Results: 21

Stroke associated with primary membranous nephropathy in a young adult: Case report

Biomédica (Bogotá); 44 (supl.1), 2024
Introduction. Stroke in young individuals is becoming increasingly prevalent worldwide. Its causes can vary widely, so a thorough investigation by a multidisciplinary team is needed. Pinpointing the precise underlying pathology responsible for the stroke yields benefits for patients, particularly in recu...

Caracterización de enfermedades glomerulares: análisis de 22 años de biopsias renales

Rev. méd. Chile; 151 (1), 2023
BACKGROUND: The frequency of glomerular diseases is dynamic and varies according to geographic area. AIM: To evaluate the frequency of primary and secondary glomerulopathies, their demographic profile and main clinical characteristics. MATERIAL AND METHODS: Renal biopsies from native kidneys performed be...

Manejo de la nefropatía membranosa idiopática con ciclofosfamida endovenosa

Repert. med. cir; 31 (2), 2022
Introducción: las enfermedades glomerulares primarias ocupan la tercera causa de enfermedad renal crónica, siendo el origen más común de síndrome nefrótico en Colombia la nefropatía membranosa (NM). El tratamiento de la NM con ciclofosfamida endovenosa es una o...

Prevalencia del anticuerpo anti receptor de fosfolipasa A2 sérico e histológico en pacientes con nefropatía membranosa en un Centro Universitario

Rev. méd. Chile; 149 (1), 2021
BACKGROUND: The discovery of the phospholipase A2 receptor antigen and its highly specific autoantibody (anti-PLA2R Ab) was useful for the diagnosis and follow-up of patients with membranous nephropathy (MN). Thus, some international guidelines recommend not performing renal biopsy in patients with posit...

A rare case of PLA2R- and THSD7A-positive idiopathic membranous nephropathy

J. bras. nefrol; 42 (2), 2020
ABSTRACT Idiopathic membranous nephropathy (IMN) is a frequent cause of nephrotic syndrome in adults. In terms of etiology, the condition may be categorized as primary/idiopathic or secondary. Literature on the pathophysiology of IMN has indicated the presence of autoantibodies (PLA2R and THSD7A) directe...

Focal and Segmental Glomerulosclerosis and Membranous Nephropathy overlapping in a patient with Nephrotic Syndrome: a case report

J. bras. nefrol; 42 (1), 2020
Abstract Introduction: Some cases of membranous nephropathy (MGN) present focal segmental glomerulosclerosis (FSGS) typically associated with disease progression. However, we report a case of a patient who seemed to have MGN and FSGS, both primary. Case presentation: A 17-year-old female, Caucasian, pr...

Glomerulopatía membranosa con glomerulonefritis necrosante. Una asociación infrecuente

Acta méd. colomb; 44 (1), 2019
Resumen Antecedentes: la asociación entre glomerulopatía membranosa y glomerulonefritis necrosante crescéntica es infrecuente: 0.4%, confiriendo un escenario de peor pronóstico. Se requieren estudios que precisen el esquema de tratamiento óptimo, sin embargo, el rápido inicio de terapia inmunosupr...

Glomerulopatías combinadas: comunicación de 2 casos pediátricos

Arch. argent. pediatr; 116 (5), 2018
La combinación de glomerulopatías es infrecuente en la población pediátrica. Su presencia debe ser sospechada en aquellos pacientes con una enfermedad glomerular de curso clínico atípico. La influencia a largo plazo sobre el deterioro funcional renal permanece incierta. Se presentan dos niños con ...

Complement System and C4d expression in cases of Membranous nephropathy

J. bras. nefrol; 39 (4), 2017
Abstract Introduction: Membranous nephropathy (MN) is one of the major causes of nephrotic syndrome. The complement system plays a key role in the pathophysiology of MN. Objectives: To identify the complement pathway possibly activated in MN cases and correlate the presence of C4d with more severe clin...

Recovery of renal function after bilateral renal vein thrombo sis episode as complication of membranous glomerulopa thy: case report

J. bras. nefrol; 39 (4), 2017
ABSTRACT Renal vein thrombosis (RVT) is a complication often associated with nephrotic syndrome. It occurs due to a state of hypercoagulability common in the diseases that attend to this syndromic diagnosis. It should be suspected whenever there is nephrotic syndrome associated with sudden flank pain, he...