Sjögren Syndrome-Related Membranous Glomerulonephritis Progressing to Membranoproliferative Glomerulonephritis

نویسندگان

  • Junko Yabuuchi
  • Tatsuya Suwabe
  • Toshiharu Ueno
  • Junichi Hoshino
  • Akinari Sekine
  • Noriko Hayami
  • Masahiko Oguro
  • Kyohei Kunisawa
  • Masahiro Kawada
  • Masayuki Yamanouchi
  • Keiichi Sumida
  • Hiroki Mizuno
  • Eiko Hasegawa
  • Naoki Sawa
  • Kenmei Takaichi
  • Kenichi Ohashi
  • Takeshi Fujii
  • Yoshifumi Ubara
چکیده

We report a case of glomerulopathy in a 36-year-old Japanese woman with primary Sjögren syndrome (pSS). The first renal biopsy suggested membranous glomerulonephritis. However, repeat biopsy was performed after 16 years because of increased proteinuria, revealing membranoproliferative glomerulonephritis with mesangial deposits, subendothelial deposits, and subepithelial deposits. Immunofluorescent studies showed predominant deposition of IgG2 and IgG4. This patient was positive for antinuclear antibody and anti-SS-A antibody. Sicca syndrome was confirmed by a positive Schirmer test and positive Rose Bengal test. Therefore, pSS-related glomerulopathy was considered to be the most likely diagnosis.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A Rare Case of Castleman’s Disease of Plasma Cell Type Complicated with Membranoproliferative Glomerulonephritis

Castleman’s disease (CD) is an uncommon atypical lymphoproliferative disorder with different histological and clinical forms. Patients with the plasma cell type frequently present with systemic symptoms; including fever, weight loss, hemolytic anemia, hypoalbuminemia, hypergammaglobulinemia and increased acute-phase proteins. Renal manifestations like proteinuria or hematuria are common in Cast...

متن کامل

Anti-Glomerular Basement Membrane Disease Accompanied by Membrano Proliferative Glomerulonephritis: A Case Report

Anti-glomerular basement membrane disease is characterized by autoimmunity to antigenic sites on type IV collagen of the glomerular basement membrane. The majority of patients present with rapidly progressive glomerulonephritis and alveolar hemorrhage. The occurrence of antiglomerular basement membrane disease and other types of glomerulonephritis, such as membranous nephropathy, IgA nephropath...

متن کامل

Co-existence of Type 1 Diabetes Mellitus and Nephrotic Syndrome with Membranous Glomerulonephritis in a 6 Year Old Boy: Report of a Case

Background: Nephrotic syndrome and type 1 diabetes mellitus are two common chronic conditions in children. Co-existence of these conditions is an extremely rare finding. Case presentation: This report presents a 6-year-old boy who was diagnosed with nephrotic syndrome five years ago and type 1 diabetes mellitus in infancy. Renal biopsy showed membranous glomerulonephritis, which is a rare h...

متن کامل

Clinicopathological features of atypical nephrotic syndrome in Jamaican children.

OBJECTIVES To document the histopathological spectrum of atypical nephrotic syndrome in Jamaican children and to make clinicopathological correlations which will assist physicians in identifying patients needing nephrology consultation. METHODS This was a retrospective review of renal biopsy data of Jamaican children who were referred to the University Hospital of the West Indies and the Bust...

متن کامل

Rituximab for Treatment of Membranoproliferative Glomerulonephritis and C3 Glomerulopathies

Membranoproliferative glomerulonephritis (MPGN) is a histological pattern of injury resulting from predominantly subendothelial and mesangial deposition of immunoglobulins or complement factors with subsequent inflammation and proliferation particularly of the glomerular basement membrane. Recent classification of MPGN is based on pathogenesis dividing MPGN into immunoglobulin-associated MPGN a...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2016