Glomerulonefritis fibrilar en paciente peruano: remisión funcional parcial tras inmunosupresión en hospital regional

ABSTRACT Introduction: Fibrillary glomerulonephritis (FGN) is a rare glomerular disease characterized by non-Congo red-reactive fibrillar deposits, diagnosed definitively by electron microscopy. Case presentation: We report a 59-year-old Peruvian male presenting with progressive renal failure and nephrotic syndrome requiring hemodialysis. Renal biopsy and electron microscopy revealed fibrillary deposits in glomeruli, mesangium, and tubules. Hepatitis C virus (HCV) serology was initially positive but active infection was excluded by negative viral load. Immunosuppressive therapy with prednisone and mycophenolate mofetil was initiated. Clinical outcome: After six months, partial renal recovery and remission of proteinuria allowed withdrawal from dialysis. At 24 months, renal function remains stable with no significant relapse. Conclusion: FGN may show favorable response to immunosuppression in selected cases without monoclonal gammopathy or active infection, highlighting the importance of early diagnosis and sustained follow-up.

Authors

Institutions

Publication Details

Journal
Revista Médica Panacea
Published
2025-08-03
DOI
https://doi.org/10.35563/rmp.v14i2.654
Primary Topic
Renal Diseases and Glomerulopathies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Glomerulonefritis fibrilar en paciente peruano: remisión funcional parcial tras inmunosupresión en hospital regional

Cesar Cruzalegui, Juan Carlos Berrocal Salcedo, Henry Wilfredo Cuba Ramos, Diana María Miserendino
Revista Médica Panacea
Renal Diseases and Glomerulopathies
article

Glomerulonefritis fibrilar en paciente peruano: remisión funcional parcial tras inmunosupresión en hospital regional

Cesar Cruzalegui, Juan Carlos Berrocal Salcedo, Henry Wilfredo Cuba Ramos, Diana María Miserendino
article en

Abstract

ABSTRACT Introduction: Fibrillary glomerulonephritis (FGN) is a rare glomerular disease characterized by non-Congo red-reactive fibrillar deposits, diagnosed definitively by electron microscopy. Case presentation: We report a 59-year-old Peruvian male presenting with progressive renal failure and nephrotic syndrome requiring hemodialysis. Renal biopsy and electron microscopy revealed fibrillary deposits in glomeruli, mesangium, and tubules. Hepatitis C virus (HCV) serology was initially positive but active infection was excluded by negative viral load. Immunosuppressive therapy with prednisone and mycophenolate mofetil was initiated. Clinical outcome: After six months, partial renal recovery and remission of proteinuria allowed withdrawal from dialysis. At 24 months, renal function remains stable with no significant relapse. Conclusion: FGN may show favorable response to immunosuppression in selected cases without monoclonal gammopathy or active infection, highlighting the importance of early diagnosis and sustained follow-up.

Revista Médica PanaceaVol. 14(2)
Fundación Centro de Estudios Infectológicos (AR), Hospital Base Guillermo Almenara Irigoyen (PE), St Martins Hospital (GB)
Openalex Percentile: Top 77%
Renal Diseases and Glomerulopathies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Glomerulonefritis fibrilar en paciente peruano: remisión funcional parcial tras inmunosupresión en hospital regional — Cesar Cruzalegui, Juan Carlos Berrocal Salcedo, et al. · Revista Médica Panacea (2025) | TGRS Research Map | TGRS