Results 11 to 20 of about 8,307 (166)

Glomerular Capillary Microaneurysms in Membranoproliferative Glomerulonephritis: A Clinicopathological Study Highlighting the Involvement of IgG3 [PDF]

Pathol Int
Glomerular capillary microaneurysms (GCMs) were most frequently observed in proliferative glomerulonephritis with monoclonal immunoglobulin G deposits (PGNMID) among MPGN‐pattern glomerular diseases, but were not restricted to this entity. These lesions were characterized by exclusive IgG3‐dominant glomerular deposition, irrespective of light‐chain ...
Mii A, Kaneko T, Arai M, Yamada T, Takeuchi M, Kashiwagi T, Kuwahara N, Ishikawa A, Ohashi R, Sakai Y, Iwabu M, Shimizu A.   +11 more
europepmc   +2 more sources

Prevalence of membranoproliferative glomerulonephritis at Hospital General de México “Dr. Eduardo Liceaga” over a 5-year period

Revista Médica del Hospital General de México, 2017
Background: Membranoproliferative glomerulonephritis is a pattern of glomerular lesion with a variety of causes. It can be classified by using direct immunofluorescence into immune complex-mediated membranoproliferative glomerulonephritis and complement ...
C.A. Mendoza-Cerpa, M.V. Soto-Abraham
doaj   +1 more source

Membranoproliferative glomerulonephritis in Russian population [PDF]

Терапевтический архив, 2018
Aim. Analysis of etiology, clinical and morphological manifestations, approaches to therapy and prognosis of membranoproliferative glomerulonephritis (MPGN). Materials and methods.
V A Dobronravov, A V Smirnov
doaj   +1 more source

Membranoproliferative glomerulonephritis following tubulointerstitial nephritis is a late manifestation of IgG4-related kidney disease: A distinctive case

Human Pathology: Case Reports, 2019
IgG4-related kidney disease (IgG4RKD) generally presents as an active and chronic fibrosing tubulointerstitial nephritis. Recent reports have described glomerular lesions, typically with IgG4 containing subepithelial/membranous deposits as part of ...
Joichi Usui, Steven P. Salvatore, Mourhege Alsaloum, Alla Goldberg, Sheng Kuo, Surya V. Seshan   +5 more
doaj   +1 more source

Patterns of glomerular disease based on 4-year kidney biopsy material analyzed by light microscopy and immunofluorescence: a retrospective single-center analysis in Poland

Polish Journal of Pathology, 2017
The aim of this study was to assess the epidemiology of different patterns of chronic glomerular diseases based on clinical, histopathological and immunofluorescent findings of glomerulonephritis patients hospitalized in the Department of Nephrology ...
Anna Olewicz-Gawlik, Dorota Sikorska, Agnieszka Pluto-Prądzyńska, Magdalena Roszak, Ilona Idasiak-Piechocka, Krzysztof Pawlaczyk, Andrzej Oko, Aldona Woźniak, Katarzyna Iwanik, Grzegorz Dworacki, Jan Sikora, Jan Żeromski   +11 more
doaj   +1 more source

Membranoproliferative Glomerulonephritis [PDF]

, 2020
Abstract The key histological features of membranoproliferative glomerulonephritis (MPGN) are mesangial hypercellularity, endocapillary proliferation, and capillary wall remodelling. There are two main types: (1) immune complex-mediated disease—caused by chronic infection causing persistent antigenaemia (notably hepatitis C ...
Tabitha Turner-Stokes, Mark A. Little
openaire   +2 more sources

Recent advances in the diagnosis and treatment of membranoproliferative glomerulonephritis with monoclonal immunoglobulin deposition

Linchuang shenzangbing zazhi, 2022
Membranoproliferative glomerulonephritis with monoclonal immunoglobulin deposition （MPGNMID） is a rare type of monoclonal gammopathy of renal significance.
Zhang Yuan-yuan, Wang Feng-mei
doaj  

Early recurrence of proliferative glomerulonephritis with monoclonal immunoglobulin deposits in a renal allograft

Saudi Journal of Kidney Diseases and Transplantation, 2016
Proliferative glomerulonephritis with monoclonal immunoglobulin deposits (PGNMIDs) is a clinico-pathologic entity, the recurrence of which in the renal allograft has only recently been described.
Rohit Tewari, Kusum Joshi, Ashwani Kumar, C S Rayat, Rajaram Iyer, Vinay Sakhuja, Mukut Minz   +6 more
doaj   +1 more source

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

Scientific Reports, 2020
Galactose-deficient IgA1 (Gd-IgA1) is important in the pathogenesis of IgA nephropathy (IgAN). A Gd-IgA1-specific monoclonal antibody (KM55) has revealed glomerular Gd-IgA1 deposition solely in patients with IgAN and IgA vasculitis with nephritis (IgAV-N)
Shinya Ishiko, Tomoko Horinouchi, Rika Fujimaru, Yuko Shima, Hiroshi Kaito, Ryojiro Tanaka, Shingo Ishimori, Atsushi Kondo, Sadayuki Nagai, Yuya Aoto, Nana Sakakibara, China Nagano, Tomohiko Yamamura, Momoka Yoshimura, Koichi Nakanishi, Junya Fujimura, Naohiro Kamiyoshi, Hiroaki Nagase, Norishige Yoshikawa, Kazumoto Iijima, Kandai Nozu   +20 more
doaj   +1 more source

Two Cases of Membranoproliferative Glomerulonephritis With Severe Proteinuria

Journal of Behçet Uz Children's Hospital, 2019
Membranoproliferative glomerulonephritis is a common cause of chronic glomerulonephritis in older children and adolescents. Patients may present with microscopic hematuria with or without mild proteinuria with nephrotic syndrome or hypertension with ...
rahime Renda, Şenay Yıldırım, Naz Kadem, Eda Polat   +3 more
doaj   +1 more source