نتایج جستجو برای: iga glomerulonephritis

تعداد نتایج: 36253  

Journal: :Blood 2003
Shinya Kimura Akeyo Horie Yoshiyuki Hiki Chie Yamamoto Satoru Suzuki Junya Kuroda Masayo Deguchi Gen-ichi Kato Takahiro Karasuno Akira Hiraoka Toshikazu Yoshikawa Taira Maekawa

We describe herein a case of nephrotic syndrome (NS) following allogeneic bone marrow transplantation (allo-BMT) for natural killer cell leukemia/lymphoma. Histologic studies defined the diagnosis as crescentic glomerulonephritis with massive immunoglobulin A (IgA) deposition, which has never been reported in NS cases following allo-BMT. Most of the massive infiltrated cells in the interstice w...

2003
Shinya Kimura Akiyo Horie Yoshiyuki Hiki Chie Yamamoto Satoru Suzuki Junya Kuroda Masayo Deguchi Gen-ichi Kato Takahiro Karasuno Akira Hiraoka Toshikazu Yoshikawa Taira Maekawa

We describe herein a case of nephrotic syndrome (NS) following allogeneic bone marrow transplantation (allo-BMT) for natural killer cell leukemia/lymphoma. Histological studies defined the diagnosis as crescentic glomerulonephritis with massive IgA deposition, which have never been reported in NS cases following allo-BMT. A majority of the massive infiltrated cells in the interstice were CD3(+)...

Journal: :Kidney international 2006
C Izzi S Sanna-Cherchi E Prati R Belleri A Remedio R Tardanico M Foramitti S Guerini B F Viola E Movilli I Beerman R Lifton L Leone A Gharavi F Scolari

Hereditary factors are suspected to contribute to the pathogenesis of sporadic primary glomerulonephritis, but their contribution is difficult to delineate in the general population. We studied the prevalence of primary glomerulonephritis in an isolated population from the extreme northern Valtrompia valley, Northern Italy. Investigation of medical records, community urinary screening program a...

Atieh Makhlough, Seyyedeh Fatemeh Emadi tarkami

  Anderson-Fabry disease is a rare inherited X-linked lysosomal storage disease caused by deficiency of the enzyme alpha-galactosidase A. Hereby we report a 39 year old male that presented with proteinuria and edema. Histopathologic, immunofluorescence and ultrastractural examination of renal tissue were in favor  of  Fabry disease in associate with IgA nephropathy. Fabry's disease associated ...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2013
Cécile Couchoud Emmanuel Villar

1. Briganti EM, Russ GR, McNeil JJ et al. Risk of renal allograft loss from recurrent glomerulonephritis. N Engl J Med 2002; 347: 103–109 2. Odum J, Peh CA, Clarkson AR et al. Recurrent mesangial IgA nephritis following renal transplantation. Nephrol Dial Transplant 1994; 9: 309–312 3. Ortiz F, Gelpi R, Koskinen P et al. IgA nephropathy recurs early in the graft when assessed by protocol biopsy...

2010
Manuela Nebuloni Augusto Genderini Antonella Tosoni Sabrina Caruso Giovanni Barbiano di Belgiojoso

We described a 41-year-old female patient, who presented with proteinuria occurring 5 years after the onset of an undifferentiated connective tissue disease (UCTD). At renal biopsy, a pattern of focal necrotizing glomerulonephritis with mesangial and parietal deposition of the IgA, C3 and K chains was observed. Electron microscopy showed organized fibrillary deposits in mesangial, subendothelia...

Journal: :Journal of the American Society of Nephrology : JASN 2003
Elie Haddad Ivan C Moura Michelle Arcos-Fajardo Marie-Alice Macher Veronique Baudouin Corinne Alberti Chantal Loirat Renato C Monteiro Michel Peuchmaur

ABSTRACT. IgA nephropathy (IgA-N) that comprises Berger disease and Henoch-Schönlein Purpura (HSP) nephritis is defined by mesangial IgA deposits. Recently, this group has characterized a new receptor for IgA, the transferrin receptor (CD71), expressed on mesangial cells. To assess whether CD71 was involved in the pathogenesis of IgA-N, its expression was analyzed together with IgA deposits on ...

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