cases with nephritis.1 case was grade V(6.7%).Immunofluorescence typing IgA+C33 cases(20%),IgA+C3+IgG,1 case(6.7%)IgA+C3+IgG+IgM7 cases(46.7%),IgA+C3+IgM,3 cases(20%),IgA+IgM 1 case(6.7%),IgA+C3+IgG+IgM was frequently found.Conclusion The clinical representation and tissue damage of IgA nephropathy presenting with rephritic syndrome are serious,grades Ⅲ and Ⅳ.Pathologically and type IgA+C3+IgG+IgM immunologically are common.

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Objective To analyse clinncal and pathologic features of immunoglobulina nephropathy(IgAN) with manifestation of nephritic syndrome in children.Methods A retrospective review of 62 cases of primary IgAN within 6 years(2000~2006) were conducted based on renal biospy,tosummarize clinical manifestactions and pathological features of IgAN with manifestation of nephritic syndrome.Results According to WHO pathological changes of 1 case was grade II(6.7%),1 case with nephritis nephropathy;8 cases were grade III(53.3%),all cases with nephritis nephropathy.5 cases were grade IV(33.3%),2 cases with simple nephropathy,3 cases with nephritis.1 case was grade V(6.7%).Immunofluorescence typing IgA+C33 cases(20%),IgA+C3+IgG,1 case(6.7%)IgA+C3+IgG+IgM7 cases(46.7%),IgA+C3+IgM,3 cases(20%),IgA+IgM 1 case(6.7%),IgA+C3+IgG+IgM was frequently found.Conclusion The clinical representation and tissue damage of IgA nephropathy presenting with rephritic syndrome are serious,grades Ⅲ and Ⅳ.Pathologically and type IgA+C3+IgG+IgM immunologically are common.

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Available abstract

Objective To analyse clinncal and pathologic features of immunoglobulina nephropathy(IgAN) with manifestation of nephritic syndrome in children.Methods A retrospective review of 62 cases of primary IgAN within 6 years(2000~2006) were conducted based on renal biospy,tosummarize clinical manifestactions and pathological features of IgAN with manifestation of nephritic syndrome.Results According to WHO pathological changes of 1 case was grade II(6.7%),1 case with nephritis nephropathy;8 cases were grade III(53.3%),all cases with nephritis nephropathy.5 cases were grade IV(33.3%),2 cases with simple nephropathy,3 cases with nephritis.1 case was grade V(6.7%).Immunofluorescence typing IgA+C33 cases(20%),IgA+C3+IgG,1 case(6.7%)IgA+C3+IgG+IgM7 cases(46.7%),IgA+C3+IgM,3 cases(20%),IgA+IgM 1 case(6.7%),IgA+C3+IgG+IgM was frequently found.Conclusion The clinical representation and tissue damage of IgA nephropathy presenting with rephritic syndrome are serious,grades Ⅲ and Ⅳ.Pathologically and type IgA+C3+IgG+IgM immunologically are common.

Key concepts: Medicine, Nephropathy, Nephritic syndrome, Pathological, Nephritis, Glomerulonephritis, Immunoglobulin A, Immunology

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