A case of mesangioproliferative glomerulonephritis(GN) associated with unique lesions of juxtaglomerular apparatus (JGA) and interstitium
A case of mesangioproliferative glomerulonephritis (GN) associated with unique lesions of the juxtaglomerular apparatus (JGA) and interstitium is discussed. A 31-year-old Japanese woman who developed eyelid and pretibial edema with nephrotic-range proteinuria (4.8g/day) and without hematuria, was ad...
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Published in | Nihon Jinzo Gakkai shi Vol. 35; no. 7; pp. 869 - 873 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
Japan
Japanese Society of Nephrology
01.07.1993
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Subjects | |
Online Access | Get full text |
ISSN | 0385-2385 1884-0728 |
DOI | 10.14842/jpnjnephrol1959.35.869 |
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Abstract | A case of mesangioproliferative glomerulonephritis (GN) associated with unique lesions of the juxtaglomerular apparatus (JGA) and interstitium is discussed. A 31-year-old Japanese woman who developed eyelid and pretibial edema with nephrotic-range proteinuria (4.8g/day) and without hematuria, was admitted. Her proteinuria and edema quickly disappeared within 7 days after admission without treatment. Her blood examinations revealed hypocomplementemia on admission, but complement recovered to normal levels after 4 weeks. A renal biopsy specimen obtained on the 5th day of admission revealed moderate mesangioproliferative GN with marked periarteriolar inflammatory cell infiltrations in the JGA and occasionally in the tubular interstitium. Depositions of IgG, IgA, IgM and C3 were observed in the glomerular mesangial regions and some capillary walls, but not in the extraglomerular areas. Titers of GN-related viral antigens were not increased. Although the renal histology of this case was similar to that of experimental acute cytomegalovirus (CMV) GN in mice (described by Smith, R. D.), we could not detect CMV antigen by indirect immunofluorescent method or the virus-like particles by electron microscopy. Clinical cases of nephropathy combining lesions of the glomerulus, JGA, and intersitium are very rare. We herein report a patient with mesangioproliferative GN, who underwent an acute clinical course associated with unique inflammatory lesions of the JGA and/or interstitium. |
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AbstractList | A case of mesangioproliferative glomerulonephritis (GN) associated with unique lesions of the juxtaglomerular apparatus (JGA) and interstitium is discussed. A 31-year-old Japanese woman who developed eyelid and pretibial edema with nephrotic-range proteinuria (4.8 g/day) and without hematuria, was admitted. Her proteinuria and edema quickly disappeared within 7 days after admission without treatment. Her blood examinations revealed hypocomplementemia on admission, but complement recovered to normal levels after 4 weeks. A renal biopsy specimen obtained on the 5th day of admission revealed moderate mesangioproliferative GN with marked periarteriolar inflammatory cell infiltrations in the JGA and occasionally in the tubular interstitium. Depositions of IgG, IgA, IgM and C3 were observed in the glomerular mesangial regions and some capillary walls, but not in the extraglomerular areas. Titers of GN-related viral antigens were not increased. Although the renal histology of this case was similar to that of experimental acute cytomegalovirus (CMV) GN in mice (described by Smith, R.D.), we could not detect CMV antigen by indirect immunofluorescent method or the virus-like particles by electron microscopy. Clinical cases of nephropathy combining lesions of the glomerulus, JGA, and interstitium are very rare. We herein report a patient with mesangioproliferative GN, who underwent an acute clinical course associated with unique inflammatory lesions of the JGA and/or interstitium.A case of mesangioproliferative glomerulonephritis (GN) associated with unique lesions of the juxtaglomerular apparatus (JGA) and interstitium is discussed. A 31-year-old Japanese woman who developed eyelid and pretibial edema with nephrotic-range proteinuria (4.8 g/day) and without hematuria, was admitted. Her proteinuria and edema quickly disappeared within 7 days after admission without treatment. Her blood examinations revealed hypocomplementemia on admission, but complement recovered to normal levels after 4 weeks. A renal biopsy specimen obtained on the 5th day of admission revealed moderate mesangioproliferative GN with marked periarteriolar inflammatory cell infiltrations in the JGA and occasionally in the tubular interstitium. Depositions of IgG, IgA, IgM and C3 were observed in the glomerular mesangial regions and some capillary walls, but not in the extraglomerular areas. Titers of GN-related viral antigens were not increased. Although the renal histology of this case was similar to that of experimental acute cytomegalovirus (CMV) GN in mice (described by Smith, R.D.), we could not detect CMV antigen by indirect immunofluorescent method or the virus-like particles by electron microscopy. Clinical cases of nephropathy combining lesions of the glomerulus, JGA, and interstitium are very rare. We herein report a patient with mesangioproliferative GN, who underwent an acute clinical course associated with unique inflammatory lesions of the JGA and/or interstitium. A case of mesangioproliferative glomerulonephritis (GN) associated with unique lesions of the juxtaglomerular apparatus (JGA) and interstitium is discussed. A 31-year-old Japanese woman who developed eyelid and pretibial edema with nephrotic-range proteinuria (4.8g/day) and without hematuria, was admitted. Her proteinuria and edema quickly disappeared within 7 days after admission without treatment. Her blood examinations revealed hypocomplementemia on admission, but complement recovered to normal levels after 4 weeks. A renal biopsy specimen obtained on the 5th day of admission revealed moderate mesangioproliferative GN with marked periarteriolar inflammatory cell infiltrations in the JGA and occasionally in the tubular interstitium. Depositions of IgG, IgA, IgM and C3 were observed in the glomerular mesangial regions and some capillary walls, but not in the extraglomerular areas. Titers of GN-related viral antigens were not increased. Although the renal histology of this case was similar to that of experimental acute cytomegalovirus (CMV) GN in mice (described by Smith, R. D.), we could not detect CMV antigen by indirect immunofluorescent method or the virus-like particles by electron microscopy. Clinical cases of nephropathy combining lesions of the glomerulus, JGA, and intersitium are very rare. We herein report a patient with mesangioproliferative GN, who underwent an acute clinical course associated with unique inflammatory lesions of the JGA and/or interstitium. A case of mesangioproliferative glomerulonephritis (GN) associated with unique lesions of the juxtaglomerular apparatus (JGA) and interstitium is discussed. A 31-year-old Japanese woman who developed eyelid and pretibial edema with nephrotic-range proteinuria (4.8 g/day) and without hematuria, was admitted. Her proteinuria and edema quickly disappeared within 7 days after admission without treatment. Her blood examinations revealed hypocomplementemia on admission, but complement recovered to normal levels after 4 weeks. A renal biopsy specimen obtained on the 5th day of admission revealed moderate mesangioproliferative GN with marked periarteriolar inflammatory cell infiltrations in the JGA and occasionally in the tubular interstitium. Depositions of IgG, IgA, IgM and C3 were observed in the glomerular mesangial regions and some capillary walls, but not in the extraglomerular areas. Titers of GN-related viral antigens were not increased. Although the renal histology of this case was similar to that of experimental acute cytomegalovirus (CMV) GN in mice (described by Smith, R.D.), we could not detect CMV antigen by indirect immunofluorescent method or the virus-like particles by electron microscopy. Clinical cases of nephropathy combining lesions of the glomerulus, JGA, and interstitium are very rare. We herein report a patient with mesangioproliferative GN, who underwent an acute clinical course associated with unique inflammatory lesions of the JGA and/or interstitium. |
Author | HAYAMA, NAOAKI SHIMIZU, AKIRA TAKEUCHI, MASASHI MATSUNOBU, SEIICHI YAMANAKA, NORIAKI SAKURAI, YUSEI YONESHIMA, HIDEO KITAMURA, HIROSHI KURIHARA, SATOSHI IINO, YASUHIKO |
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References | 4) Nakada T, Shigematsu H, Bartter PC, Delea CS: Nephropathologic Characteristics of a Woman with Bartter's Syndrome after Prolonged Treatment with Spironolactone. Nephron 26: 78-84, 1980 7) Cohen AH, Nast CC: HIV-associated nephropathy: A unique combined glomerular, tubular and interstitial lesion. Mod Pathol 1: 87-97, 1988 1) Smith RD, Wehner RW: Acute Cytomegalovirus Glomerulonephritis; An Experimental Model. Lab Invest 43: 278-286, 1980 6) 鈴木 仁,加藤一夫,弓削田英知,鈴木順造:糸球体腎炎の諸型「ウィルス性腎炎」.日本臨床 46: 1289-1294, 1988 5) Michel JB, Sayah S, Guettier C, Nussberger J, Philippe M, Gonzaiez MF, Carelli C, Galen FX, Menard J, Corvol P: Physiological and Immunopathological Consequences of Active Immunization of Spontaneously Hypertensive and Normotensive Rats Against Murine Renin. Circulation 81: 1989-1910, 1990 2) Silva FG, Eigenbrodt EH, Glass M, Taft E: An Ultrastructural Study of the Renal Juxtaglomerular Apparatus and Extraglomerular Mesangium in Patients with Systemic Lupus Erythematosus. Am J Kidney Dis VII: 47-57, 1986 3) Hara M, Honda K, Matsuyama S, Endo Y, Hara S, Suzuki Y: The juxtaglomerular apparatus in IgA nephropathy; an analysis of the transport and fate of IgA deposits at the glomerular hilus. Virchows Archiv A Pathol Anat 413: 431-443, 1988 |
References_xml | – reference: 5) Michel JB, Sayah S, Guettier C, Nussberger J, Philippe M, Gonzaiez MF, Carelli C, Galen FX, Menard J, Corvol P: Physiological and Immunopathological Consequences of Active Immunization of Spontaneously Hypertensive and Normotensive Rats Against Murine Renin. Circulation 81: 1989-1910, 1990 – reference: 7) Cohen AH, Nast CC: HIV-associated nephropathy: A unique combined glomerular, tubular and interstitial lesion. Mod Pathol 1: 87-97, 1988 – reference: 3) Hara M, Honda K, Matsuyama S, Endo Y, Hara S, Suzuki Y: The juxtaglomerular apparatus in IgA nephropathy; an analysis of the transport and fate of IgA deposits at the glomerular hilus. Virchows Archiv A Pathol Anat 413: 431-443, 1988 – reference: 6) 鈴木 仁,加藤一夫,弓削田英知,鈴木順造:糸球体腎炎の諸型「ウィルス性腎炎」.日本臨床 46: 1289-1294, 1988 – reference: 4) Nakada T, Shigematsu H, Bartter PC, Delea CS: Nephropathologic Characteristics of a Woman with Bartter's Syndrome after Prolonged Treatment with Spironolactone. Nephron 26: 78-84, 1980 – reference: 2) Silva FG, Eigenbrodt EH, Glass M, Taft E: An Ultrastructural Study of the Renal Juxtaglomerular Apparatus and Extraglomerular Mesangium in Patients with Systemic Lupus Erythematosus. Am J Kidney Dis VII: 47-57, 1986 – reference: 1) Smith RD, Wehner RW: Acute Cytomegalovirus Glomerulonephritis; An Experimental Model. Lab Invest 43: 278-286, 1980 |
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SubjectTerms | Adult Antigens, Viral - blood Cell Movement Female Glomerulonephritis, Membranoproliferative - blood Glomerulonephritis, Membranoproliferative - pathology Humans Juxtaglomerular Apparatus - pathology Juxtaglomerular Apparatus - ultrastructure Mesangioproliferative glomerulonephritis, Juxtaglomerular apparatus, Interstitium, Inflammatory lesions Microscopy, Electron |
Title | A case of mesangioproliferative glomerulonephritis(GN) associated with unique lesions of juxtaglomerular apparatus (JGA) and interstitium |
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